Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells.
A disease of the pilosebaceous unit, presenting clinically as grouped follicular papules or plaques with associated hair loss. It is caused by mucinous infiltration of tissues, and usually involving the scalp, face, and neck. It may be primary (idiopathic) or secondary to mycosis fungoides or reticulosis.
Abnormal increase of EOSINOPHILS in the blood, tissues or organs.

A case of eosinophilic myocarditis complicated by Kimura's disease (eosinophilic hyperplastic lymphogranuloma) and erythroderma. (1/45)

This report describes a patient with eosinophilic myocarditis complicated by Kimura's disease (eosinophilic hyperplastic lymphogranuloma) and erythroderma. A 50-year-old man presented with a complaint of precordial pain. However, the only abnormal finding on examinatioin was eosinophilia (1617 eosinophils/microl). Three years later, the patient developed chronic eczema, and was diagnosed with erythroderma posteczematosa. One year later, a tumor was detected in the right auricule, and a diagnosis of Kimura's disease was made, based on the biopsy findings. The patient developed progressive dyspnea 6 months later and was found to have cardiomegaly and a depressed left ventricular ejection fraction (17%). A diagnosis of eosinophilic myocarditis was made based on the results of a right ventricular endomyocardial biopsy. The eosinophilic myocarditis and erythrodrema were treated with steroids with improvement of both the eosinophilia and left ventricular function.  (+info)

Kimura's disease with bilateral auricular masses. (2/45)

We report an unusual case of Kimura's disease. An 81-year-old Japanese woman was shown to have bilateral auricular masses that had begun to enlarge 6 years before. On CT scans, slightly high-density masses with faint contrast enhancement were seen. The masses were heterogeneous and hypointense on T1-weighted MR images, were slightly hyperintense on T2-weighted MR images, and showed heterogeneous enhancement after the administration of contrast material. Kimura's disease should be included in the differential diagnosis of bilateral auricular tumors.  (+info)

Life threatening coronary artery spasm in childhood Kimura's disease. (3/45)

A 13 year old boy is described with hypereosinophilia associated with Kimura's disease, who showed repeated life threatening syncopal attacks during daily activities or at rest. Coronary arteriography demonstrated small aneurysms with irregular vessel walls of both coronary arteries, and the absence of organic stenotic lesions. Infusion of a minimal dose of ergonovine into the right coronary artery induced severe spasm of the vessel. Ventricular fibrillation recurred even after administration of nifedipine and isosorbide was started, but was completely inhibited by prednisolone.  (+info)

Gray scale and power Doppler sonography in cases of Kimura disease. (4/45)

SUMMARY: Kimura disease is a rare chronic inflammatory disorder mimicking malignancy. Nodes are present in the submental and submandibular regions, within the parotid gland, and in the upper cervical chain. On gray scale sonograms, they are hypoechoic and round, with normal hilar architecture and homogeneous internal echoes. On power Doppler sonograms, the nodes show prominent intranodal vessels with a hilar pattern and low intranodal resistance. The soft tissue and parotid lesions also show low-resistance vascularity within.  (+info)

Bilateral orbital Kimura's disease in a young Asian man. (5/45)

A 16-year-old Asian man adolescent presented with bilateral eyelid swelling with multiple palpable mass lesions, which waned after treatment with corticosteroids but waxed after medications were discontinued, for about 1 year. He was otherwise healthy except that bilateral postauricular lymphadenopathy had developed for about 9 years. Laboratory study revealed peripheral eosinophilia with an elevated IgE level. The tumor masses of the left orbit were completely excised through an incision similar to that used in blepharoplasty, which gave good cosmetic results. Postoperative computed tomography scan showed no residual tumor mass in the left orbit but contralateral homogeneous soft-tissue mass lesions around the lacrimal gland and extending deep into the orbit, between the superior and lateral rectus muscles. Pathology reported numerous lymphoid follicles with active germinal centers and extensive lymphocyte and eosinophil infiltration, which characterize Kimura's disease (KD). The tumor mass in the right orbit was also excised during a second elective surgery 10 days later. No evidence of recurrence was noted after follow-up for 7 months. KD of the orbit is rare and usually occurs in middle-aged to elderly Asian men but can also be present in young adolescent. Complete excision with simultaneous blepharoplasty gives satisfactory cosmetic results.  (+info)

Bilateral Kimura's disease of the eyelids. (6/45)

A case of Kimura's disease affecting the eyelids bilaterally is reported in a 5-year-old boy of Afro-Caribbean extraction who has been followed for 12 years with repeat biopsies. He initially presented at 5 years of age with swelling of the left upper eyelid, left cervical lymphadenopathy, and eosinophilia. One year later he developed swelling of the right upper eyelid. There has been no change in the clinical appearance over the next 12 years. Repeated biopsies of the eyelids showed a diffuse inflammatory infiltrate with many eosinophils and lymphocytes. A lymph node biopsy showed reactive lymphoid hyperplasia. Immunohistochemistry using lymphoid markers showed a polyclonal pattern. Kimura's disease is a rare cause of eyelid swelling, particularly at such a young age and with bilateral involvement. This case demonstrates that bilateral orbital lymphoid lesions with cervical node involvement do not always imply lymphoma, but may have a benign pathogenesis. The unusually long follow up in this case confirms an excellent prognosis for Kimura's disease with conservative management. Accurate diagnosis in small orbital biopsies may spare the patient unnecessary radical surgery.  (+info)

Kimura's disease: a diagnostic and therapeutic challenge. (7/45)

INTRODUCTION: Kimura's disease (KD) is a rare, benign, chronic inflammatory disease with unknown aetiology. Its manifestation is protean. KD has a predilection for the head and neck area, and typically presents as tumour-like lesions that could be easily misdiagnosed. We review our experience with four recent cases. METHODS: Over a four-year period, all patients admitted to Singapore General Hospital with KD of the head and neck region were retrospectively reviewed. Biodata, presenting symptoms and clinical parameters, especially serum eosinophil levels, preoperative investigations, type of surgical procedures and outcome were documented. RESULTS: Four patients presented with KD of the head and neck and displayed varied manifestations of the disease. All the patients had raised serum eosinophil levels. None of them had renal involvement. Preoperative computed tomography were performed in two of the patients and showed features suggestive of KD. Fine-needle aspiration cytology that was performed in two patients was not useful in the diagnosis. All the patients underwent surgical excision of the lesions. Only one patient had multiple recurrence, both at the original and remote sites in the head and neck. CONCLUSION: The clinical presentation and behaviour of KD is very variable. Preoperative imaging is useful in the diagnosis of the disease but the final diagnosis is histological. Surgical excision is the current treatment of choice but recurrence is common. A high index of suspicion and awareness is vital in the early diagnosis and management of KD.  (+info)

Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma) of the lung: a clinicopathologic and immunohistochemical study of two cases. (8/45)

Two cases of primary angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma) (ALHE/EH) of the lung are described. Both patients are white, a 60-year-old man and a 27-year-old woman. One patient had a long-standing history of asthma, and the other had symptomatology related to the pulmonary mass. Wedge resections were performed in both cases, and both lesions shared similar histopathologic changes, mainly the presence of a tumor mass with a marked presence of eosinophils in the background, lymphoid hyperplasia, and marked proliferations of small-caliber vessels. Immunohistochemical studies using leukocyte common antigen, L-26, and UCHL-1 nicely stained the lymphoid component of the lesion, and CD31 clearly outlined the vascular component of the process. Clinical follow-up demonstrated that the woman died of status asthmaticus, and the man was alive and well 1 year after surgical resection of the lesion. Both cases highlight the ubiquitous distribution of ALHE/EH and underscore the importance of keeping these lesions in the differential diagnosis of vascular and lymphoid lesions of the lung.  (+info)

Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign vascular lesion that typically presents as one or multiple papules or nodules, often on the head and neck region. The exact cause of ALHE is unknown, but it has been associated with chronic inflammation and immune dysfunction.

Histologically, ALHE is characterized by the proliferation of blood vessels and lymphoid tissue, with a prominent infiltration of eosinophils. The lesions may also contain other inflammatory cells such as plasma cells, histiocytes, and T-lymphocytes.

Clinically, ALHE presents as red to brownish papules or nodules that can be tender or pruritic (itchy). Lesions typically occur on the head and neck region, particularly around the ears, eyes, and nose. In some cases, lesions may also appear on the trunk, arms, or legs.

While ALHE is a benign condition, it can cause significant cosmetic concerns due to its location. Treatment options include surgical excision, laser therapy, and intralesional corticosteroid injections. Recurrence after treatment is not uncommon. It is important to note that while ALHE may resemble other more serious conditions such as cutaneous lymphoma or angiosarcoma, it has a much more favorable prognosis.

Follicular mucinosis is a cutaneous condition characterized by the accumulation of mucin in the hair follicles. Mucin is a complex sugar-protein substance that provides cushioning and lubrication in various tissues throughout the body. In follicular mucinosis, there is an overproduction of mucin within the hair follicles, leading to visible bumps or papules on the skin.

Follicular mucinosis can be classified into three types: primary, secondary, and variant. The primary type is further divided into two subcategories: classic and atypical. The classic form of primary follicular mucinosis typically affects middle-aged adults and presents with localized or generalized patches of skin that are scaly, itchy, and have a smooth, shiny appearance (known as "alopetic pseudopelade"). In contrast, the atypical form is often associated with lymphoma.

Secondary follicular mucinosis can occur in association with various inflammatory skin conditions, such as eczema, psoriasis, and discoid lupus erythematosus. The variant type of follicular mucinosis is a rare condition that primarily affects children and adolescents, presenting with localized areas of thickened, rough skin (known as "hyperkeratotic").

The exact cause of primary follicular mucinosis remains unclear, but it is thought to involve an abnormal immune response. Secondary follicular mucinosis, on the other hand, is a reactive process triggered by underlying inflammatory skin conditions. Treatment for follicular mucinosis depends on the type and severity of the condition, ranging from topical corticosteroids to systemic immunosuppressive therapy in more severe cases.

Eosinophilia is a medical condition characterized by an abnormally high concentration of eosinophils in the circulating blood. Eosinophils are a type of white blood cell that play an important role in the immune system, particularly in fighting off parasitic infections and regulating allergic reactions. However, when their numbers become excessively high, they can contribute to tissue damage and inflammation.

Eosinophilia is typically defined as a count of more than 500 eosinophils per microliter of blood. Mild eosinophilia (up to 1,500 cells/μL) may not cause any symptoms and may be discovered during routine blood tests. However, higher levels of eosinophilia can lead to various symptoms such as coughing, wheezing, skin rashes, and organ damage, depending on the underlying cause.

The causes of eosinophilia are varied and can include allergic reactions, parasitic infections, autoimmune disorders, certain medications, and some types of cancer. Accurate diagnosis and treatment of eosinophilia require identification and management of the underlying cause.

... (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory ... a mimic of angiolymphoid hyperplasia with eosinophilia". Dermatology. 223 (4): 301-305. doi:10.1159/000335372. PMID 22269779. ...
Angiolymphoid hyperplasia with eosinophilia is a disorder initially classified as a form of IgG4-related diseases but now ... Guo R, Gavino AC (2015). "Angiolymphoid hyperplasia with eosinophilia". Archives of Pathology & Laboratory Medicine. 139 (5): ... "EOS eosinophilia, familial [Homo sapiens (human)] - Gene - NCBI". OMIM Entry - % 131400 - EOSINOPHILIA, FAMILIAL Klion AD, Law ... A parasitic infection of nearly any bodily tissue can cause eosinophilia.[citation needed] Diseases that feature eosinophilia ...
Jeon EK, Cho AY, Kim MY, Lee Y, Seo YJ, Park JK, Lee JH (February 2009). "Angiolymphoid hyperplasia with eosinophilia that was ... Akosa AB, Ali MH, Khoo CT, Evans DM (June 1990). "Angiolymphoid hyperplasia with eosinophilia associated with tetanus toxoid ... Hallam LA, Mackinlay GA, Wright AM (September 1989). "Angiolymphoid hyperplasia with eosinophilia: possible aetiological role ... Peripheral eosinophilia and the presence of eosinophils in the inflammatory infiltrate suggest it may be a hypersensitivity ...
Angiolymphoid hyperplasia with eosinophilia (or lesions that mimic it) and cutaneous pseudolymphoma Cutaneous plasmacytosis ... a mimic of angiolymphoid hyperplasia with eosinophilia". Dermatology. 223 (4): 301-305. doi:10.1159/000335372. PMID 22269779. ...
... a mimic of angiolymphoid hyperplasia with eosinophilia". Dermatology. 223 (4): 301-305. doi:10.1159/000335372. PMID 22269779. ... Approximately 1/3 of cases exhibit increases in blood eosinophil counts, either eosinophilia or hypereosinophilia.[citation ...
IgG4-related disease and Angiolymphoid hyperplasia with eosinophilia as well as non-hematologic cancers such as solid tumors of ... Clonal eosinophilia caused by mutations in genes that are highly susceptible to tyrosine kinase inhibitors such as PDGFRA, ... For example, an underlying malignant cause for the eosinophilia may be survival-limiting. In 1936, the famed Swiss physician ... The DRESS syndrome (Drug Reaction with Eosinophilia and Systemic Symptoms) is a severe immunological drug reaction. It differs ...
Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma, histiocytoid hemangioma, inflammatory angiomatous nodule, ... Spiegler-Fendt lymphoid hyperplasia, Spiegler-Fendt sarcoid) Cutaneous lymphoid hyperplasia with bandlike and perivascular ... patterns Cutaneous lymphoid hyperplasia with nodular pattern (nodular pattern of cutaneous lymphoid hyperplasia) Diffuse large ... focal epithelial hyperplasia) Hemorrhagic fever with renal syndrome Hepatitis B Hepatitis C Herpangina Herpes gladiatorum ( ...
... eosinophilia MeSH C15.378.553.231.085 - angiolymphoid hyperplasia with eosinophilia MeSH C15.378.553.231.335 - eosinophilia- ... angiolymphoid hyperplasia with eosinophilia MeSH C15.604.515.292.015 - Churg-Strauss syndrome MeSH C15.604.515.435 - heavy ... pulmonary eosinophilia MeSH C15.378.553.381 - infectious mononucleosis MeSH C15.378.553.475 - leukocytosis MeSH C15.378.553.475 ... giant lymph node hyperplasia MeSH C15.604.515.292 - granuloma MeSH C15.604.515.292.007 - ...
Angiolymphoid hyperplasia with eosinophilia (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory ... a mimic of angiolymphoid hyperplasia with eosinophilia". Dermatology. 223 (4): 301-305. doi:10.1159/000335372. PMID 22269779. ...
Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon idiopathic condition that manifests in adults as isolated or ... encoded search term (Angiolymphoid Hyperplasia With Eosinophilia) and Angiolymphoid Hyperplasia With Eosinophilia What to Read ... Angiolymphoid Hyperplasia With Eosinophilia. Updated: Apr 11, 2019 * Author: Gauri Panse, MBBS, MD; Chief Editor: William D ... Angiolymphoid hyperplasia with eosinophilia (ALHE) is uncommon but not rare; it may be more common in Japan than in other ...
Angiolymphoid hyperplasia with eosinophilia associated with hepatitis C antibodies ... Angiolymphoid hyperplasia with eosinophilia along… February 25, 2022 *Allopurinol-induced drug reaction with eosinophilia… June ... Angiolymphoid hyperplasia with eosinophilia (ALHE) was originally described by Wells and Whimster [1] in 1969. They considered ... Angiolymphoid hyperplasia with eosinophilia is an entity distinct from Kimura′s disease. With the advancement of staining ...
Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon idiopathic condition that manifests in adults as isolated or ... encoded search term (Angiolymphoid Hyperplasia With Eosinophilia) and Angiolymphoid Hyperplasia With Eosinophilia What to Read ... Angiolymphoid Hyperplasia With Eosinophilia. Updated: Jul 14, 2016 * Author: Sarah K Taylor, MD; Chief Editor: William D James ... Angiolymphoid hyperplasia with eosinophilia affecting the penis. Br J Dermatol. Sept 2008. 159(3):755-7. [QxMD MEDLINE Link]. ...
... Di Vitantonio, Hambra;De Paulis, Danilo;Ricci, ... Background: The angiolymphoid hyperplasia with eosinophilia (ALHE) is a sporadic vasoproliferative lesion of uncertain etiology ... Background: The angiolymphoid hyperplasia with eosinophilia (ALHE) is a sporadic vasoproliferative lesion of uncertain etiology ... Angiolymphoid hyperplasia with eosinophilia and entrapment of the ulnar nerve.pdf accesso aperto ...
Angiolymphoid Hyperplasia With Eosinophilia. p. 49. Sujay Khandpur, Neena Khanna. A case of angioymphoid hyperplasia with ... eosinophilia presenting as multiple scalp nodules closely mimicking benign appendageal tumour is reported. All the lesions were ...
Angiolymphoid hyperplasia with eosinophilia along with arteriovenous malformation: an unusual case. Year: 2022, Volume: 88, ...
Epithelioid haemangioma (also called angiolymphoid hyperplasia with eosinophilia, inflammatory angiomatous nodule, or atypical ... Intravascular papillary endothelial hyperplasia (IPEH), also called Massons tumour, is a benign, reactive, vascular ... Secondary intravascular papillary endothelial hyperplasia in a 45-year-old woman taking the aspect of a low-flow vascular ... Kim OH, Kim YM, Choo HJ et al (2016) Subcutaneous intravascular papillary endothelial hyperplasia: ultrasound features and ...
... papules and nodules mimicking angiolymphoid hyperplasia with eosinophilia, and lymphoma-like presentations with striking ... Up to about half of all patients are considered atopic, displaying a mild eosinophilia and/or elevated IgE. The histopathology ...
... see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA 1984-2020. History Note:. 2021; use ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA ... Unlike ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA it involves eosinophil infiltrates in lymph node and salivary glands and ... Unlike ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA it involves eosinophil infiltrates in lymph node and salivary glands and ... Angiolymphoid Hyperplasia with Eosinophilia [C15.378.553.231.085] Angiolymphoid Hyperplasia with Eosinophilia * Eosinophilia- ...
Angiolymphoid Hyperplasia with Eosinophilia Successfully Treated with Cryotherapy Nina Caca-Biljanovska, Irina Arsovska- ...
Absence of human polyomaviruses in angiolymphoid hyperplasia with eosinophilia in the United States. Lee, E. E., Sinkre, R., ...
Kimuras disease: involvement of regional lymph nodes and distinction from angiolymphoid hyperplasia with eosinophilia. Author( ... Kimuras disease: a clinico-pathological study of 21 cases and its distinction from angiolymphoid hyperplasia with eosinophils ... Increase of serum IgE with frequent localization of IgE in the germinal centres, mast cell hyperplasia in lymph nodes and ...
Angiolymphoid hyperplasia with eosinophilia. Arch Pathol Lab Med. 2015 May. 139 (5):683-6. [QxMD MEDLINE Link]. ... Reddy PK, Prasad AL, Sumathy TK, Shivaswamy KN, Ranganathan C. An Overlap of Angiolymphoid Hyperplasia with Eosinophilia and ... Ramchandani PL, Sabesan T, Hussein K. Angiolymphoid hyperplasia with eosinophilia masquerading as Kimura disease. Br J Oral ... Kimuras disease: a clinico-pathological study of 21 cases and its distinction from angiolymphoid hyperplasia with eosinophilia ...
Angiolymphoid hyperplasia with eosinophilia (disorder). Code System Preferred Concept Name. Angiolymphoid hyperplasia with ...
Thymus HyperplasiaFocal Nodular HyperplasiaFocal Epithelial HyperplasiaNeointimaAngiolymphoid Hyperplasia with Eosinophilia ... HyperplasiaProstatic HyperplasiaEndometrial HyperplasiaAdrenal Hyperplasia, CongenitalGingival HyperplasiaThymus Hyperplasia ... HyperplasiaProstatic HyperplasiaEndometrial HyperplasiaAdrenal Hyperplasia, CongenitalGingival Hyperplasia ... Focal Nodular HyperplasiaTunica IntimaFocal Epithelial HyperplasiaNeointimaAngiolymphoid Hyperplasia with EosinophiliaSteroid ...
keywords = "Angiolymphoid hyperplasia with eosinophilia, Epithelioid hemangioma, FOS, LMNA, VIM",. author = "Huang, {Shih ... The EHs were subclassified as typical (n=25), cellular (n=21), and angiolymphoid hyperplasia with eosinophilia (ALHE) (n=12) ... The EHs were subclassified as typical (n=25), cellular (n=21), and angiolymphoid hyperplasia with eosinophilia (ALHE) (n=12) ... The EHs were subclassified as typical (n=25), cellular (n=21), and angiolymphoid hyperplasia with eosinophilia (ALHE) (n=12) ...
Intra-arterial angiolymphoid hyperplasia with eosinophilia mimicking temporal arteritis: A case report and review of the ... Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign disease of unknown etiology, characterized by abnormal ...
Dilemma in diagnosing a post-auricular mass-angiolymphoid hyperplasia with eosinophilia versus Kimuras disease, an infrequent ...
Angiolymphoid Hyperplasia With Eosinophilia. * Cancers of the Oral Mucosa. * Cutaneous Squamous Cell Carcinoma ... Pilolli GP, Lucchese A, Scivetti M, Maiorano E, Favia G. Traumatic ulcerative granuloma with stromal eosinophilia of the oral ... Eleni G, Panagiotis S, Andreas K, Georgia A. Traumatic ulcerative granuloma with stromal eosinophilia: a lesion with alarming ... Marszałek A, Neska-Długosz I. Traumatic ulcerative granuloma with stromal eosinophilia. A case report and short literature ...
A Case of Angiolymphoid Hyperplasia with Eosinophilia Moon Joung Kim , So Yun Cho , Mi Ae Lee , Kyu Kwang Whang , Jeong Hee ...
ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA A RARE ENTITY. IMRAN A.A., ASHRAF A., RASHEED T., MUNIR S., TABISH S. AND SALEEM A ...
Angiolymphoid hyperplasia with eosinophilia on the palm. abstract::Angiolymphoid hyperplasia with eosinophilia (ALHE) is an ...
Olsen TG, Helwig EB: Angiolymphoid hyperplasia with eosinophilia. A clinicopathologic study of 116 patients. J Am Acad Dermatol ... Fetsch JF, Weiss SW: Observations concerning the pathogenesis of epithelioid hemangioma (angiolymphoid hyperplasia). Mod Pathol ... Clinical investigations include full blood count to exclude eosinophilia, ultrasound scan, color Doppler and MRI scans of the ... disease is characterized by multiple subcutaneous nodules and is associated with lymphadenopathy and blood eosinophilia. The ...
Angiolymphoid hyperplasia with eosinophilia treated with Mohs micrographic surgery. Trivedi, Apoorva; Norris, Ivy; DeWitt, ... The diagnosis of angiolymphoid hyperplasia with eosinophilia was confirmed. After discussing treatment modalities, the patient ...
VEGF-A Links Angiolymphoid Hyperplasia With Eosinophilia (ALHE) to THSD7A Membranous Nephropathy: A Report of 2 Cases. Am J ...
... a mimic of angiolymphoid hyperplasia with eosinophilia". Dermatology. 223 (4): 301-305. doi:10.1159/000335372. PMID 22269779. ... Angiolymphoid hyperplasia with eosinophilia,[47] cutaneous pseudolymphoma[48] Nerve. IgG4-related perineural disease[33][49]. ...
Case of Angiolymphoid Hyperplasia with Eosinophilia Associated with Anti-TNF Inhibitor. Neeraj Singh, Britta Sundquist and ... Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare, benign condition featuring nodular or papular lesions of the ...
Angiolymphoid hyperplasia with eosinophilia developing in a patient with history of peripheral T-cell lymphoma: evidence for ... Angiolymphoid hyperplasia with eosinophilia: evidence for a T-cell lymphoproliferative origin. Hum Pathol. 2002;33(10):1023- ... Morton K, Robertson AJ, Hadden W. Angiolymphoid hyperplasia with eosinophilia: report of a case arising from the radial artery ... juvenile temporal arteritis, angiolymphoid hyperplasia with eosinophilia, Kimura disease, temporal artery, temporal artery ...
Angiolymphoid Hyperplasia with Eosinophilia. *Breast Diseases. *Cutaneous Fistula. *Dermatitis. *Dermatomyositis. *Erythema. * ...
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon, vasoproliferative, idiopathic condition that manifests in adults as isolated or grouped papules, plaques, or nodules in the skin of the head and neck. (medscape.com)
  • Although angiolymphoid hyperplasia with eosinophilia (ALHE) may be a benign tumor, numerous factors suggest that it is an unusual reactive process. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is idiopathic. (medscape.com)
  • Background: The angiolymphoid hyperplasia with eosinophilia (ALHE) is a sporadic vasoproliferative lesion of uncertain etiology involving the skin and the subcutaneous tissue. (univaq.it)
  • The EHs were subclassified as typical (n=25), cellular (n=21), and angiolymphoid hyperplasia with eosinophilia (ALHE) (n=12) variants. (tmu.edu.tw)
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign disease of unknown etiology, characterized by abnormal vascular proliferation. (afsu.edu.tr)
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon dermal angioproliferating tumor, characterized by red to brown papules or nodules on the head and neck, though also occurring in the mouth, trunk, extremities and inguinal area. (shengsci.com)
  • Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare, benign condition featuring nodular or papular lesions of the dermis, subcutaneous tissue, and adjacent lymph nodes, commonly affecting the head and neck. (clinmedjournals.org)
  • The differential diagnosis consists of angiolymphoid hyperplasia with eosinophilia (ALHE) and Kimura disease. (najms.com)
  • Patients also typically have peripheral blood eosinophilia and elevated serum IgE. (medscape.com)
  • Approximately 20% of patients have blood eosinophilia. (medscape.com)
  • There was no associated blood eosinophilia, and the serum immunoglobulin E level was not obtained. (ajnr.org)
  • Increase of serum IgE with frequent localization of IgE in the germinal centres, mast cell hyperplasia in lymph nodes and changes of specific granules in the infiltrated eosinophils, such as roughness of the matrix and appearance of tubular structures together with fusing and disappearance of the core, were demonstrated in eosinophilic granuloma of the soft tissue, so-called Kimura's disease, in association with increase of anti-Candida IgE antibody. (indexindex.com)
  • The histopathologic features include intimal hyperplasia, endothelial hyperplasia, disruption of the internal elastic lamina and a lymphoeosinophilic panarteritis that lacks germinal centers and granulomatous inflammation. (najms.com)
  • Nearly all patients with Kimura disease demonstrate peripheral eosinophilia and elevated levels of serum IgE. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia developing in a patient with history of peripheral T-cell lymphoma: evidence for multicentric T-cell lymphoproliferative process. (najms.com)
  • Ramchandani PL, Sabesan T, Hussein K. Angiolymphoid hyperplasia with eosinophilia masquerading as Kimura disease. (medscape.com)
  • García Carretero R, Romero Brugera M, Rebollo-Aparicio N, Vazquez-Gomez O. Eosinophilia and multiple lymphadenopathy: Kimura disease, a rare, but benign condition. (medscape.com)
  • Kimura Y, Tsutsumi T, Kuroishikawa Y, Kishimoto S. Angiolymphoid hyperplasia with eosinophilia arising from the facial artery. (najms.com)
  • Angiolymphoid hyperplasia with eosinophilia (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory angiomatous nodule," "Intravenous atypical vascular proliferation," "Papular angioplasia," "Inflammatory arteriovenous hemangioma," and "Pseudopyogenic granuloma") usually presents with pink to red-brown, dome-shaped, dermal papules or nodules of the head or neck, especially about the ears and on the scalp. (wikipedia.org)
  • According to Takayama et al: "Dermatologists may be consulted to evaluate several seemingly disparate skin problems associated with IgG4-RD, which may include prurigo-like nodules, nonspecific, rosacea-like papules and pustules, scleroderma-like skin changes, xanthogranulomas, papules and nodules mimicking angiolymphoid hyperplasia with eosinophilia, and lymphoma-like presentations with striking swelling of secretory glands and lymph nodes, especially in the head and neck region. (aad.org)
  • A chronic inflammatory disease characterized by benign enlargement of cervical LYMPH NODE and SALIVARY GLANDS with increased levels of IMMUNOGLOBULIN E. Unlike ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA it involves eosinophil infiltrates in lymph node and salivary glands and mostly found in Asian males. (bvsalud.org)
  • Eleni G, Panagiotis S, Andreas K, Georgia A. Traumatic ulcerative granuloma with stromal eosinophilia: a lesion with alarming histopathologic presentation and benign clinical course. (medscape.com)
  • Follicular hyperplasia, marked eosinophilic infiltrate and eosinophilic abscesses, and the proliferation of postcapillary venules are characteristic histological findings. (medscape.com)
  • Pilolli GP, Lucchese A, Scivetti M, Maiorano E, Favia G. Traumatic ulcerative granuloma with stromal eosinophilia of the oral mucosa: histological and immunohistochemical analysis of three cases. (medscape.com)
  • Traumatic ulcerative granuloma with stromal eosinophilia (Riga-Fede's disease and traumatic eosinophilic granuloma). (medscape.com)
  • however, upon their withdrawal, the symptoms and esophageal eosinophilia recurred. (curehunter.com)
  • Up to about half of all patients are considered atopic, displaying a mild eosinophilia and/or elevated IgE. (aad.org)
  • Thymus hyperplasia is present in two thirds of all patients with myasthenia gravis. (lookformedical.com)
  • Reddy PK, Prasad AL, Sumathy TK, Shivaswamy KN, Ranganathan C. An Overlap of Angiolymphoid Hyperplasia with Eosinophilia and Kimura's Disease: Successful Treatment of Skin Lesions with Cryotherapy. (medscape.com)
  • It is unclear whether the epithelioid hemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to Kimura's disease (see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA). (uchicago.edu)
  • Tariq N, Sadiq S, Si K. Angiolymphoid Hyperplasia with Eosinophillia - A Rare Entity. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory angiomatous nodule," "Intravenous atypical vascular proliferation," "Papular angioplasia," "Inflammatory arteriovenous hemangioma," and "Pseudopyogenic granuloma") usually presents with pink to red-brown, dome-shaped, dermal papules or nodules of the head or neck, especially about the ears and on the scalp. (wikipedia.org)
  • 1. Categorization of cutaneous epithelioid angiomatous nodule as epithelioid hemangioma or angiolymphoid hyperplasia with eosinophilia: Clinicopathologic, immunohistochemical, and molecular analyses of seven lesions. (nih.gov)
  • 2. FOSB immunoreactivity in endothelia of epithelioid hemangioma (angiolymphoid hyperplasia with eosinophilia). (nih.gov)
  • 9. Epithelioid hemangioma (angiolymphoid hyperplasia with eosinophilia) in the oral mucosa. (nih.gov)
  • 12. Traumatic pseudoaneurysm: a possible early lesion in the spectrum of epithelioid hemangioma/angiolymphoid hyperplasia with eosinophilia. (nih.gov)
  • 13. Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma) of the external auditory canal, an unusual presentation in an adult female: a case report. (nih.gov)
  • 17. Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma) of the lung: a clinicopathologic and immunohistochemical study of two cases. (nih.gov)
  • In the recent years, epithelioid hemangioma was suggested as an alternate term for "angiolymphoid hyperplasia with eosinophilia" to emphasize the characteristic epithelioid or histiocytoid morphology of the proliferating endothelial cells and to reflect the belief that this was a benign process. (ijpmonline.org)
  • Epithelioid hemangioma (angiolymphoid hyperplasia with eosinophilia) arising on the extremities. (uchicago.edu)
  • Simultaneous presentation of Kimura disease and angiolymphoid hyperplasia with eosinophilia. (medscape.com)
  • Chan JK, Hui PK, Ng CS, Yuen NW, Kung IT, Gwi E. Epithelioid haemangioma (angiolymphoid hyperplasia with eosinophilia) and Kimura's disease in Chinese. (medscape.com)
  • Googe PB, Harris NL, Mihm MC Jr. Kimura's disease and angiolymphoid hyperplasia with eosinophilia: two distinct histopathological entities. (medscape.com)
  • One patient with Kimura's disease and angiolymphoid hyperplasia with eosinophilia also suffers from kidney injury]. (medscape.com)
  • 11. Angiolymphoid hyperplasia with eosinophilia and vascular tumors of the head and neck. (nih.gov)
  • The major physical manifestation of this disorder is slowly enlarging subcutaneous tumors characterized by the presence of eosinophilic lymphoid hyperplasia [1]. (ncku.edu.tw)
  • The prominent feature of lymphoid tissue was germinal center hyperplasia surrounded by several lobules associated with hyperplastic vascular structures. (researchsquare.com)
  • Huang M, Lloyd WC 3rd, O'Hara M. Angiolymphoid hyperplasia with eosinophilia: an unusual presentation in a child. (medscape.com)
  • Severe atherosclerosis of the aorta and development of peripheral T-cell lymphoma in an adolescent with angiolymphoid hyperplasia with eosinophilia. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia developing in a patient with history of peripheral T-cell lymphoma: evidence for multicentric T-cell lymphoproliferative process. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia affecting the scrotum: a rare case report with molecular evidence of T-cell clonality. (medscape.com)
  • Angiolymphoid hyperplasia with eosinophilia associated with pregnancy: a case report and review of the literature. (medscape.com)