Development of lesions in the lymph node characterized by infiltration of the cortex or paracortex by large collections of proliferating histiocytes and complete or, more often, incomplete necrosis of lymphoid tissue.
Inflammation of the lymph nodes.
Macrophages found in the TISSUES, as opposed to those found in the blood (MONOCYTES) or serous cavities (SEROUS MEMBRANE).
Infection of the lymph nodes by tuberculosis. Tuberculous infection of the cervical lymph nodes is scrofula.
They are oval or bean shaped bodies (1 - 30 mm in diameter) located along the lymphatic system.
INFLAMMATION of LYMPH NODES in the MESENTERY.
A fulminating bacterial infection of the deep layers of the skin and FASCIA. It can be caused by many different organisms, with STREPTOCOCCUS PYOGENES being the most common.

Recurrence of Kikuchi's lymphadenitis after 12 years. (1/60)

A 40 year old woman developed recurrent Kikuchi's disease 12 years after the original episode. The recurrence affected the same site (axilla) and occurred after the longest delay so far recorded in a European resident. Care must be taken to avoid misdiagnosis of Kikuchi's disease as lymphoma.  (+info)

Virus infection in patients with histiocytic necrotizing lymphadenitis in Taiwan. Detection of Epstein-Barr virus, type I human T-cell lymphotropic virus, and parvovirus B19. (2/60)

The relationship of Epstein-Barr virus (EBV), type I human T-cell lymphotropic virus (HTLV-I), and parvovirus B19 to histiocytic necrotizing lymphadenitis was studied prospectively in 10 Taiwanese patients using materials obtained by fine-needle aspiration and lymph node biopsy. The presence of EBV was detected by in situ hybridization for EBV-encoded RNA expression. Immunocytochemistry was used to detect virus-encoded protein for EBV and parvovirus B19. DNA in situ hybridization and polymerase chain reaction were performed to determine the existence of HTLV-I provirus. Expressions of EBV-encoded RNA and Fas ligand were detected in all cases. Expression of EBV-encoded protein was identified in only 1 case. Neither HTLV-I nor parvovirus B19 was detected in any case.  (+info)

Haemophagocytic syndrome and histiocytic necrotising lymphadenitis (Kikuchi's disease). (3/60)

A young boy presented with a rash, fever, and cervical lymphadenopathy, originally thought to be caused by tuberculosis. A lymph node biopsy showed the features of Kikuchi's disease, with necrosis and histiocytic infiltration without neutrophils. No evidence of tuberculosis was found on staining, culture, or the polymerase chain reaction. Bone marrow biopsy revealed prominent haemophagocytosis, and a diagnosis of haemophagocytic syndrome was reached. The aetiology of haemophagocytic syndrome, and its association with Kikuchi's lymphadenitis, is discussed.  (+info)

An unusual case of pyrexia of unknown origin with cervical lymphadenopathy. (4/60)

Kikuchi's disease is usually a self limiting illness characterised by pyrexia, neutropenia, and cervical lymphadenopathy particularly in young women of Asian descent. This often leads to an initial misdiagnosis of lymphoma. A case of a young Asian woman who presented with pyrexia of unknown origin is described.  (+info)

Myeloperoxidase expression by histiocytes in Kikuchi's and Kikuchi-like lymphadenopathy. (5/60)

Forty-five examples of Kikuchi's lymphadenitis (KL), 5 Kikuchi-like lupus erythematosus lymphadenopathies, 25 nonnecrotizing lymphadenitidies (5 toxoplasmic, 5 sarcoid-like, 6 dermatopathic, 4 suppurative, 3 tubercular, 2 with sinus histiocytosis), 4 examples of hyaline-vascular Castleman disease (CD), 2 plasmacytoid monocyte tumors (PM-Ts), and 61 accessory cell neoplasms were studied by a panel of antibodies, including the PG-M1 (against a macrophage-restricted CD68 epitope) and a polyclonal anti-myeloperoxidase (MPO). In KL and Kikuchi-like lupus erythematosus lymphadenopathies, 25 to 75% of CD68(+) histiocytes co-expressed MPO. This did not occur in nonnecrotizing lymphadenitidies and accessory cell neoplasms. MPO(+)/CD68(+) elements corresponded to nonphagocytosing mononuclear cells and some crescentic macrophages and phagocytosing histiocytes. Typical PMs were MPO(-)/CD68(+) in all cases, including CD and PM-T. Our observations suggest that in KL and KL-like lymphadenopathies: 1) MPO(+)/CD68(+) blood monocytes might be attracted into tissues because of the lack or paucity of granulocytes and the need of MPO for oxidative processes; 2) PMs are more likely to be involved in the cytotoxic immune reaction than in phagocytic phenomena; 3) the peculiar phenotype of the histiocytic component can be usefully used for the differentiation from malignant lymphoma and PM-T.  (+info)

Immediate remission obtained by minocycline in a patient with histiocytic necrotizing lymphadenitis. (6/60)

A 29-year-old man was admitted because of fever, arthralgia and swelling of the cervical lymph nodes. A diagnosis of histiocytic necrotizing lymphadenitis (HNL) was made based on the findings of a lymph node biopsy. At first, piperacillin sodium (PIPC) was started, but a spiking fever persisted. We therefore changed the PIPC treatment to minocycline. On the following day, his clinical and laboratory findings were dramatically improved. After administering minocycline for 10 days, the HNL symptoms completely disappeared. He has been in good health for 3 years since undergoing treatment. This case strongly indicates that minocycline-sensitive microorganism(s) may be related, at least in part, to the etiology of HNL.  (+info)

Spontaneous regression of Kikuchi lymphadenopathy with oligoclonal T-cell populations favors a benign immune reaction over a T-cell lymphoma. (7/60)

To aid in the initial diagnosis of Kikuchi lymphadenitis and to assess whether the composition of the T cells might shed light on the pathogenesis, we used nested polymerase chain reaction tests followed by high-resolution gel electrophoresis to determine the pattern of T-cell antigen receptor rearrangement in 56 consecutive cases. Except for 1 unusual case with recurrent lymphadenopathy, none had a monoclonal beta or gamma rearrangement. Eight cases had a polyclonal pattern at both beta and gamma loci, 20 cases had a mixed polyclonal beta and oligoclonal gamma pattern, and 27 cases had an oligoclonal pattern at both loci. The high frequency of oligoclonality did not indicate an early-stage T-cell lymphoma in evolution, as confirmed by spontaneous resolution of the lymphadenopathy in all cases within 6 months. Rather, it is consistent with reports of oligoclonal T cells in a variety of immune reactions. We conclude that, in the vast majority of cases, absence of a monoclonal T-cell receptor rearrangement excludes the possibility of T-cell lymphoma, and the presence of an oligoclonal pattern implies a benign immune reaction.  (+info)

Histiocytic necrotizing lymphadenitis (Kikuchi lymphadenitis) in an HIV-positive patient. (8/60)

Histiocytic necrotizing lymphadenitis, or Kikuchi's lymphadenitis (KL), is an unusual form of lymphadenitis, generally with self-limited clinical course. KL has been reported in rare patients infected with the human immunodeficiency virus (HIV). Pathogenesis of the lesion is probably related to an impaired immune function. The purpose of the present article is to report on one case in which KL was diagnosed in an HIV-infected patient. Histomorphology and immunophenotype were similar to previous reports, but a focus of activated CD30+ macrophages was seen, what might be due to the immunological status of the patient. EBV was not detected on the sections using the in situ hybridization technique. Although rare, the occurrence of KL in HIV-infected subjects must be emphasized, because of the potential misdiagnosis of malignancy, especially in the presence of CD30+ cells.  (+info)

Histiocytic Necrotizing Lymphadenitis is a condition characterized by the inflammation and necrosis (death of tissue) of lymph nodes, caused by an abnormal proliferation and activation of histiocytes (a type of white blood cell). It is also known as Kikuchi's disease. The exact cause of this condition is unknown, but it is thought to be related to an immune response to viral infections or other antigens.

Histopathologically, it is characterized by the presence of necrotizing granulomatous inflammation with histiocytic predominance and absence of neutrophils. The condition is typically self-limiting, with symptoms resolving within a few months without specific treatment. However, in some cases, it can be associated with systemic symptoms or other autoimmune disorders.

Lymphadenitis is a medical term that refers to the inflammation of one or more lymph nodes, which are small, bean-shaped glands that are part of the body's immune system. Lymph nodes contain white blood cells called lymphocytes, which help fight infection and disease.

Lymphadenitis can occur as a result of an infection in the area near the affected lymph node or as a result of a systemic infection that has spread through the bloodstream. The inflammation causes the lymph node to become swollen, tender, and sometimes painful to the touch.

The symptoms of lymphadenitis may include fever, fatigue, and redness or warmth in the area around the affected lymph node. In some cases, the overlying skin may also appear red and inflamed. Lymphadenitis can occur in any part of the body where there are lymph nodes, including the neck, armpits, groin, and abdomen.

The underlying cause of lymphadenitis must be diagnosed and treated promptly to prevent complications such as the spread of infection or the formation of an abscess. Treatment may include antibiotics, pain relievers, and warm compresses to help reduce swelling and discomfort.

Histiocytes are a type of immune cell that are part of the mononuclear phagocyte system. They originate from monocytes, which are derived from hematopoietic stem cells in the bone marrow. Histiocytes play an important role in the immune system by engulfing and destroying foreign substances, such as bacteria and viruses, as well as removing dead cells and other debris from the body. They can be found in various tissues throughout the body, including the skin, lymph nodes, spleen, and liver.

Histiocytes include several different types of cells, such as macrophages, dendritic cells, and Langerhans cells. These cells have different functions but all play a role in the immune response. For example, macrophages are involved in inflammation and tissue repair, while dendritic cells are important for presenting antigens to T cells and initiating an immune response.

Abnormal accumulations or dysfunction of histiocytes can lead to various diseases, such as histiocytosis, which is a group of disorders characterized by the abnormal proliferation and accumulation of histiocytes in various tissues.

Tuberculosis (TB) of the lymph node, also known as scrofula or tuberculous lymphadenitis, is a specific form of extrapulmonary tuberculosis. It involves the infection and inflammation of the lymph nodes (lymph glands) by the Mycobacterium tuberculosis bacterium. The lymph nodes most commonly affected are the cervical (neck) and supraclavicular (above the collarbone) lymph nodes, but other sites can also be involved.

The infection typically spreads to the lymph nodes through the bloodstream or via nearby infected organs, such as the lungs or intestines. The affected lymph nodes may become enlarged, firm, and tender, forming masses called cold abscesses that can suppurate (form pus) and eventually rupture. In some cases, the lymph nodes may calcify, leaving hard, stone-like deposits.

Diagnosis of tuberculous lymphadenitis often involves a combination of clinical evaluation, imaging studies (such as CT or MRI scans), and microbiological or histopathological examination of tissue samples obtained through fine-needle aspiration biopsy or surgical excision. Treatment typically consists of a standard anti-tuberculosis multi-drug regimen, which may include isoniazid, rifampin, ethambutol, and pyrazinamide for at least six months. Surgical intervention might be necessary in cases with complications or treatment failure.

Lymph nodes are small, bean-shaped organs that are part of the immune system. They are found throughout the body, especially in the neck, armpits, groin, and abdomen. Lymph nodes filter lymph fluid, which carries waste and unwanted substances such as bacteria, viruses, and cancer cells. They contain white blood cells called lymphocytes that help fight infections and diseases by attacking and destroying the harmful substances found in the lymph fluid. When an infection or disease is present, lymph nodes may swell due to the increased number of immune cells and fluid accumulation as they work to fight off the invaders.

Mesenteric lymphadenitis is a condition characterized by inflammation of the lymph nodes in the mesentery, which is the membrane that attaches the intestine to the abdominal wall. These lymph nodes are part of the immune system and help fight infection.

Mesenteric lymphadenitis can be caused by a variety of factors, including bacterial or viral infections, inflammatory bowel disease, or autoimmune disorders. In many cases, however, a specific cause cannot be identified. Symptoms may include abdominal pain, fever, nausea, vomiting, and diarrhea.

In most cases, mesenteric lymphadenitis is a self-limiting condition, which means that it will resolve on its own without treatment. However, in some cases, antibiotics may be necessary to treat an underlying infection. In rare cases, surgery may be required to remove severely inflamed or infected lymph nodes.

Necrotizing fasciitis is a serious bacterial infection that affects the fascia, which is the tissue that surrounds muscles, nerves, and blood vessels. The infection can also spread to the muscle and skin. It is often caused by a combination of different types of bacteria, including group A Streptococcus and Staphylococcus aureus.

The infection causes extensive tissue damage and necrosis (death) of the fascia and surrounding tissues. It can progress rapidly and can be fatal if not treated promptly with aggressive surgical debridement (removal of dead tissue) and antibiotics.

Symptoms of necrotizing fasciitis include severe pain, swelling, redness, and warmth in the affected area; fever; chills; and general weakness. It is important to seek medical attention immediately if these symptoms occur, as early diagnosis and treatment can significantly improve outcomes.

... generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. ... also called histiocytic necrotizing lymphadenitis or Kikuchi-Fujimoto disease, is an uncommon, idiopathic, ... Kikuchis histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn ... Kikuchis disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic ...
What is histiocytic necrotizing lymphadenitis? Read on to learn more about this rare condition, including its potential causes ... 2019). Histiocytic necrotising lymphadenitis.. https://dermnetnz.org/topics/histiocytic-necrotising-lymphadenitis. *. ... KFD is also known by other names, such as histiocytic necrotizing lymphadenitis or Kikuchi disease. KFD mainly. occurs in ... 2021). Kikuchi-Fujimoto disease: A rare cause of histiocytic necrotising lymphadenitis in young ethnic women.. https:// ...
2003). "Expression of apoptosis-associated protein RCAS1 in macrophages of histiocytic necrotizing lymphadenitis". Int. J. ...
... generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. ... also called histiocytic necrotizing lymphadenitis or Kikuchi-Fujimoto disease, is an uncommon, idiopathic, ... Kikuchis histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn ... Kikuchis disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic ...
... from 15 patients underwent histopathologic examination and revealed chronic necrotizing lymphadenitis with histiocytic ... Tularemia presenting as tonsillopharyngitis and cervical lymphadenitis: a case report and review of the literature. Eur Arch ...
Kikuchi lymphadenitis (ie, histiocytic necrotizing lymphadenitis) is a benign and rare disease of unknown origin that involves ... Cervical lymphadenitis in infants and children. Semin Pediatr Surg. 1994 Aug. 3 (3):134-41. [QxMD MEDLINE Link]. ... Atypical mycobacterial lymphadenitis in childhood--a clinicopathological study of 17 cases. J Clin Pathol. 1998 Dec. 51 (12): ... In Kawasaki disease (ie, mucocutaneous lymph node syndrome), lymphadenitis is one of the earliest aspects of the disease. The ...
MA DDF; HOLLIS RR; DELBRIDGE L, 1986, HISTIOCYTIC NECROTIZING LYMPHADENITIS (KIKUCHIS DISEASE), Australian and New Zealand ...
... histiocytic necrotizing lymphadenitis), metastatic nodes from a regional primary lymphoma, and tuberculous adenitis. Benign ...
Histiocytic Necrotizing Lymphadenitis Medicine & Life Sciences 74% * Seroconversion Medicine & Life Sciences 61% ... Kikuchi-Fujimoto disease with superimposed bacterial lymphadenitis. Burns, J., Pathania, S., Griesser, R., Norelli, J., ...
... histiocytic necrotizing lymphadenitis (Kikuchi lymphadenitis), sarcoidosis, immune thrombocytopenic purpura, solid organ ...
Histiocytic necrotizing lymphadenitis. In critically ill patients, measure-ment of serum calcium level is normal, proving that ...
Histiocytic necrotising lymphadenitis. 33%. Cognitive disorder. 33%. Dysuria. 33%. Pulmonary embolism. 33%. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LÍQUIDO CÍSTICO. CYST FLUID. LIQUIDO CISTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITE HISTIOCÍTICA NECROSANTE. LIQUIDO CISTICO. CYST FLUID. LÍQUIDO CÍSTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LÍQUIDO CÍSTICO. CYST FLUID. LIQUIDO CISTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITE HISTIOCÍTICA NECROSANTE. LIQUIDO CISTICO. CYST FLUID. LÍQUIDO CÍSTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LÍQUIDO CÍSTICO. CYST FLUID. LIQUIDO CISTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITE HISTIOCÍTICA NECROSANTE. LIQUIDO CISTICO. CYST FLUID. LÍQUIDO CÍSTICO. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
HISTIOCYTIC NECROTIZING LYMPHADENITIS. LINFADENITIS NECROTIZANTE HISTIOCITICA. LINFADENITE HISTIOCÍTICA NECROSANTE. HIV LONG- ... ENTEROCOLITIS, NECROTIZING. ENTEROCOLITIS NECROTIZANTE. ENTEROCOLITE NECROSANTE. ENTOMOPHTHORALES. ENTOMOPHTHORALES. ...
... generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. ... also called histiocytic necrotizing lymphadenitis or Kikuchi-Fujimoto disease, is an uncommon, idiopathic, ... Kikuchis histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn ... Kikuchis disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic ...
... generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. ... also called histiocytic necrotizing lymphadenitis or Kikuchi-Fujimoto disease, is an uncommon, idiopathic, ... Kikuchis histiocytic necrotizing lymphadenitis: an analysis of 108 cases with emphasis on differential diagnosis. Semin Diagn ... Kikuchis disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic ...

No FAQ available that match "histiocytic necrotizing lymphadenitis"

No images available that match "histiocytic necrotizing lymphadenitis"