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Cutaneous immunopathology. The diagnostic use of direct and indirect immunofluorescence techniques in dermatologic disease
s.l; s.n; nov. 1979. 29 p. ilus, tab.
Non-conventional em En | SES-SP, SESSP-ILSLACERVO, SES-SP | ID: biblio-1240604
Biblioteca responsável: BR191.1
Localização: [{"text": "BR191.1", "_a": "01512/s"}]
RESUMO
Direct and indirect immunofluorescence tests performed on skin biopsy specimens and serum have enriched the diagnostic skills of the practicing pathologist. Specific patterns of immunoglobulin and complement deposition have clarified the diagnostic entities within the group of vesiculobullous diseases. The pemphigus group of diseases is characterized by antibodies, usually IgC directed against the intercellular substance of squamous epithelium. The pemphigoid group of bullous diseases is characterized by antibodies, usually IgC directed against the basement membrane zone. The basement membrane zone deposition of immunoglobulin or complement is linear and localized to the lamina lucida. In dermatitis herpetiformis, granular or speckled IgA deposition in the upper papillary dermis is characteristic; however, other patterns of deposition may occur. Abnormal microfibrillar bundles in the upper papillary dermis have recently been identified in patients with dermatitis herpetiformis. Immunofluorescence studies of patients with lupus erythematosus are important not only in diagnosis but also in prognosis. The diseased skin of lupus patients contains deposits of immunoglobulin, usually IgC or IgM at the basement membrane zone in more than 90 per cent of the cases. In discoid lupus eryhtematosus, clinically normal skin does not contain such deposits. However, in systemic lupus erythemaosus, normal sun exposed skin contains these deposits in approximately 80 per cent of the cases and normal nonsun exposed skin contains them in 50 per cent of the cases. Direct immunofluorescence of normal skin may demonstrate basement membrane zone and other autoimmune diseases with anti-DNA antibodies. The skin of psoriatic patients may demonstrate in vivo bound IgC within the stratum corneum. Similar circulating antistratum corneum antibodies are found in normal subjects; however, these antibodies do not appear to have access to epidermal blinding sites. Patients with lichen planus characteristically have large globular depositis of immunoglobulin and complement in the epidermis and dermis in diseased skin. Granular deposition of Ig M and IgC at the basement membrane zone in lichen planus may lead to confusion with lupus erythematosus. Deposition of immunoglobulin and complement is found in and about vessels in early lesions of cutaneous vasculitis. Negative findings in older lesions may be due to immune complex degradation and removal.Further information.
Assuntos
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Coleções: 06-national / BR Base de dados: SES-SP / SESSP-ILSLACERVO Assunto principal: Dermatopatias / Dermatopatias Infecciosas / Dermatopatias Vesiculobolhosas / Doenças do Colágeno / Vasculite Leucocitoclástica Cutânea / Dermatite Limite: Humans Idioma: En Ano de publicação: 1979 Tipo de documento: Non-conventional País de publicação: Estados Unidos
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Coleções: 06-national / BR Base de dados: SES-SP / SESSP-ILSLACERVO Assunto principal: Dermatopatias / Dermatopatias Infecciosas / Dermatopatias Vesiculobolhosas / Doenças do Colágeno / Vasculite Leucocitoclástica Cutânea / Dermatite Limite: Humans Idioma: En Ano de publicação: 1979 Tipo de documento: Non-conventional País de publicação: Estados Unidos