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1.
Am J Ophthalmol ; 140(2): 262-6, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16086948

RESUMO

PURPOSE: To present two cases of conjunctival lesions exhibiting the Splendore-Hoeppli phenomenon, each with different immunohistochemical findings. DESIGN: Interventional case reports. METHODS: Two young males with conjunctival lesions underwent biopsy. Demographic data and timing of biopsy were extracted from the charts. The biopsy specimens were formalin fixed and paraffin embedded for light microscopy. Immunohistochemical staining using the peroxidase method was carried out on each for IgG, IgM, IgA, the C3 component of complement, and eosinophilic major basic protein. MAIN OUTCOME MEASURES: Presence of positive or negative staining for the various antigens. RESULTS: Both biopsy specimens exhibited the Splendore-Hoeppli phenomenon, a morphologically unique process consisting of an amorphous, eosinophilic material surrounded by epithelioid histiocytes, multinucleated giant cells, lymphocytes, and eosinophils. Two staining patterns were seen. One revealed predominately immunoglobulin deposition, whereas the other revealed primarily eosinophilic major basic protein. This is the first instance we are aware of in which eosinophilic major basic protein was the predominate finding in an ocular specimen. CONCLUSION: The composition of Splendore-Hoeppli phenomenon material varies and may be related to various factors, including timing of biopsy and prior treatment.


Assuntos
Doenças da Túnica Conjuntiva/patologia , Granuloma Eosinófilo/patologia , Granuloma de Células Gigantes/patologia , Adulto , Biópsia , Criança , Complemento C3a/metabolismo , Doenças da Túnica Conjuntiva/metabolismo , Proteína Básica Maior de Eosinófilos/metabolismo , Granuloma Eosinófilo/metabolismo , Granuloma de Células Gigantes/metabolismo , Humanos , Técnicas Imunoenzimáticas , Imunoglobulinas/metabolismo , Masculino
2.
Am J Ophthalmol ; 140(5): 949-52, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16310490

RESUMO

PURPOSE: To report the cases of four patients with hepatitis C virus infection who experienced clinical features that are virtually identical to Vogt-Koyanagi-Harada disease (VKH). DESIGN: Retrospective observational case series. METHODS: Medical records of patients who were referred between January and December 2003 were reviewed for diagnosis and management of VKH and who also had chronic hepatitis C virus (HCV) infection. RESULTS: Four white patients had the clinical features of VKH. Three of the patients experienced intraocular inflammation while they were being treated for HCV infection with pegylated interferon alpha 2b and ribavirin. The intraocular inflammation responded to systemic corticosteroid treatment and to discontinuation of antiviral agents. CONCLUSION: Although the number of patients who were studied is limited, there appears to be an association between HCV infection that was treated with pegylated interferon alpha 2b and the development of VKH-like disease. Further studies are required to confirm such an association.


Assuntos
Hepatite C Crônica/complicações , Síndrome Uveomeningoencefálica/complicações , Adulto , Antivirais/uso terapêutico , Quimioterapia Combinada , Feminino , Angiofluoresceinografia , Hepatite C Crônica/diagnóstico , Hepatite C Crônica/tratamento farmacológico , Humanos , Interferon alfa-2 , Interferon-alfa/uso terapêutico , Masculino , Pessoa de Meia-Idade , Polietilenoglicóis , Proteínas Recombinantes , Estudos Retrospectivos , Ribavirina/uso terapêutico , Síndrome Uveomeningoencefálica/diagnóstico , Síndrome Uveomeningoencefálica/tratamento farmacológico
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