A form of malignant cancer which occurs within the eyeball.
Tumors or cancer of the EYE.
Tumors or cancer of the RETINA.
A general term for various neoplastic diseases of the lymphoid tissue.
The transparent, semigelatinous substance that fills the cavity behind the CRYSTALLINE LENS of the EYE and in front of the RETINA. It is contained in a thin hyaloid membrane and forms about four fifths of the optic globe.
A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes.
Removal of the whole or part of the vitreous body in treating endophthalmitis, diabetic retinopathy, retinal detachment, intraocular foreign bodies, and some types of glaucoma.
Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation.
The pressure of the fluids in the eye.
Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease.
Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges.
Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed)
Artificial implanted lenses.
A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes.
Insertion of an artificial lens to replace the natural CRYSTALLINE LENS after CATARACT EXTRACTION or to supplement the natural lens which is left in place.
Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES.
A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative.
Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder.
Measurement of ocular tension (INTRAOCULAR PRESSURE) with a tonometer. (Cline, et al., Dictionary of Visual Science, 4th ed)
A form of non-Hodgkin lymphoma having a usually diffuse pattern with both small and medium lymphocytes and small cleaved cells. It accounts for about 5% of adult non-Hodgkin lymphomas in the United States and Europe. The majority of mantle-cell lymphomas are associated with a t(11;14) translocation resulting in overexpression of the CYCLIN D1 gene (GENES, BCL-1).
An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed)
A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders.
A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma.
The clear, watery fluid which fills the anterior and posterior chambers of the eye. It has a refractive index lower than the crystalline lens, which it surrounds, and is involved in the metabolism of the cornea and the crystalline lens. (Cline et al., Dictionary of Visual Science, 4th ed, p319)
A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment.
B-cell lymphoid tumors that occur in association with AIDS. Patients often present with an advanced stage of disease and highly malignant subtypes including BURKITT LYMPHOMA; IMMUNOBLASTIC LARGE-CELL LYMPHOMA; PRIMARY EFFUSION LYMPHOMA; and DIFFUSE, LARGE B-CELL, LYMPHOMA. The tumors are often disseminated in unusual extranodal sites and chromosomal abnormalities are frequently present. It is likely that polyclonal B-cell lymphoproliferation in AIDS is a complex result of EBV infection, HIV antigenic stimulation, and T-cell-dependent HIV activation.
A systemic, large-cell, non-Hodgkin, malignant lymphoma characterized by cells with pleomorphic appearance and expressing the CD30 ANTIGEN. These so-called "hallmark" cells have lobulated and indented nuclei. This lymphoma is often mistaken for metastatic carcinoma and MALIGNANT HISTIOCYTOSIS.
A procedure for removal of the crystalline lens in cataract surgery in which an anterior capsulectomy is performed by means of a needle inserted through a small incision at the temporal limbus, allowing the lens contents to fall through the dilated pupil into the anterior chamber where they are broken up by the use of ultrasound and aspirated out of the eye through the incision. (Cline, et al., Dictionary of Visual Science, 4th ed & In Focus 1993;1(1):1)
The removal of a cataractous CRYSTALLINE LENS from the eye.
The space in the eye, filled with aqueous humor, bounded anteriorly by the cornea and a small portion of the sclera and posteriorly by a small portion of the ciliary body, the iris, and that part of the crystalline lens which presents through the pupil. (Cline et al., Dictionary of Visual Science, 4th ed, p109)
Glaucoma in which the angle of the anterior chamber is open and the trabecular meshwork does not encroach on the base of the iris.
A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen.
Inanimate objects that become enclosed in the eye.
The organ of sight constituting a pair of globular organs made up of a three-layered roughly spherical structure specialized for receiving and responding to light.
Clarity or sharpness of OCULAR VISION or the ability of the eye to see fine details. Visual acuity depends on the functions of RETINA, neuronal transmission, and the interpretative ability of the brain. Normal visual acuity is expressed as 20/20 indicating that one can see at 20 feet what should normally be seen at that distance. Visual acuity can also be influenced by brightness, color, and contrast.
A beta-adrenergic antagonist similar in action to PROPRANOLOL. The levo-isomer is the more active. Timolol has been proposed as an antihypertensive, antiarrhythmic, antiangina, and antiglaucoma agent. It is also used in the treatment of MIGRAINE DISORDERS and tremor.
Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection.
The white, opaque, fibrous, outer tunic of the eyeball, covering it entirely excepting the segment covered anteriorly by the cornea. It is essentially avascular but contains apertures for vessels, lymphatics, and nerves. It receives the tendons of insertion of the extraocular muscles and at the corneoscleral junction contains the canal of Schlemm. (From Cline et al., Dictionary of Visual Science, 4th ed)
The administration of substances into the eye with a hypodermic syringe.
Sterile solutions that are intended for instillation into the eye. It does not include solutions for cleaning eyeglasses or CONTACT LENS SOLUTIONS.
A ring of tissue extending from the scleral spur to the ora serrata of the RETINA. It consists of the uveal portion and the epithelial portion. The ciliary muscle is in the uveal portion and the ciliary processes are in the epithelial portion.
Malignant lymphoma characterized by the presence of immunoblasts with uniformly round-to-oval nuclei, one or more prominent nucleoli, and abundant cytoplasm. This class may be subdivided into plasmacytoid and clear-cell types based on cytoplasmic characteristics. A third category, pleomorphous, may be analogous to some of the peripheral T-cell lymphomas (LYMPHOMA, T-CELL, PERIPHERAL) recorded in both the United States and Japan.
Any surgical procedure for treatment of glaucoma by means of puncture or reshaping of the trabecular meshwork. It includes goniotomy, trabeculectomy, and laser perforation.
The most anterior portion of the uveal layer, separating the anterior chamber from the posterior. It consists of two layers - the stroma and the pigmented epithelium. Color of the iris depends on the amount of melanin in the stroma on reflection from the pigmented epithelium.
Lenses, generally made of plastic or silicone, that are implanted into the eye in front of the natural EYE LENS, by the IRIS, to improve VISION, OCULAR. These intraocular lenses are used to supplement the natural lens instead of replacing it.
A porelike structure surrounding the entire circumference of the anterior chamber through which aqueous humor circulates to the canal of Schlemm.
Presence of an intraocular lens after cataract extraction.
Abnormally low intraocular pressure often related to chronic inflammation (uveitis).
An antitumor alkaloid isolated from VINCA ROSEA. (Merck, 11th ed.)
Analogs or derivatives of prostaglandins F that do not occur naturally in the body. They do not include the product of the chemical synthesis of hormonal PGF.
The front third of the eyeball that includes the structures between the front surface of the cornea and the front of the VITREOUS BODY.
Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)

Evaluation of the reactive T-cell infiltrate in uveitis and intraocular lymphoma with flow cytometry of vitreous fluid (an American Ophthalmological Society thesis). (1/2)

PURPOSE: To describe the reactive T-cell infiltrate in uveitis and intraocular lymphoma using flow cytometry of clinical intraocular specimens acquired during diagnostic pars plana vitrectomy. METHODS: This was a retrospective review of diagnostic vitreous specimens (1992-2011) obtained at a university-based, tertiary care center. Seventy-eight patients with uveitis or lymphoma undergoing pars plana vitrectomy were selected for intraocular testing based on clinical diagnostic uncertainty. Pars plana vitrectomy with flow cytometry, gene rearrangement studies, and cytology was performed. RESULTS: T-cell infiltrates were found in all diagnostic categories with limited power to discriminate between uveitis and T-lymphocyte reactive infiltrates in response to intraocular lymphoma. Statistically significant differences by two-sample test of means between group means were found between 35 uveitis and 35 B-cell lymphoma cases for T-cell markers CD2, 3, 4, 5, and 7, but not for CD8. The CD4:CD8 ratio had a higher mean value in the uveitis group (P=.0113), and 8 T-cell lymphomas had a statistically greater number of CD3+ lymphocytes compared to uveitis (P=.0199) by two-sample test of means. Likelihood ratios were highest for CD2, CD5, CD7, CD4:CD8 ratio, CD20, and CD22. CONCLUSIONS: Discrimination between uveitis and lymphoma based on cell identification by flow cytometry was limited because of the prevalence of T lymphocytes in all diagnostic categories, emphasizing the importance of a reactive T-cell infiltrate in B-cell lymphomas, which may impede diagnosis. Flow cytometry may allow identification of more cases of T-cell lymphoma than reported when it is combined with gene rearrangement and cytology.  (+info)

Cytologic features in vitreous preparations of patients with suspicion of intraocular lymphoma. (2/2)

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Intraocular lymphoma, also known as ocular lymphoma or primary vitreoretinal lymphoma, is a rare type of malignancy that primarily affects the eye and surrounding tissues. It is a form of extranodal marginal zone B-cell lymphoma, which originates from the B-lymphocytes in the eye's immune system.

Intraocular lymphoma can be divided into two types:

1. Vitreoretinal lymphoma: This type of intraocular lymphoma involves the vitreous humor (the gel-like substance that fills the space between the lens and the retina) and the retina (the light-sensitive tissue at the back of the eye).
2. Uveal lymphoma: This type of intraocular lymphoma affects the uvea, which is made up of the iris, ciliary body, and choroid.

The symptoms of intraocular lymphoma may include blurred vision, floaters, decreased vision, and eye pain or discomfort. Diagnosis typically involves a combination of clinical examination, imaging studies (such as optical coherence tomography or OCT), and sometimes vitreous or retinal biopsy to confirm the presence of malignant cells.

Treatment for intraocular lymphoma may include systemic chemotherapy, radiation therapy, immunotherapy, or a combination of these approaches. In some cases, local treatments such as intravitreal chemotherapy or rituximab injections may be used to target the cancer cells within the eye. Regular follow-up and monitoring are essential to manage any potential recurrence or complications associated with the disease.

Eye neoplasms, also known as ocular tumors or eye cancer, refer to abnormal growths of tissue in the eye. These growths can be benign (non-cancerous) or malignant (cancerous). Eye neoplasms can develop in various parts of the eye, including the eyelid, conjunctiva, cornea, iris, ciliary body, choroid, retina, and optic nerve.

Benign eye neoplasms are typically slow-growing and do not spread to other parts of the body. They may cause symptoms such as vision changes, eye pain, or a noticeable mass in the eye. Treatment options for benign eye neoplasms include monitoring, surgical removal, or radiation therapy.

Malignant eye neoplasms, on the other hand, can grow and spread rapidly to other parts of the body. They may cause symptoms such as vision changes, eye pain, floaters, or flashes of light. Treatment options for malignant eye neoplasms depend on the type and stage of cancer but may include surgery, radiation therapy, chemotherapy, or a combination of these treatments.

It is important to note that early detection and treatment of eye neoplasms can improve outcomes and prevent complications. Regular eye exams with an ophthalmologist are recommended for early detection and prevention of eye diseases, including eye neoplasms.

Retinal neoplasms are abnormal growths or tumors that develop in the retina, which is the light-sensitive tissue located at the back of the eye. These neoplasms can be benign or malignant and can have varying effects on vision depending on their size, location, and type.

Retinal neoplasms can be classified into two main categories: primary and secondary. Primary retinal neoplasms originate from the retina or its surrounding tissues, while secondary retinal neoplasms spread to the retina from other parts of the body.

The most common type of primary retinal neoplasm is a retinoblastoma, which is a malignant tumor that typically affects children under the age of five. Other types of primary retinal neoplasms include capillary hemangioma, cavernous hemangioma, and combined hamartoma of the retina and RPE (retinal pigment epithelium).

Secondary retinal neoplasms are usually metastatic tumors that spread to the eye from other parts of the body, such as the lung, breast, or skin. These tumors can cause vision loss, eye pain, or floaters, and may require treatment with radiation therapy, chemotherapy, or surgery.

It is important to note that retinal neoplasms are relatively rare, and any symptoms or changes in vision should be evaluated by an ophthalmologist as soon as possible to rule out other potential causes and develop an appropriate treatment plan.

Lymphoma is a type of cancer that originates from the white blood cells called lymphocytes, which are part of the immune system. These cells are found in various parts of the body such as the lymph nodes, spleen, bone marrow, and other organs. Lymphoma can be classified into two main types: Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL).

HL is characterized by the presence of a specific type of abnormal lymphocyte called Reed-Sternberg cells, while NHL includes a diverse group of lymphomas that lack these cells. The symptoms of lymphoma may include swollen lymph nodes, fever, night sweats, weight loss, and fatigue.

The exact cause of lymphoma is not known, but it is believed to result from genetic mutations in the lymphocytes that lead to uncontrolled cell growth and division. Exposure to certain viruses, chemicals, and radiation may increase the risk of developing lymphoma. Treatment options for lymphoma depend on various factors such as the type and stage of the disease, age, and overall health of the patient. Common treatments include chemotherapy, radiation therapy, immunotherapy, and stem cell transplantation.

The vitreous body, also known simply as the vitreous, is the clear, gel-like substance that fills the space between the lens and the retina in the eye. It is composed mainly of water, but also contains collagen fibers, hyaluronic acid, and other proteins. The vitreous helps to maintain the shape of the eye and provides a transparent medium for light to pass through to reach the retina. With age, the vitreous can become more liquefied and may eventually separate from the retina, leading to symptoms such as floaters or flashes of light.

B-cell lymphoma is a type of cancer that originates from the B-lymphocytes, which are a part of the immune system and play a crucial role in fighting infections. These cells can develop mutations in their DNA, leading to uncontrolled growth and division, resulting in the formation of a tumor.

B-cell lymphomas can be classified into two main categories: Hodgkin's lymphoma and non-Hodgkin's lymphoma. B-cell lymphomas are further divided into subtypes based on their specific characteristics, such as the appearance of the cells under a microscope, the genetic changes present in the cancer cells, and the aggressiveness of the disease.

Some common types of B-cell lymphomas include diffuse large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, and Burkitt lymphoma. Treatment options for B-cell lymphomas depend on the specific subtype, stage of the disease, and other individual factors. Treatment may include chemotherapy, radiation therapy, immunotherapy, targeted therapy, or stem cell transplantation.

A vitrectomy is a surgical procedure that involves the removal of some or all of the vitreous humor, which is the clear gel-like substance filling the center of the eye. This surgery is often performed to treat various retinal disorders such as diabetic retinopathy, retinal detachment, macular hole, and vitreous hemorrhage.

During a vitrectomy, the ophthalmologist makes small incisions in the sclera (the white part of the eye) to access the vitreous cavity. The surgeon then uses specialized instruments to remove the cloudy or damaged vitreous and may also repair any damage to the retina or surrounding tissues. Afterward, a clear saline solution is injected into the eye to maintain its shape and help facilitate healing.

In some cases, a gas bubble or silicone oil may be placed in the eye after the vitrectomy to help hold the retina in place while it heals. These substances will gradually be absorbed or removed during follow-up appointments. The body naturally produces a new, clear vitreous to replace the removed material over time.

Vitrectomy is typically performed under local anesthesia and may require hospitalization or outpatient care depending on the individual case. Potential risks and complications include infection, bleeding, cataract formation, retinal detachment, and increased eye pressure. However, with proper care and follow-up, most patients experience improved vision after a successful vitrectomy procedure.

Large B-cell lymphoma, diffuse is a type of cancer that starts in cells called B-lymphocytes, which are part of the body's immune system. "Large B-cell" refers to the size and appearance of the abnormal cells when viewed under a microscope. "Diffuse" means that the abnormal cells are spread throughout the lymph node or tissue where the cancer has started, rather than being clustered in one area.

This type of lymphoma is typically aggressive, which means it grows and spreads quickly. It can occur almost anywhere in the body, but most commonly affects the lymph nodes, spleen, and bone marrow. Symptoms may include swollen lymph nodes, fever, night sweats, weight loss, and fatigue.

Treatment for large B-cell lymphoma, diffuse typically involves chemotherapy, radiation therapy, or a combination of both. In some cases, stem cell transplantation or targeted therapy may also be recommended. The prognosis varies depending on several factors, including the stage and location of the cancer, as well as the patient's age and overall health.

Intraocular pressure (IOP) is the fluid pressure within the eye, specifically within the anterior chamber, which is the space between the cornea and the iris. It is measured in millimeters of mercury (mmHg). The aqueous humor, a clear fluid that fills the anterior chamber, is constantly produced and drained, maintaining a balance that determines the IOP. Normal IOP ranges from 10-21 mmHg, with average values around 15-16 mmHg. Elevated IOP is a key risk factor for glaucoma, a group of eye conditions that can lead to optic nerve damage and vision loss if not treated promptly and effectively. Regular monitoring of IOP is essential in diagnosing and managing glaucoma and other ocular health issues.

Non-Hodgkin lymphoma (NHL) is a type of cancer that originates in the lymphatic system, which is part of the immune system. It involves the abnormal growth and proliferation of malignant lymphocytes (a type of white blood cell), leading to the formation of tumors in lymph nodes, spleen, bone marrow, or other organs. NHL can be further classified into various subtypes based on the specific type of lymphocyte involved and its characteristics.

The symptoms of Non-Hodgkin lymphoma may include:

* Painless swelling of lymph nodes in the neck, armpits, or groin
* Persistent fatigue
* Unexplained weight loss
* Fever
* Night sweats
* Itchy skin

The exact cause of Non-Hodgkin lymphoma is not well understood, but it has been associated with certain risk factors such as age (most common in people over 60), exposure to certain chemicals, immune system deficiencies, and infection with viruses like Epstein-Barr virus or HIV.

Treatment for Non-Hodgkin lymphoma depends on the stage and subtype of the disease, as well as the patient's overall health. Treatment options may include chemotherapy, radiation therapy, immunotherapy, targeted therapy, stem cell transplantation, or a combination of these approaches. Regular follow-up care is essential to monitor the progression of the disease and manage any potential long-term side effects of treatment.

Central nervous system (CNS) neoplasms refer to a group of abnormal growths or tumors that develop within the brain or spinal cord. These tumors can be benign or malignant, and their growth can compress or disrupt the normal functioning of surrounding brain or spinal cord tissue.

Benign CNS neoplasms are slow-growing and rarely spread to other parts of the body. However, they can still cause significant problems if they grow large enough to put pressure on vital structures within the brain or spinal cord. Malignant CNS neoplasms, on the other hand, are aggressive tumors that can invade and destroy surrounding tissue. They may also spread to other parts of the CNS or, rarely, to other organs in the body.

CNS neoplasms can arise from various types of cells within the brain or spinal cord, including nerve cells, glial cells (which provide support and insulation for nerve cells), and supportive tissues such as blood vessels. The specific type of CNS neoplasm is often used to help guide treatment decisions and determine prognosis.

Symptoms of CNS neoplasms can vary widely depending on the location and size of the tumor, but may include headaches, seizures, weakness or paralysis, vision or hearing changes, balance problems, memory loss, and changes in behavior or personality. Treatment options for CNS neoplasms may include surgery, radiation therapy, chemotherapy, or a combination of these approaches.

Uveitis is the inflammation of the uvea, the middle layer of the eye between the retina and the white of the eye (sclera). The uvea consists of the iris, ciliary body, and choroid. Uveitis can cause redness, pain, and vision loss. It can be caused by various systemic diseases, infections, or trauma. Depending on the part of the uvea that's affected, uveitis can be classified as anterior (iritis), intermediate (cyclitis), posterior (choroiditis), or pan-uveitis (affecting all layers). Treatment typically includes corticosteroids and other immunosuppressive drugs to control inflammation.

Intraocular lenses (IOLs) are artificial lens implants that are placed inside the eye during ophthalmic surgery, such as cataract removal. These lenses are designed to replace the natural lens of the eye that has become clouded or damaged, thereby restoring vision impairment caused by cataracts or other conditions.

There are several types of intraocular lenses available, including monofocal, multifocal, toric, and accommodative lenses. Monofocal IOLs provide clear vision at a single fixed distance, while multifocal IOLs offer clear vision at multiple distances. Toric IOLs are designed to correct astigmatism, and accommodative IOLs can change shape and position within the eye to allow for a range of vision.

The selection of the appropriate type of intraocular lens depends on various factors, including the patient's individual visual needs, lifestyle, and ocular health. The implantation procedure is typically performed on an outpatient basis and involves minimal discomfort or recovery time. Overall, intraocular lenses have become a safe and effective treatment option for patients with vision impairment due to cataracts or other eye conditions.

T-cell lymphoma is a type of cancer that affects the T-cells, which are a specific type of white blood cell responsible for immune function. These lymphomas develop from mature T-cells and can be classified into various subtypes based on their clinical and pathological features.

T-cell lymphomas can arise in many different organs, including the lymph nodes, skin, and other soft tissues. They often present with symptoms such as enlarged lymph nodes, fever, night sweats, and weight loss. The diagnosis of T-cell lymphoma typically involves a biopsy of the affected tissue, followed by immunophenotyping and genetic analysis to determine the specific subtype.

Treatment for T-cell lymphomas may include chemotherapy, radiation therapy, immunotherapy, or stem cell transplantation, depending on the stage and aggressiveness of the disease. The prognosis for T-cell lymphoma varies widely depending on the subtype and individual patient factors.

Intraocular lens (IOL) implantation is a surgical procedure that involves placing a small artificial lens inside the eye to replace the natural lens that has been removed. This procedure is typically performed during cataract surgery, where the cloudy natural lens is removed and replaced with an IOL to restore clear vision.

During the procedure, a small incision is made in the eye, and the cloudy lens is broken up and removed using ultrasound waves or laser energy. Then, the folded IOL is inserted through the same incision and positioned in the correct place inside the eye. Once in place, the IOL unfolds and is secured into position.

There are several types of IOLs available, including monofocal, multifocal, toric, and accommodating lenses. Monofocal lenses provide clear vision at one distance, while multifocal lenses offer clear vision at multiple distances. Toric lenses correct astigmatism, and accommodating lenses can change shape to focus on objects at different distances.

Overall, intraocular lens implantation is a safe and effective procedure that can help restore clear vision in patients with cataracts or other eye conditions that require the removal of the natural lens.

Follicular lymphoma is a specific type of low-grade or indolent non-Hodgkin lymphoma (NHL). It develops from the B-lymphocytes, a type of white blood cell found in the lymphatic system. This lymphoma is characterized by the presence of abnormal follicles or nodules in the lymph nodes and other organs. The neoplastic cells in this subtype exhibit a distinct growth pattern that resembles normal follicular centers, hence the name "follicular lymphoma."

The majority of cases involve a translocation between chromosomes 14 and 18 [t(14;18)], leading to an overexpression of the BCL-2 gene. This genetic alteration contributes to the cancer cells' resistance to programmed cell death, allowing them to accumulate in the body.

Follicular lymphoma is typically slow-growing and may not cause symptoms for a long time. Common manifestations include painless swelling of lymph nodes, fatigue, weight loss, and night sweats. Treatment options depend on various factors such as the stage of the disease, patient's age, and overall health. Watchful waiting, chemotherapy, immunotherapy, targeted therapy, radiation therapy, or a combination of these approaches may be used to manage follicular lymphoma.

Burkitt lymphoma is a type of aggressive non-Hodgkin lymphoma (NHL), which is a cancer that originates in the lymphatic system. It is named after Denis Parsons Burkitt, an Irish surgeon who first described this form of cancer in African children in the 1950s.

Burkitt lymphoma is characterized by the rapid growth and spread of abnormal B-lymphocytes (a type of white blood cell), which can affect various organs and tissues, including the lymph nodes, spleen, liver, gastrointestinal tract, and central nervous system.

There are three main types of Burkitt lymphoma: endemic, sporadic, and immunodeficiency-associated. The endemic form is most common in equatorial Africa and is strongly associated with Epstein-Barr virus (EBV) infection. The sporadic form occurs worldwide but is rare, accounting for less than 1% of all NHL cases in the United States. Immunodeficiency-associated Burkitt lymphoma is seen in individuals with weakened immune systems due to HIV/AIDS or immunosuppressive therapy after organ transplantation.

Burkitt lymphoma typically presents as a rapidly growing mass, often involving the jaw, facial bones, or abdominal organs. Symptoms may include swollen lymph nodes, fever, night sweats, weight loss, and fatigue. Diagnosis is made through a biopsy of the affected tissue, followed by immunohistochemical staining and genetic analysis to confirm the presence of characteristic chromosomal translocations involving the MYC oncogene.

Treatment for Burkitt lymphoma typically involves intensive chemotherapy regimens, often combined with targeted therapy or immunotherapy. The prognosis is generally good when treated aggressively and promptly, with a high cure rate in children and young adults. However, the prognosis may be poorer in older patients or those with advanced-stage disease at diagnosis.

B-cell marginal zone lymphoma (MZL) is a type of indolent (slow-growing) non-Hodgkin lymphoma (NHL). It arises from B-lymphocytes, a type of white blood cell found in the lymphatic system. MZLs typically involve the marginal zone of lymphoid follicles, which are structures found in lymph nodes and other lymphatic tissues.

There are three subtypes of MZL: extranodal MZL (also known as mucosa-associated lymphoid tissue or MALT lymphoma), nodal MZL, and splenic MZL. Extranodal MZL is the most common form and can occur at various extranodal sites, such as the stomach, lungs, skin, eyes, and salivary glands. Nodal MZL involves the lymph nodes without evidence of extranodal disease, while splenic MZL primarily affects the spleen.

MZLs are typically low-grade malignancies, but they can transform into more aggressive forms over time. Treatment options depend on the stage and location of the disease, as well as the patient's overall health. Common treatments include watchful waiting, radiation therapy, chemotherapy, immunotherapy, targeted therapy, or a combination of these approaches.

Ocular tonometry is a medical test used to measure the pressure inside the eye, also known as intraocular pressure (IOP). This test is an essential part of diagnosing and monitoring glaucoma, a group of eye conditions that can cause vision loss and blindness due to damage to the optic nerve from high IOP.

The most common method of ocular tonometry involves using a tonometer device that gently touches the front surface of the eye (cornea) with a small probe or prism. The device measures the amount of force required to flatten the cornea slightly, which correlates with the pressure inside the eye. Other methods of ocular tonometry include applanation tonometry, which uses a small amount of fluorescein dye and a blue light to measure the IOP, and rebound tonometry, which uses a lightweight probe that briefly touches the cornea and then bounces back to determine the IOP.

Regular ocular tonometry is important for detecting glaucoma early and preventing vision loss. It is typically performed during routine eye exams and may be recommended more frequently for individuals at higher risk of developing glaucoma, such as those with a family history of the condition or certain medical conditions like diabetes.

Mantle cell lymphoma (MCL) is a type of non-Hodgkin lymphoma (NHL), which is a cancer of the lymphatic system. Specifically, MCL arises from abnormal B-lymphocytes (a type of white blood cell) that typically reside in the "mantle zone" of the lymph node. The malignant cells in MCL tend to have a characteristic genetic abnormality where the cyclin D1 gene is translocated to the immunoglobulin heavy chain gene locus, resulting in overexpression of cyclin D1 protein. This leads to uncontrolled cell division and proliferation.

Mantle cell lymphoma often presents with advanced-stage disease, involving multiple lymph nodes, bone marrow, and sometimes extranodal sites such as the gastrointestinal tract. Symptoms may include swollen lymph nodes, fatigue, weight loss, night sweats, and abdominal pain or discomfort.

Treatment for MCL typically involves a combination of chemotherapy, immunotherapy, and sometimes targeted therapy or stem cell transplantation. However, the prognosis for MCL is generally less favorable compared to other types of NHL, with a median overall survival of around 5-7 years.

Glaucoma is a group of eye conditions that damage the optic nerve, often caused by an abnormally high pressure in the eye (intraocular pressure). This damage can lead to permanent vision loss or even blindness if left untreated. The most common type is open-angle glaucoma, which has no warning signs and progresses slowly. Angle-closure glaucoma, on the other hand, can cause sudden eye pain, redness, nausea, and vomiting, as well as rapid vision loss. Other less common types of glaucoma also exist. While there is no cure for glaucoma, early detection and treatment can help slow or prevent further vision loss.

Cutaneous T-cell lymphoma (CTCL) is a type of cancer that affects T-cells, a specific group of white blood cells called lymphocytes. These cells play a crucial role in the body's immune system and help protect against infection and disease. In CTCL, the T-cells become malignant and accumulate in the skin, leading to various skin symptoms and lesions.

CTCL is a subtype of non-Hodgkin lymphoma (NHL), which refers to a group of cancers that originate from lymphocytes. Within NHL, CTCL is categorized as a type of extranodal lymphoma since it primarily involves organs or tissues outside the lymphatic system, in this case, the skin.

The two most common subtypes of CTCL are mycosis fungoides and Sézary syndrome:

1. Mycosis fungoides (MF): This is the more prevalent form of CTCL, characterized by patches, plaques, or tumors on the skin. The lesions may be scaly, itchy, or change in size, shape, and color over time. MF usually progresses slowly, with early-stage disease often confined to the skin for several years before spreading to lymph nodes or other organs.
2. Sézary syndrome (SS): This is a more aggressive form of CTCL that involves not only the skin but also the blood and lymph nodes. SS is characterized by the presence of malignant T-cells, known as Sézary cells, in the peripheral blood. Patients with SS typically have generalized erythroderma (reddening and scaling of the entire body), pruritus (severe itching), lymphadenopathy (swollen lymph nodes), and alopecia (hair loss).

The diagnosis of CTCL usually involves a combination of clinical examination, skin biopsy, and immunophenotyping to identify the malignant T-cells. Treatment options depend on the stage and subtype of the disease and may include topical therapies, phototherapy, systemic medications, or targeted therapies.

Ocular hypertension is a medical condition characterized by elevated pressure within the eye (intraocular pressure or IOP), which is higher than normal but not necessarily high enough to cause any visible damage to the optic nerve or visual field loss. It serves as a significant risk factor for developing glaucoma, a sight-threatening disease.

The normal range of intraocular pressure is typically between 10-21 mmHg (millimeters of mercury). Ocular hypertension is often defined as an IOP consistently above 21 mmHg, although some studies suggest that even pressures between 22-30 mmHg may not cause damage in all individuals. Regular monitoring and follow-up with an ophthalmologist are essential for people diagnosed with ocular hypertension to ensure early detection and management of any potential glaucomatous changes. Treatment options include medications, laser therapy, or surgery to lower the IOP and reduce the risk of glaucoma onset.

Aqueous humor is a clear, watery fluid that fills the anterior and posterior chambers of the eye. It is produced by the ciliary processes in the posterior chamber and circulates through the pupil into the anterior chamber, where it provides nutrients to the cornea and lens, maintains intraocular pressure, and helps to shape the eye. The aqueous humor then drains out of the eye through the trabecular meshwork and into the canal of Schlemm, eventually reaching the venous system.

T-cell peripheral lymphoma is a type of cancer that affects the T-cells, which are a type of white blood cell that plays a crucial role in the body's immune system. This type of lymphoma is called "peripheral" because it typically develops in T-cells that have matured and are found in various tissues and organs outside of the bone marrow, such as the lymph nodes, spleen, skin, and digestive tract.

Peripheral T-cell lymphomas (PTCL) are relatively rare and can be aggressive, with a tendency to spread quickly throughout the body. They can arise from different types of T-cells, leading to various subtypes of PTCL that may have different clinical features, treatment options, and prognoses.

Some common subtypes of peripheral T-cell lymphoma include:

1. PTCL, not otherwise specified (NOS): This is the most common subtype, accounting for about 25-30% of all PTCL cases. It includes cases that do not fit into any specific category or have features of more than one subtype.
2. Anaplastic large cell lymphoma (ALCL): ALCL can be further divided into two groups: systemic ALCL and cutaneous ALCL. Systemic ALCL is a more aggressive form, while cutaneous ALCL tends to be less aggressive and primarily affects the skin.
3. Angioimmunoblastic T-cell lymphoma (AITL): AITL is an aggressive subtype that often involves the lymph nodes and can affect other organs such as the spleen, liver, and bone marrow. It frequently presents with B symptoms (fever, night sweats, and weight loss) and abnormal blood tests.
4. Enteropathy-associated T-cell lymphoma (EATL): EATL is a rare but aggressive subtype that primarily affects the intestines, particularly in individuals with a history of celiac disease or gluten sensitivity.
5. Adult T-cell leukemia/lymphoma (ATLL): ATLL is caused by the human T-cell leukemia virus type 1 (HTLV-1) and primarily affects adults from regions where HTLV-1 is endemic, such as Japan, the Caribbean, and parts of Africa.

Treatment for PTCL depends on the specific subtype, stage, and individual patient factors. Common treatment options include chemotherapy, targeted therapy, immunotherapy, radiation therapy, stem cell transplantation, or a combination of these approaches. Clinical trials are also available for eligible patients to test new therapies and combinations.

AIDS-related lymphoma (ARL) is a type of cancer that affects the lymphatic system and is associated with acquired immunodeficiency syndrome (AIDS). It is caused by the infection of the lymphocytes, a type of white blood cell, with the human immunodeficiency virus (HIV), which weakens the immune system and makes individuals more susceptible to developing lymphoma.

There are two main types of AIDS-related lymphomas: diffuse large B-cell lymphoma (DLBCL) and Burkitt lymphoma (BL). DLBCL is the most common type and tends to grow rapidly, while BL is a more aggressive form that can also spread quickly.

Symptoms of AIDS-related lymphoma may include swollen lymph nodes, fever, night sweats, fatigue, weight loss, and decreased appetite. Diagnosis typically involves a biopsy of the affected lymph node or other tissue, followed by various imaging tests to determine the extent of the disease.

Treatment for AIDS-related lymphoma usually involves a combination of chemotherapy, radiation therapy, and/or immunotherapy, along with antiretroviral therapy (ART) to manage HIV infection. The prognosis for ARL varies depending on several factors, including the type and stage of the disease, the patient's overall health, and their response to treatment.

Large cell anaplastic lymphoma is a type of cancer that starts in white blood cells called lymphocytes, which are part of the body's immune system. It is classified as a type of non-Hodgkin lymphoma (NHL).

Anaplastic large cell lymphoma (ALCL) is a subtype of NHL characterized by the presence of large cancer cells that look abnormal under a microscope. These cells are called "anaplastic" because they lack many of the usual features of mature lymphocytes.

ALCL can occur in many different parts of the body, including the lymph nodes, skin, lungs, and soft tissues. It is typically an aggressive form of NHL that grows and spreads quickly.

ALCL is further divided into two main subtypes based on the presence or absence of a genetic abnormality involving a protein called ALK (anaplastic lymphoma kinase). ALK-positive ALCL tends to occur in younger patients and has a better prognosis than ALK-negative ALCL.

Treatment for large cell anaplastic lymphoma typically involves chemotherapy, radiation therapy, and/or immunotherapy, depending on the stage and location of the cancer. In some cases, stem cell transplantation may also be recommended.

Phacoemulsification is a surgical procedure used in cataract removal. It involves using an ultrasonic device to emulsify (break up) the cloudy lens (cataract) into small pieces, which are then aspirated or sucked out through a small incision. This procedure allows for smaller incisions and faster recovery times compared to traditional cataract surgery methods. After the cataract is removed, an artificial intraocular lens (IOL) is typically implanted to replace the natural lens and restore vision.

Cataract extraction is a surgical procedure that involves removing the cloudy lens (cataract) from the eye. This procedure is typically performed to restore vision impairment caused by cataracts and improve overall quality of life. There are two primary methods for cataract extraction:

1. Phacoemulsification: This is the most common method used today. It involves making a small incision in the front part of the eye (cornea), inserting an ultrasonic probe to break up the cloudy lens into tiny pieces, and then removing those pieces with suction. After removing the cataract, an artificial intraocular lens (IOL) is inserted to replace the natural lens and help focus light onto the retina.

2. Extracapsular Cataract Extraction: In this method, a larger incision is made on the side of the cornea, allowing the surgeon to remove the cloudy lens in one piece without breaking it up. The back part of the lens capsule is left intact to support the IOL. This technique is less common and typically reserved for more advanced cataracts or when phacoemulsification cannot be performed.

Recovery from cataract extraction usually involves using eye drops to prevent infection and inflammation, as well as protecting the eye with a shield or glasses during sleep for a few weeks after surgery. Most people experience improved vision within a few days to a week following the procedure.

The anterior chamber is the front portion of the eye, located between the cornea (the clear front "window" of the eye) and the iris (the colored part of the eye). It is filled with a clear fluid called aqueous humor that provides nutrients to the structures inside the eye and helps maintain its shape. The anterior chamber plays an important role in maintaining the overall health and function of the eye.

Open-angle glaucoma is a chronic, progressive type of glaucoma characterized by the gradual loss of optic nerve fibers and resulting in visual field defects. It is called "open-angle" because the angle where the iris meets the cornea (trabecular meshwork) appears to be normal and open on examination. The exact cause of this condition is not fully understood, but it is associated with increased resistance to the outflow of aqueous humor within the trabecular meshwork, leading to an increase in intraocular pressure (IOP). This elevated IOP can cause damage to the optic nerve and result in vision loss.

The onset of open-angle glaucoma is often asymptomatic, making regular comprehensive eye examinations crucial for early detection and management. Treatment typically involves lowering IOP using medications, laser therapy, or surgery to prevent further optic nerve damage and preserve vision.

Hodgkin disease, also known as Hodgkin lymphoma, is a type of cancer that originates in the white blood cells called lymphocytes. It typically affects the lymphatic system, which is a network of vessels and glands spread throughout the body. The disease is characterized by the presence of a specific type of abnormal cell, known as a Reed-Sternberg cell, within the affected lymph nodes.

The symptoms of Hodgkin disease may include painless swelling of the lymph nodes in the neck, armpits, or groin; fever; night sweats; weight loss; and fatigue. The exact cause of Hodgkin disease is unknown, but it is thought to involve a combination of genetic, environmental, and infectious factors.

Hodgkin disease is typically treated with a combination of chemotherapy, radiation therapy, and/or immunotherapy, depending on the stage and extent of the disease. With appropriate treatment, the prognosis for Hodgkin disease is generally very good, with a high cure rate. However, long-term side effects of treatment may include an increased risk of secondary cancers and other health problems.

Foreign bodies in the eye refer to any object or particle that is not normally present in the eye and becomes lodged in it. These foreign bodies can range from small particles like sand or dust to larger objects such as metal shavings or glass. They can cause irritation, pain, redness, watering, and even vision loss if they are not removed promptly and properly.

The symptoms of an eye foreign body may include:

* A feeling that something is in the eye
* Pain or discomfort in the eye
* Redness or inflammation of the eye
* Watering or tearing of the eye
* Sensitivity to light
* Blurred vision or difficulty seeing

If you suspect that you have a foreign body in your eye, it is important to seek medical attention immediately. An eye care professional can examine your eye and determine the best course of treatment to remove the foreign body and prevent any further damage to your eye.

The eye is the organ of sight, primarily responsible for detecting and focusing on visual stimuli. It is a complex structure composed of various parts that work together to enable vision. Here are some of the main components of the eye:

1. Cornea: The clear front part of the eye that refracts light entering the eye and protects the eye from harmful particles and microorganisms.
2. Iris: The colored part of the eye that controls the amount of light reaching the retina by adjusting the size of the pupil.
3. Pupil: The opening in the center of the iris that allows light to enter the eye.
4. Lens: A biconvex structure located behind the iris that further refracts light and focuses it onto the retina.
5. Retina: A layer of light-sensitive cells (rods and cones) at the back of the eye that convert light into electrical signals, which are then transmitted to the brain via the optic nerve.
6. Optic Nerve: The nerve that carries visual information from the retina to the brain.
7. Vitreous: A clear, gel-like substance that fills the space between the lens and the retina, providing structural support to the eye.
8. Conjunctiva: A thin, transparent membrane that covers the front of the eye and the inner surface of the eyelids.
9. Extraocular Muscles: Six muscles that control the movement of the eye, allowing for proper alignment and focus.

The eye is a remarkable organ that allows us to perceive and interact with our surroundings. Various medical specialties, such as ophthalmology and optometry, are dedicated to the diagnosis, treatment, and management of various eye conditions and diseases.

Visual acuity is a measure of the sharpness or clarity of vision. It is usually tested by reading an eye chart from a specific distance, such as 20 feet (6 meters). The standard eye chart used for this purpose is called the Snellen chart, which contains rows of letters that decrease in size as you read down the chart.

Visual acuity is typically expressed as a fraction, with the numerator representing the testing distance and the denominator indicating the smallest line of type that can be read clearly. For example, if a person can read the line on the eye chart that corresponds to a visual acuity of 20/20, it means they have normal vision at 20 feet. If their visual acuity is 20/40, it means they must be as close as 20 feet to see what someone with normal vision can see at 40 feet.

It's important to note that visual acuity is just one aspect of overall vision and does not necessarily reflect other important factors such as peripheral vision, depth perception, color vision, or contrast sensitivity.

Timolol is a non-selective beta blocker drug that is primarily used to treat hypertension, angina pectoris, and glaucoma. It works by blocking the action of certain hormones such as epinephrine (adrenaline) on the heart and blood vessels, which helps to lower heart rate, reduce the force of heart muscle contraction, and decrease blood vessel constriction. These effects can help to lower blood pressure, reduce the workload on the heart, and improve oxygen supply to the heart muscle. In glaucoma treatment, timolol reduces the production of aqueous humor in the eye, thereby decreasing intraocular pressure.

The medical definition of Timolol is:

Timolol (tim-oh-lol) is a beta-adrenergic receptor antagonist used to treat hypertension, angina pectoris, and glaucoma. It works by blocking the action of epinephrine on the heart and blood vessels, which results in decreased heart rate, reduced force of heart muscle contraction, and decreased blood vessel constriction. In glaucoma treatment, timolol reduces aqueous humor production, thereby decreasing intraocular pressure. Timolol is available as an oral tablet, solution for injection, and ophthalmic solution.

Endophthalmitis is a serious inflammatory eye condition that occurs when an infection develops inside the eyeball, specifically within the vitreous humor (the clear, gel-like substance that fills the space between the lens and the retina). This condition can be caused by bacteria, fungi, or other microorganisms that enter the eye through various means, such as trauma, surgery, or spread from another infected part of the body.

Endophthalmitis is often characterized by symptoms like sudden onset of pain, redness, decreased vision, and increased sensitivity to light (photophobia). If left untreated, it can lead to severe complications, including blindness. Treatment typically involves administering antibiotics or antifungal medications, either systemically or directly into the eye, and sometimes even requiring surgical intervention to remove infected tissues and relieve intraocular pressure.

The sclera is the tough, white, fibrous outer coating of the eye in humans and other vertebrates, covering about five sixths of the eyeball's surface. It provides protection for the delicate inner structures of the eye and maintains its shape. The sclera is composed mainly of collagen and elastic fiber, making it strong and resilient. Its name comes from the Greek word "skleros," which means hard.

Intraocular injections are a type of medical procedure where medication is administered directly into the eye. This technique is often used to deliver drugs that treat various eye conditions, such as age-related macular degeneration, diabetic retinopathy, and endophthalmitis. The most common type of intraocular injection is an intravitreal injection, which involves injecting medication into the vitreous cavity, the space inside the eye filled with a clear gel-like substance called the vitreous humor. This procedure is typically performed by an ophthalmologist in a clinical setting and may be repeated at regular intervals depending on the condition being treated.

Ophthalmic solutions are sterile, single-use or multi-dose preparations in a liquid form that are intended for topical administration to the eye. These solutions can contain various types of medications, such as antibiotics, anti-inflammatory agents, antihistamines, or lubricants, which are used to treat or prevent ocular diseases and conditions.

The pH and osmolarity of ophthalmic solutions are carefully controlled to match the physiological environment of the eye and minimize any potential discomfort or irritation. The solutions may be packaged in various forms, including drops, sprays, or irrigations, depending on the intended use and administration route.

It is important to follow the instructions for use provided by a healthcare professional when administering ophthalmic solutions, as improper use can lead to eye injury or reduced effectiveness of the medication.

The ciliary body is a part of the eye's internal structure that is located between the choroid and the iris. It is composed of muscle tissue and is responsible for adjusting the shape of the lens through a process called accommodation, which allows the eye to focus on objects at varying distances. Additionally, the ciliary body produces aqueous humor, the clear fluid that fills the anterior chamber of the eye and helps to nourish the eye's internal structures. The ciliary body is also responsible for maintaining the shape and position of the lens within the eye.

Large B-cell lymphoma, immunoblastic variant, is a type of cancer that starts in the white blood cells called lymphocytes, which are part of the body's immune system. It is a subtype of diffuse large B-cell lymphoma (DLBCL), which is an aggressive (fast-growing) lymphoma.

Immunoblastic large B-cell lymphoma is characterized by the presence of large, immunoblastic cells that have a specific appearance under the microscope. These cells are typically found in the lymph nodes or other lymphoid tissues, such as the spleen or bone marrow.

This type of lymphoma can be aggressive and may require prompt treatment with chemotherapy, radiation therapy, or stem cell transplantation. The prognosis for immunoblastic large B-cell lymphoma varies depending on several factors, including the stage of the disease at diagnosis, the patient's age and overall health, and the specific features of the tumor.

It is important to note that a medical definition may vary based on different medical sources or guidelines, and it is always best to consult with a healthcare professional for accurate information.

A trabeculectomy is a surgical procedure performed on the eye to treat glaucoma, an eye condition characterized by increased pressure within the eye that can lead to optic nerve damage and vision loss. The main goal of this operation is to create a new channel for the aqueous humor (the clear fluid inside the eye) to drain out, thus reducing the intraocular pressure (IOP).

During the trabeculectomy procedure, a small flap is made in the sclera (the white part of the eye), and a piece of the trabecular meshwork (a structure inside the eye that helps regulate the flow of aqueous humor) is removed. This opening allows the aqueous humor to bypass the obstructed drainage system and form a bleb, a small blister-like sac on the surface of the eye, which absorbs the fluid and reduces IOP.

The success of trabeculectomy depends on various factors, including the patient's age, type and severity of glaucoma, previous treatments, and overall health. Potential complications may include infection, bleeding, cataract formation, hypotony (abnormally low IOP), or failure to control IOP. Regular follow-up appointments with an ophthalmologist are necessary to monitor the eye's response to the surgery and manage any potential issues that may arise.

In medical terms, the iris refers to the colored portion of the eye that surrounds the pupil. It is a circular structure composed of thin, contractile muscle fibers (radial and circumferential) arranged in a regular pattern. These muscles are controlled by the autonomic nervous system and can adjust the size of the pupil in response to changes in light intensity or emotional arousal. By constricting or dilating the iris, the amount of light entering the eye can be regulated, which helps maintain optimal visual acuity under various lighting conditions.

The color of the iris is determined by the concentration and distribution of melanin pigments within the iris stroma. The iris also contains blood vessels, nerves, and connective tissue that support its structure and function. Anatomically, the iris is continuous with the ciliary body and the choroid, forming part of the uveal tract in the eye.

Phakic Intraocular Lenses (PIOLs) are a type of surgical implant used in refractive eye surgery to correct vision problems such as myopia (nearsightedness), hyperopia (farsightedness), and astigmatism. These lenses are placed inside the eye, specifically between the cornea and the natural lens (crystalline lens) of the eye, without removing the natural lens. This is why they are called "phakic," which means the natural lens remains in place.

PIOLs can provide an alternative to other refractive surgeries like LASIK or PRK, particularly for individuals with high levels of refractive error who may not be suitable candidates for those procedures. The procedure to implant a phakic intraocular lens is typically performed on an outpatient basis and takes only a few minutes.

There are two main types of PIOLs: anterior chamber phakic lenses, which are placed in front of the iris, and posterior chamber phakic lenses, which are placed behind the iris but in front of the natural lens. Both types of lenses have their own advantages and disadvantages, and the choice between them depends on various factors such as the patient's eye anatomy and the specific type and degree of refractive error.

It is important to note that, like any surgical procedure, there are potential risks associated with PIOL implantation, including infection, increased intraocular pressure, cataract formation, and changes in vision. Therefore, a thorough evaluation by an eye care professional is necessary before deciding if this type of surgery is appropriate for an individual patient.

The trabecular meshwork is a specialized tissue located in the anterior chamber angle of the eye, near the iris and cornea. It is composed of a network of interconnected beams or trabeculae that provide support and structure to the eye. The primary function of the trabecular meshwork is to regulate the outflow of aqueous humor, the fluid that fills the anterior chamber of the eye, and maintain intraocular pressure within normal ranges.

The aqueous humor flows from the ciliary processes in the posterior chamber of the eye through the pupil and into the anterior chamber. From there, it drains out of the eye through the trabecular meshwork and into the canal of Schlemm, which leads to the venous system. Any obstruction or damage to the trabecular meshwork can lead to an increase in intraocular pressure and potentially contribute to the development of glaucoma, a leading cause of irreversible blindness worldwide.

Pseudophakia is a medical term that refers to the condition where a person's natural lens in the eye has been replaced with an artificial one. This procedure is typically performed during cataract surgery, where the cloudy, natural lens is removed and replaced with a clear, artificial lens to improve vision. The prefix "pseudo" means false or fake, and "phakia" refers to the natural lens of the eye, hence the term "Pseudophakia" implies a false or artificial lens.

Ocular hypotension is a medical term that refers to a condition where the pressure inside the eye (intraocular pressure or IOP) is lower than normal. The normal range for IOP is typically between 10-21 mmHg (millimeters of mercury). Ocular hypotension can occur due to various reasons, including certain medications, medical conditions, or surgical procedures that affect the eye's ability to produce or drain aqueous humor, the clear fluid inside the eye.

While mild ocular hypotension may not cause any symptoms, more significant cases can lead to complications such as decreased vision, optic nerve damage, and visual field loss. If left untreated, it could potentially result in a condition called glaucoma. It is essential to consult an eye care professional if you suspect ocular hypotension or experience any changes in your vision.

Vincristine is an antineoplastic agent, specifically a vinca alkaloid. It is derived from the Madagascar periwinkle plant (Catharanthus roseus). Vincristine binds to tubulin, a protein found in microtubules, and inhibits their polymerization, which results in disruption of mitotic spindles leading to cell cycle arrest and apoptosis (programmed cell death). It is used in the treatment of various types of cancer including leukemias, lymphomas, and solid tumors. Common side effects include peripheral neuropathy, constipation, and alopecia.

Prostaglandins F (PGF) are a type of prostaglandin, which are naturally occurring hormone-like substances that have various effects on the body. They are produced in response to injury or infection and play a role in inflammation, fever, and pain. Prostaglandins F are synthesized for medical use and are available as drugs known as dinoprost and cloprostenol.

Dinoprost is a synthetic form of PGF2α (prostaglandin F2 alpha) used to induce labor and treat postpartum hemorrhage. It works by causing the uterus to contract, helping to expel the placenta and reduce bleeding.

Cloprostenol is a synthetic form of PGF2α used in veterinary medicine as a reproductive hormone to synchronize estrus cycles in cattle and sheep, as well as to induce parturition (giving birth) in cows. It works by stimulating the contraction of the uterus and promoting the release of luteinizing hormone (LH), which triggers ovulation.

It is important to note that these synthetic prostaglandins should only be used under the supervision of a healthcare professional or veterinarian, as they can have side effects and interactions with other medications.

The anterior eye segment refers to the front portion of the eye, which includes the cornea, iris, ciliary body, and lens. The cornea is the clear, dome-shaped surface at the front of the eye that refracts light entering the eye and provides protection. The iris is the colored part of the eye that controls the amount of light reaching the retina by adjusting the size of the pupil. The ciliary body is a muscle that changes the shape of the lens to focus on objects at different distances. The lens is a transparent structure located behind the iris that further refracts light to provide a clear image. Together, these structures work to focus light onto the retina and enable vision.

A cataract is a clouding of the natural lens in the eye that affects vision. This clouding can cause vision to become blurry, faded, or dim, making it difficult to see clearly. Cataracts are a common age-related condition, but they can also be caused by injury, disease, or medication use. In most cases, cataracts develop gradually over time and can be treated with surgery to remove the cloudy lens and replace it with an artificial one.

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December 2008). "Ifosfamide or trofosfamide in patients with intraocular lymphoma". J. Neurooncol. 93 (2): 213-7. doi:10.1007/ ...
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... in the eyes of patients with primary intraocular lymphoma". Ophthalmology. 110 (2): 421-6. doi:10.1016/S0161-6420(02)01737-2. ... C-X-C chemokine receptor type 5 (CXC-R5) also known as CD185 (cluster of differentiation 185) or Burkitt lymphoma receptor 1 ( ... The BLR1 / CXCR5 gene is specifically expressed in Burkitt's lymphoma and lymphatic tissues, such as follicles in lymph nodes ... "A B-cell-homing chemokine made in lymphoid follicles activates Burkitt's lymphoma receptor-1". Nature. 391 (6669): 799-803. ...
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Valentincic NV, de Groot-Mijnes JD, Kraut A, Korosec P, Hawlina M, Rothova A (2011). "Intraocular and serum cytokine profiles ... retinoblastoma lymphoma malignant melanoma leukemia reticulum cell sarcoma The disease course, anatomy, and laterality can vary ... Non-neoplastic: retinitis pigmentosa intraocular foreign body juvenile xanthogranuloma retinal detachment Neoplastic: ... acute zonal occult outer retinopathy Masquerade syndromes are those conditions that include the presence of intraocular cells ...
Kumar H, Honavar SG, Vajpayee RB (1994). "Nd:YAG laser sweeping of the anterior surface of an intraocular lens: a new ... Mulay K, Narula R, Honavar SG (2015). "Primary vitreoretinal lymphoma". Indian J Ophthalmol. 63 (3): 180-6. doi:10.4103/0301- ... "Lymphoma of the Eyelid - An International Multicenter Retrospective Study". Am J Ophthalmol. 177: 58-68. doi:10.1016/j.ajo. ... "Intraocular cysticercosis simulating retinoblastoma in a 5-year-old child". Eye (Lond). 17 (3): 447-9. doi:10.1038/sj.eye. ...
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Previous studies identified mGRs in lymphoma cells, but it wasn't until 2004 that mGRs were identified in human peripheral ... Ophthalmic: posterior sub-capsular cataracts, increased intraocular pressure, glaucoma, and exophthalmos. Feedback of the ... lymphoma and congenital (erythroid) hypoplastic anemia. Pulmonary: aspiration pneumonitis, chronic beryllium disease, ...
... and some with intraocular infections. Rodents are natural intermediate hosts, and they harbor the cyst-like larvae ( ... "Subcutaneous Taenia crassiceps infection in a patient with non-Hodgkin's lymphoma". Am. J. Trop. Med. Hyg. 75 (1): 108-11. doi: ...
Lymphoma - Cancer of the lymphatic system. Contents: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z See also References ... small portions of the vitreous humor from the front structures of the eye-often because these are tangled in an intraocular ...
Intraocular lymphoma is a rare malignant form of eye cancer. Intraocular lymphoma may affect the eye secondarily from a ... primary intraocular lymphoma, PIOL). PIOL is a subset of primary central nervous system lymphoma (PCNSL). PCNSL (and PIOL) are ... Gonzales, John A.; Chan, Chi-Chao (August 2007). "Biopsy techniques and yields in diagnosing primary intraocular lymphoma". ... "Primary intraocular lymphoma of T-cell type: report of a case and review of the literature". Graefes Archive for Clinical and ...
... known as primary intraocular lymphoma (PIOL), one of the subtypes of lymphoma. ... This entry looks at intraocular lymphoma, known as primary intraocular lymphoma (PIOL), one of the subtypes of lymphoma. ... When a primary lymphoma is found in the eye (an ocular lymphoma), it can be categorized as either:. -- Intraocular lymphoma, ... MedScape, Ocular lymphoma Karma A et al. Primary intraocular lymphoma: improving the diagnostic procedure. Opthamology 2007 Jul ...
A case is presented of an intraocular T-cell lymphoma mimicking a ring melanoma of the iris and being the first manifestation ... Intraocular T-cell lymphoma mimicking a ring melanoma. First manifestation of systemic disease. Report of a case and survey of ... A case is presented of an intraocular T-cell lymphoma mimicking a ring melanoma of the iris and being the first manifestation ... Further examination later showed T-cell lymphoma in the bone marrow, the only other organ involved. The patient died in a ...
... is the most common type of ocular lymphoma. Depending on the site of involvement, ocular lymphoma can be either intraocular or ... Whereas Hodgkin lymphoma very rarely causes ocular disease, non-Hodgkin lymphoma (NHL) ... Intraocular lymphoma. There are two distinct forms of intraocular lymphoma. When the ocular disease appears to be a subset of ... Intraocular lymphoma (IOL) is a rare lymphocytic malignancy. It may be either a primary intraocular lymphoma (PIOL) or a ...
"Intraocular Lymphoma" by people in this website by year, and whether "Intraocular Lymphoma" was a major or minor topic of these ... "Intraocular Lymphoma" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical ... Below are the most recent publications written about "Intraocular Lymphoma" by people in Profiles. ... Below are MeSH descriptors whose meaning is more general than "Intraocular Lymphoma". ...
... is the most common type of ocular lymphoma. Depending on the site of involvement, ocular lymphoma can be either intraocular or ... Whereas Hodgkin lymphoma very rarely causes ocular disease, non-Hodgkin lymphoma (NHL) ... Intraocular lymphoma. There are two distinct forms of intraocular lymphoma. When the ocular disease appears to be a subset of ... Intraocular lymphoma (IOL) is a rare lymphocytic malignancy. It may be either a primary intraocular lymphoma (PIOL) or a ...
Primary Intraocular Lymphoma. Primary intraocular lymphoma (lymphoma of the eye) is a cancer that involves the bodys white ... Lymphoma of the eye is a non-Hodgkins B cell lymphoma.. Most people with lymphoma of the eye are elderly or have problems that ... Lymphoma of the eye often happens with primary central nervous system lymphoma (PCNSL), which is lymphoma of the brain. ... blood cells (lymphocytes). Lymphomas can also start in organs such as the lungs, stomach, and rarely, the eyes. ...
Simultaneous Intraocular and Orbital Non-Hodgkin Lymphoma in the Acquired Immune Deficiency Syndrome. ... Dive into the research topics of Simultaneous Intraocular and Orbital Non-Hodgkin Lymphoma in the Acquired Immune Deficiency ...
... diffuse histiocytic lymphoma, and microglioma. The proliferation of names reflects initial uncertainty about the cell of origin ... Primary central nervous system lymphoma (PCNSL) has been known by many other names, including reticulum cell sarcoma, ... Primary intraocular lymphoma can be treated with systemic chemotherapy or intravitreal chemotherapy with or without ocular ... Primary intraocular lymphoma. Surv Ophthalmol. 2014 Sep-Oct. 59 (5):503-16. [QxMD MEDLINE Link]. ...
Intraocular lymphoma: Eye cancer that starts in the bodys infection-fighting cells (lymphocytes) ...
The most common intraocular cancers in adults are melanoma and lymphoma. The most common eye cancer in children is ... Treatment of Intraocular (Uveal) Melanoma (National Cancer Institute) Also in Spanish * Treatment Option Overview (Intraocular ... Stages of Intraocular (Uveal) Melanoma (National Cancer Institute) Also in Spanish * Stages of Retinoblastoma (National Cancer ... Childhood Intraocular (Uveal) Melanoma Treatment (National Cancer Institute) Also in Spanish * Retinoblastoma (National Eye ...
The main types of eye cancer are intraocular lymphoma, melanoma, retinoblastoma and hemangiomas. ...
Animals with intraocular lymphoma represented 0.19% of all patients with uveitis; animals with conjunctival lymphoma ... Prognosis seemed to be better for animals with conjunctival lymphoma than it was for those with intraocular lymphoma. ... Treatments included enucleation (4 intraocular) and chemotherapy (3 intraocular and 2 conjunctival). All dogs with intraocular ... and animals with intraocular lymphoma. Median PFST and OST for animals with conjunctival lymphoma were 221 and 549 days, ...
Intraocular Lymphoma.- *Update on Management of Coats Disease.- * Management of Choroidal Hemangioma. ... host disease, squamous cell neoplasia, intraocular lymphoma, coats disease, and choroidal hemangioma. Each chapter is written ...
Russell Read discusses uveitis masquerade syndromes including primary central nervous system intraocular lymphoma, leukemia, ...
Finally, one must consider neoplastic causes such as primary intraocular lymphoma, which may masquerade as a variety of ...
... are relatively rare and this is the first report stressing the ... Woolf DK, Ahmed M, Plowman PN (2012) Primary lymphoma of the ocular adnexa (orbital lymphoma) and primary intraocular lymphoma ... In light of the patients orbital lymphoma and the solitary ciliary body mass, a presumptive diagnosis of intraocular lymphoma ... Coexistence of orbital and intraocular lymphoma is extremely rare. A review of 110 medical records of lymphoma from the ...
In addition, ocular oncologists perform intravitreal injections of MMC for intraocular lymphoma, among other esoteric ... Phakic implantation of a black intraocular lens in a blind eye with leukocoria. J Cataract Refract Surg. 2003;29(4):839-841. ... Infectious postoperative endophthalmitis is a rare but catastrophic complication of intraocular surgery. Its incidence after ... they help create a barrier against the intraocular extension of some infections.4 ...
... is the most common type of ocular lymphoma. Depending on the site of involvement, ocular lymphoma can be either intraocular or ... Whereas Hodgkin lymphoma very rarely causes ocular disease, non-Hodgkin lymphoma (NHL) ... Intraocular lymphoma. There are 2 distinct forms of intraocular lymphoma. When the ocular disease appears to be a subset of ... In these cases, intraocular lymphoma can precede CNS involvement by months or years. The second form of intraocular lymphoma ...
... intraocular lymphoma and radiation side effects.. Dr. Sonal Chaugule, a recent fellow who trained under Dr. Paul Finger at the ... Thus, the angled technique delivers a more accurate dose as well as prevents intraocular infection by closing a potential entry ... The researchers found that the angled IVT injection technique had a significantly higher mean intraocular pressure immediately ... skills in RetCam operation for outpatient clinics as well as B-scan eye ultrasound for patients with suspicious intraocular ...
Intraocular Lymphoma with Retrobulbar Infiltration. A Case Report. Jurenová D. - Plesníková P. - Lysková D. - Babál P. - ...
Diagnosis and Treatment of Intraocular Malignant Lymphoma. Diagnosis and treatment of vitreoretinal lymphoma. *日本語 ... Diagnosis and treatment of vitreoretinal lymphoma. [email protected]. 〒113-8655. 3-1 Hongo, Bunkyo-ku, Tokyo. TEL:03-3815-5411(ext ... Treatment aims to treat intraocular and retinal diseases to restore patients visions and lower the number of deaths by ...
25-gauge transconjunctival sutureless vitrectomy for the diagnosis of intraocular lymphoma. Yeh, S., Weichel, E. D., Faia, L. J ... Canfield, V. A., Vose, J., Guiney, P., Bennett, B. & Nichols, C., 1997, In: Leukemia and Lymphoma. 24, 3-4, p. 335-339 5 p.. ... 2-Hydroxyethylnitrosourea induction of B cell lymphoma in female Swiss mice. Mirvish, S. S., Weisenburger, D. D., Joshi, S. S. ... 2-Chlorodeoxyadenosine as initial therapy for advanced low grade lymphomas. ...
Intraocular lymphoma. Adult, typically middle-aged or older. Metastatic cancer. Any, tends toward adults. ... The most critical question in evaluating a patient with intraocular inflammation is whether the disease can be classified into ... uveitis refers to a group of heterogeneous diseases that share the features of intraocular inflammation but whose etiologies ...
Successful use of semi-nested PCR for the diagnosis of primary intraocular lymphoma. Feilmeier, M. R., Lossos, I. S., Malumbres ... Superior efficacy of a combined epigenetic therapy against human mantle cell lymphoma cells. Fiskus, W., Rao, R., Balusu, R., ... R., Schefler, A. C. & Murray, T. G., Sep 15 2008, In: Leukemia and Lymphoma. 49, 8, p. 1612-1615 4 p.. Research output: ...
Intraocular Cancer Types. Uveal metastases are known as the most common type of intraocular cancer in adults that spreads to ... Conventional Surgery: The surgery involves making a new drainage canal to allow the intraocular fluid to drain out of the eye. ... The most common primary intraocular cancer seen in adults is Melanoma.. The reason of development of this cancer is the ...
Nonspecific term describing intraocular granulomatous inflammation. • Symptoms may include painful red eye, photophobia and ... Intraocular lymphoma. • Chronic retinal detachment. • Phacoanaphylactic glaucoma. TREATMENT. MEDICATION. First Line. • Topical ... Elevated intraocular pressure may necessitate a referral to glaucoma specialist.. • Development of cystoid macular edema (CME) ... Nonspecific term describing intraocular granulomatous inflammation.. • Symptoms may include painful red eye, photophobia and ...
Outlining uveal lymphoma, its clinical features, diagnostic process, and current treatment modalities. ... Uveal lymphoma is a subcategory of intraocular lymphoma. Intraocular lymphoma is categorized according to whether it ... Uveal lymphoma, is a subcategory of intraocular lymphoma that predominantly involves the uvea. This article will outline the ... Uveal lymphoma most typically arises from B-cell origin as a non-Hodgkins lymphoma. Primary uveal lymphoma can be further ...
Natural killer/T-cell lymphoma of nasal type with intraocular involvement: case report ... Modified transscleral fixation using combined temporary haptic externalization and injector intraocular lens implantation ...
This is called intraocular lymphoma.. Secondary CNS lymphoma is lymphoma that starts somewhere else in your body and spreads to ... Rarely, Burkitt lymphoma, T-cell lymphoma, or low-grade non-Hodgkin lymphomas can affect your CNS. CNS lymphoma can be either ... Lymphoma in the CNS is usually a fast-growing (high-grade) non-Hodgkin lymphoma. It is most often a form of diffuse large B- ... It includes lymphoma that is already in your CNS when you are diagnosed, as well as lymphoma that comes back (relapses) in your ...
  • Whereas Hodgkin lymphoma rarely causes ocular disease, non-Hodgkin lymphoma (NHL) is the most common type of ocular lymphoma. (medscape.com)
  • Depending on the site of involvement, ocular lymphoma can be intraocular, and adnexal. (medscape.com)
  • Hence, all patients with ocular lymphoma should have a complete workup to rule out systemic lymphoma. (medscape.com)
  • The prognosis for ocular lymphoma depends on the tumor's histologic type and stage and the treatment employed. (medscape.com)
  • The incidence of ocular lymphoma increases with advancing age. (medscape.com)
  • Objective -To determine prevalence, reason for evaluation, treatment, and outcome for dogs and cats with presumed solitary ocular lymphoma (PSOL). (avma.org)
  • Recent molecular studies demonstrating viral DNA in the ocular lymphoma cells suggest a role for infectious agents in the pathogenesis of intraocular lymphoma. (medscape.com)
  • Primary ocular lymphoma should be considered in persons older than 50 years with persistent intermediate or posterior uveitis that does not respond to anti-inflammatory therapy. (aafp.org)
  • Ocular lymphoma stems from lymphocytes (a type of white blood cells ) dividing and growing uncontrollably. (healthprep.com)
  • This entry looks at intraocular lymphoma, known as primary intraocular lymphoma (PIOL), one of the subtypes of lymphoma. (lymphomainfo.net)
  • These are known as primary intraocular cancers with melanoma being the most common form in adults. (opticalmasters.com)
  • Accounting for approximately 10% of blindness in the USA, uveitis refers to a group of heterogeneous diseases that share the features of intraocular inflammation but whose etiologies include idiopathic autoimmune disease, infections, rheumatologic diseases and masquerade syndromes. (medscape.com)
  • [ 1-3 ] The most critical question in evaluating a patient with intraocular inflammation is whether the disease can be classified into a specific, defined syndrome. (medscape.com)
  • Nonspecific term describing intraocular granulomatous inflammation. (entokey.com)
  • Intraocular pressure (IOP): Usually decreased because inflammation of the ciliary body causes decreased production of aqueous humor. (entokey.com)
  • 1 Generalized intraocular inflammation is described as panuveitis, whereas inflammation centered in the optic nerve head with secondary peripapillary involvement is classified under posterior uveitis as neuroretinitis. (aafp.org)
  • Rare causes of floaters include intraocular tumors (eg, lymphoma) and vitritis (inflammation of the vitreous). (msdmanuals.com)
  • The electronic patient records from all patients presenting in our clinic between January, 1st 2002 and March, 1st 2007 were retrospectively searched for diagnoses indicating intraocular inflammation. (openophthalmologyjournal.com)
  • Data analysis comprised two steps: Firstly, a database search was done for all relevant diagnoses that were indicative of intraocular inflammation, e.g. cystoid macular edema. (openophthalmologyjournal.com)
  • The search also included systemic diseases known to be associated with intraocular inflammation, e.g. sarcoidosis. (openophthalmologyjournal.com)
  • Typically, if a diagnosis of intraocular lymphoma is made, then it is followed by a complete neurological work-up to see if there is any CNS involvement or not. (lymphomainfo.net)
  • Diagnosis often is based on obtaining an intraocular biopsy specimen. (medscape.com)
  • From an initial retrospective review of 1543 patients with a diagnosis of intraocular and/or orbital spaceoccupied lesions, 8 patients (4 males and 4 females) with a coexistence of both intraocular and orbital mass lesions were identified. (omicsonline.org)
  • Based upon these findings, the presence of a lesion involving both the orbit and eye should be included when a diagnosis of retinoblastoma, idiopathic inflammatory pseudotumor, lymphoma, and/or Sturge- Weber syndrome is proposed. (omicsonline.org)
  • Immunocytology can also aid in the diagnosis given that the majority of uveal lymphomas are of B-cell origin, they should express B-cell antigens such as CD20, CD79a or PAX5. (eyewiki.org)
  • Dr Chan and her team recently published their data in one of the top Haematology journals demonstrating a novel technique that not only aids in early diagnosis of intraocular lymphomas but also enables her team to identify each individual's chemotherapy approach. (snec.com.sg)
  • Bottaro MBerti EBiondi AMigone NCrosti L Heteroduplex analysis of T-cell receptor gamma gene rearrangements for diagnosis and monitoring of cutaneous T-cell lymphomas. (jamanetwork.com)
  • The main types of eye cancer are intraocular lymphoma, melanoma, retinoblastoma and hemangiomas. (cancercare.org)
  • Patients' ages ranged from 22 months to 71 years (median = 3.0 years) and included 5 cases of retinoblastoma, 1 case of idiopathic inflammatory pseudotumor, 1 case of T-cell lymphoma, and 1 case of Sturge- Weber syndrome. (omicsonline.org)
  • Retinoblastoma in children and uveal melanoma in adults represent two of the most common primary intraocular tumor s [ 1 , 2 ]. (omicsonline.org)
  • In children, retinoblastoma (cancer that starts in cells in the retina) is the most common primary intraocular cancer. (opticalmasters.com)
  • While the most common intraocular cancers in adults are melanoma and lymphoma, the most common in children is retinoblastoma, which starts in retinal cells. (uniqacare.com)
  • In addition, ocular oncologists perform intravitreal injections of MMC for intraocular lymphoma, among other esoteric vitreoretinal applications, none of which carries formal FDA labeling. (crstoday.com)
  • This type of lymphoma represents 1% of NHLs, 1% of intracranial tumors, and less than 1% of intraocular tumors. (medscape.com)
  • PCNSL occurs at an incidence of 0.47 per 100,000 person-years, accounting for 4%-6% of extranodal lymphomas and 4% of newly diagnosed CNS tumors. (medscape.com)
  • This type of lymphoma is estimated to represent 1% of NHLs, 1% of intracranial tumors, and less than 1% of intraocular tumors. (medscape.com)
  • Lymphocytic markers applied to the biopsy specimen and to the enucleated eye revealed a highly malignant T-cell lymphoma infiltrating the iris, ciliary body, anterior choroid, retina and the adjacent vitreous body. (nih.gov)
  • PIOL is a subset of primary central nervous system lymphoma (PCNSL). (wikipedia.org)
  • PCNSL (and PIOL) are most commonly a diffuse large B-cell immunohistologic subtype of non-Hodgkin's lymphoma according to the World Health Organization (WHO) classification of lymphomas. (wikipedia.org)
  • Most cases of PIOL eventuate to central nervous system involvement (PCNSL) while only 20% of PCNSL lead to intraocular (PIOL) involvement. (wikipedia.org)
  • It can also be a secondary site, and therefore be considered a subtype of primary central nervous system lymphoma (PCNSL), and this is in fact the biggest concern with intraocular lymphoma-that it is found to have spread from the central nervous system (CNS). (lymphomainfo.net)
  • PIOL is mainly a subtype of primary CNS lymphoma (PCNSL). (medscape.com)
  • Lymphoma of the eye often happens with primary central nervous system lymphoma (PCNSL), which is lymphoma of the brain. (aao.org)
  • Primary central nervous system lymphoma (PCNSL) has been known by many other names, including reticulum cell sarcoma, diffuse histiocytic lymphoma, and microglioma. (medscape.com)
  • The DLBCL type of primary central nervous system lymphoma (PCNSL) is composed of immunoblasts or centroblasts that have a predilection for blood vessels and thus demonstrate a typical angiocentric growth pattern. (medscape.com)
  • Image 4: OCT imaging showing a lumpy bumpy choroid at presentation in a patient with uveal lymphoma. (eyewiki.org)
  • The most common intraocular cancers in adults are melanoma and lymphoma. (medlineplus.gov)
  • Apart from melanoma and lymphoma, other types of eye cancer affect the outer parts of the eyes. (healthprep.com)
  • It may be either a primary intraocular lymphoma (PIOL) or a secondary intraocular lymphoma (SIOL). (medscape.com)
  • Secondary intraocular cancers don't start in the eye itself but originate elsewhere in the body. (opticalmasters.com)
  • primary and secondary intraocular cancers. (healthprep.com)
  • Secondary intraocular cancers do not originate from inside the eye. (healthprep.com)
  • Intraocular lymphoma may affect the eye secondarily from a metastasis from a non-ocular tumor or may arise within the eye primarily (primary intraocular lymphoma, PIOL). (wikipedia.org)
  • Lymphoma' is an umbrella term that loosely refers to several dozen independent categorical types and subtypes of cancers of the lymphatic system. (lymphomainfo.net)
  • This may include intraocular melanomas, although not yet proven. (uniqacare.com)
  • immunophenotype of 2 uveal lymphomas was not determined. (avma.org)
  • Furthermore, adjunctive testing including polymerase chain reaction (PCR) amplification to identify monoclonal rearrangements of the immunoglobulin heavy chain (IgH) gene (for B-cell lymphomas) or T-cell receptor (TCR, for the very rare T-cell lymphomas) can be performed. (wikipedia.org)
  • Genotypic analysis of cutaneous T-cell lymphoma: a comparative study of southern blot analysis with polymerase chain reaction amplification of the T-cell receptor-gamma gene. (jamanetwork.com)
  • Diss TCWatts MPan LXBurke MLinch DIsaacson PG The polymerase chain reaction in the demonstration of monoclonality in T-cell lymphomas. (jamanetwork.com)
  • Scheller UMuche JMSterry WLukowsky A Detection of clonal T cells in cutaneous T-cell lymphoma by polymerase chain reaction: comparison of mutation detection enhancement-polyacrylamide gel electrophoresis, temperature gradient gel electrophoresis and fragment analysis of sequencing gels. (jamanetwork.com)
  • Tok JSzaboles MJSilvers DNZhong JMatsushima AY Detection of a clonal T-cell receptor gamma chain gene rearrangements by polymerase chain reaction and denaturing gradient gel electrophoresis (PCR/DGGE) in archival specimens from patients with early cutaneous T-cell lymphoma: correlation of histologic findings with PCR/DGGE. (jamanetwork.com)
  • A retrospective review was performed on cases of Chinese patients with clinical findings of simultaneous intraocular and orbital spaceoccupied lesions. (omicsonline.org)
  • Primary uveal lymphoma can be further classified by its location as choroidal, iridal, or ciliary body lymphoma. (eyewiki.org)
  • Also see Non-Hodgkin Lymphoma . (medscape.com)
  • Several hypotheses explain the increasing incidence of non-Hodgkin lymphoma (NHL). (medscape.com)
  • Lymphoma in the CNS is usually a fast-growing (high-grade) non-Hodgkin lymphoma. (jabalpurchronicle.org)
  • Rarely, Burkitt lymphoma, T-cell lymphoma, or low-grade non-Hodgkin lymphomas can affect your CNS. (jabalpurchronicle.org)
  • Primary non-Hodgkin lymphoma of the bladder (PNHLB) is extremely rare with only 110 cases identified in the medical literature. (bjuinternational.com)
  • Primary non-Hodgkin lymphoma of the bladder (PNHLB) represents less than 1% of all bladder neoplasms and between 0.15% and 0.2% of all extra-nodal lymphomas [7]. (bjuinternational.com)
  • Primary Hodgkin lymphoma and T-cell lymphoma are exceedingly rare. (bjuinternational.com)
  • Intraocular lymphoma is categorized according to whether it predominantly involves the retina or the uvea. (eyewiki.org)
  • Orbital and adnexal lymphoma is associated with systemic lymphoma in 30-35% of cases. (medscape.com)
  • The median age at presentation for orbital and adnexal lymphoma is older than 60 years. (medscape.com)
  • Concomitant intraocular and orbital space-occupied lesions are relatively rare and this is the first report stressing the underlying causes of concomitant intraocular and intraorbital lesions . (omicsonline.org)
  • In this paper, we present cases showing both intraocular and orbital soft tissue masses and highlight their clinical, pathological and imaging features. (omicsonline.org)
  • A retrospective review was performed on cases with both intraocular and orbital spaceoccupied lesions who were treated at the Zhongshan Ophthalmic Center, of Sun Yat-sen University, China between Jan 1, 2000 and Dec 31, 2011. (omicsonline.org)
  • Patients demonstrating a concomitant intraocular and orbital spaceoccupied lesion are relatively rare [ 4 , 5 ] and, to the best of our knowledge, this is the first report stressing the underlying causes of concomitant intraocular and intraorbital lesions in the literature. (omicsonline.org)
  • Extramarginal zone lymphomas, which account for most primary orbital and adnexal lymphomas, are characterized by an indolent natural history with frequent, continuous extranodal relapses. (medscape.com)
  • Treatments included enucleation (4 intraocular) and chemotherapy (3 intraocular and 2 conjunctival). (avma.org)
  • PURPOSE: Phase II trial to study the effectiveness of combining rituximab with combination chemotherapy given with osmotic blood-brain barrier disruption plus sodium thiosulfate in treating patients who have refractory or recurrent primary CNS lymphoma. (survivornet.com)
  • If the cancer starts inside the eyeball it's called intraocular cancer. (medlineplus.gov)
  • This is lymphoma that begins to grow in the eyeball. (opticalmasters.com)
  • When cancer starts in the eyeball, it is called primary intraocular cancer. (uniqacare.com)
  • Eye cancer is a rare tumor that can affect the outer parts of the eye (such as the eyelid) or the inside of the eyeball (intraocular cancer). (uniqacare.com)
  • [ 4 ] Clinical outcomes differ by histologic subtype with 5-year overall survival rates ranging from 30% in DLBCL to 79% in marginal zone lymphoma. (medscape.com)
  • Intraocular lymphoma is a rare malignant form of eye cancer. (wikipedia.org)
  • The incidence of lymphoproliferative ocular diseases, especially malignant lymphoma, has increased over the years. (medscape.com)
  • Central nervous system (CNS) lymphoma is a disease in which malignant (cancer) cells form in the lymph tissue of the brain and spinal cord. (jabalpurchronicle.org)
  • A case is presented of an intraocular T-cell lymphoma mimicking a ring melanoma of the iris and being the first manifestation of systemic disease. (nih.gov)
  • Veelken HWood GSSklar J Molecular staging of cutaneous T-cell lymphoma: evidence for systemic involvement in early disease. (jamanetwork.com)
  • [ 10 ] Intraocular lymphoma typically affects elderly patients, with reported series having mean ages in the seventh decade of life. (medscape.com)
  • Corticosteroids have a cytotoxic effect on lymphoma cells and can induce a radiographic response in up to half of patients, which limits the sensitivity of diagnostic tools like biopsy or lumbar puncture. (medscape.com)
  • Results -Animals with intraocular (4 dogs and 1 cat) or conjunctival (3 dogs and 1 cat) lymphoma represented 0.1% and 0.08% of patients with lymphoma evaluated at the hospital during the study period, respectively. (avma.org)
  • animals with conjunctival lymphoma represented 0.16% of all patients with conjunctivitis. (avma.org)
  • Lymph node metastasis was detected in 2 patients with conjunctival lymphoma. (avma.org)
  • Treatment aims to treat intraocular and retinal diseases to restore patients' visions and lower the number of deaths by reducing the incidence rate of CNS relapse. (iol.link)
  • Long-term follow-up of intraocular pressure and pressure-lowering medication in patients after ab-interno trabeculectomy with the Trabectome. (online.de)
  • Dynamic Contour Tonometry, Tono-Pen XL®, and Goldmann Applanation Tonometry in Comparison to Intracameral Intraocular Pressure (IOP) Measurements in Patients with Corneal Pathologies. (online.de)
  • Comparative measurement of intraocular pressure by Icare tonometry and Airpuff tonometry in healthy subjects and patients wearing therapeutic soft contact lenses. (online.de)
  • Determine the efficacy of rituximab, carboplatin, cyclophosphamide, etoposide or etoposide phosphate and cytarabine administered in conjunction with osmotic blood-brain barrier disruption and high-dose sodium thiosulfate, in terms of complete response rate, in patients with refractory or recurrent primary CNS lymphoma. (survivornet.com)
  • Previous cases of T-cell lymphoma with ocular involvement are reviewed. (nih.gov)
  • Intraocular T-cell lymphoma mimicking a ring melanoma. (nih.gov)
  • Further examination later showed T-cell lymphoma in the bone marrow, the only other organ involved. (nih.gov)
  • Lymphoma of the eye is a non-Hodgkin's B cell lymphoma. (aao.org)
  • [ 6 ] Follicular lymphoma, diffuse large B cell lymphoma, mantle cell lymphoma, B-cell chronic lymphocytic leukemia, peripheral T-cell lymphoma, and natural killer cell lymphoma have also been reported to affect the orbit. (medscape.com)
  • It is most often a form of diffuse large B-cell lymphoma. (jabalpurchronicle.org)
  • Pathology revealed a WHO grade 2 follicle centre cell lymphoma expressing CD20, CD10, BCL-2 and BCL-6 ( Fig 2 ). (bjuinternational.com)
  • [ 6 ] Additionally, a biopsy of lymphoma pre-treated with corticosteroids may reveal only gliosis or lymphocytic and histiocytic infiltrates without identifiable neoplastic cells. (medscape.com)
  • Better imaging techniques, improved biopsy techniques, and newer classification systems are likely to have contributed to the apparent increase in the incidence of lymphoma. (medscape.com)
  • Uveal lymphoma most typically arises from B-cell origin as a non-Hodgkin's lymphoma. (eyewiki.org)
  • The most common form of primary intraocular cancer in adults is melanoma, followed by lymphoma. (uniqacare.com)
  • Over the years, different systems have been used to classify lymphomas, including the Rappaport Classification (used until the 1970s), the Working Formulation, the National Cancer Institute Working Formulation, and the Revised European-American Lymphoma Classification (REAL). (medscape.com)
  • this represents the first worldwide consensus document on lymphoma classification. (medscape.com)
  • [12] . Secondary classification occurs with an intraocular manifestation of disseminated disease. (eyewiki.org)
  • Most cases were published before 1999 and are described in terms of the older "working classification" for lymphoma, with immunohistochemistry performed in less than 20% of cases [8]. (bjuinternational.com)
  • the remaining 10% are T-cell, mantle cell, Burkitt, or indolent B-cell lymphomas. (medscape.com)
  • Median PFST and OST for animals with conjunctival lymphoma were 221 and 549 days, respectively. (avma.org)
  • The most common presentation of intraocular lymphoma is decreased vision with non-resolving uveitis. (medscape.com)
  • The most common presentation of intraocular lymphoma is decreased vision with nonresolving uveitis. (medscape.com)
  • DelveInsight's "CNS Lymphoma - Market Insights, Epidemiology, and Market Forecast-2032" report delivers an in-depth understanding of the BP, historical and forecasted epidemiology as well as the BP market trends in the United States, the EU4, and the UK, and Japan. (jabalpurchronicle.org)
  • Primary choroidal lymphoma accounts for the majority of cases and is most frequently a low-grade lymphoma. (eyewiki.org)
  • One hallmark of a choroidal lymphoma is the presence of extra-scleral extension of the choroidal mass, which is often seen with ultrasound imaging. (eyewiki.org)
  • Images 1 and 2 demonstrate choroidal thickening, choroidal folds, and hyper-autofluorescent flecks in the macula in a patient presenting with uveal lymphoma. (eyewiki.org)
  • Primary intraocular lymphoma (lymphoma of the eye) is a cancer that involves the body's white blood cells (lymphocytes). (aao.org)
  • Intraocular foreign bodies can cause floaters but usually manifest with other symptoms, such as loss of vision, eye pain, or redness. (msdmanuals.com)
  • Glaucoma leads to vision loss and increases intraocular pressure. (medpersia.com)
  • The trabectome as treatment option in secondary glaucoma due to intraocular lymphoma. (online.de)
  • Recovery of corneal hysteresis after reduction of intraocular pressure in chronic primary angle-closure glaucoma. (online.de)
  • Lymphomas can also start in organs such as the lungs, stomach, and rarely, the eyes. (aao.org)
  • Primary intraocular lymphoma: improving the diagnostic procedure. (lymphomainfo.net)
  • Retinoblastomas are the most common form of primary intraocular cancer in children. (uniqacare.com)
  • Landa NGZelickson BDPeters MSMuller SAPittelkow MR Lymphoma versus pseudolymphoma of the skin: gene rearrangement study of 21 cases with clinicopathologic correlation. (jamanetwork.com)
  • Due to the rarity of disease, there is limited information regarding the typical features of uveal lymphoma. (eyewiki.org)
  • Most people with lymphoma of the eye are elderly or have problems that weaken the immune system, such as AIDS . (aao.org)
  • Having a weakened immune system may increase the risk of developing primary CNS lymphoma. (jabalpurchronicle.org)