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Titolo:
ANGIOIMMUNOBLASTIC LYMPHADENOPATHY MIMICK ING DERMATITIS-HERPETIFORMIS (DUHRINGS-DISEASE)
Autore:
ZUMDICK M; MEGAHED M; BORCHARD F; WOHDE D; GOERZ G;
Indirizzi:
HEINRICH HEINE UNIV,HAUTKLIN,MOORENSTR 5 D-40225 DUSSELDORF GERMANY HEINRICHG HEINE UNIV,INST PATHOL DUSSELDORF GERMANY
Titolo Testata:
Hautarzt
fascicolo: 8, volume: 45, anno: 1994,
pagine: 562 - 565
SICI:
0017-8470(1994)45:8<562:ALMID>2.0.ZU;2-X
Fonte:
ISI
Lingua:
GER
Soggetto:
ANGIOIMMUNOBLASTIC LYMPHADENOPATHY; DYSPROTEINEMIA;
Keywords:
ANGIOIMMUNOBLASTIC LYMPHADENOPATHY; BULLOUS SKIN LESIONS; DERMATITIS-HERPETIFORMIS DUHRINGS DISEASE;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
17
Recensione:
Indirizzi per estratti:
Citazione:
M. Zumdick et al., "ANGIOIMMUNOBLASTIC LYMPHADENOPATHY MIMICK ING DERMATITIS-HERPETIFORMIS (DUHRINGS-DISEASE)", Hautarzt, 45(8), 1994, pp. 562-565

Abstract

A 62-year-old female patient presented with bullous, intensely itching cutaneous lesions, which clinically and histopathologically resembled dermatitis herpetiformis (Duhring's disease). Therapy with DADPS wasunsuccessful. Because of associated cervical lymph node enlargement and splenomegaly, a lymph node biopsy was taken. Histopathology of a lymph node and of the bone marrow confirmed the diagnosis: angioimmunoblastic lymphadenopathy (AILD)-type T-cell lymphoma. Intensely pruritic associated skin eruptions are typical for this peculiar kind of lymphoma. These skin lesions are due to inflammatory cells and not to neoplastic infiltrations. This case report is the first report of AILD with bullous skin lesions to appear in the literature.

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Documento generato il 03/12/20 alle ore 21:16:27