Polyserositis in a patient with acute paracoccidioidomycosis and hepatosplenic schistosomiasis

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Data

1995-05-01

Autores

Shikanaiyasuda, M. A.
Benard, G.
Duarte, MIS
Leite, OHM
Eira, M.
Mendes-Giannini, Maria José Soares [UNESP]

Título da Revista

ISSN da Revista

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Editor

Kluwer Academic Publ

Resumo

A severe case of juvenile paracoccidioidomycosis (PCM), manifested as cholestatic jaundice, lymphnode enlargement and an unusual form of polyserositis, associated with portal hypertension secondary to schistosomiasis, as well as bacteremias caused by E. coli and S. aureus and post-transfusional hepatitis C is reported. Temporary unresponsiveness of in vivo and in vitro cellular immune responses to P. brasiliensis were registered. The authors discuss the possible interference of either agent in the host immune response, thus explaining the severity of PCM in the present case.

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Palavras-chave

IMMUNODEFICIENCY, P-BRASILIENSIS, PARACOCCIDIOIDOMYCOSIS, POLYSEROSITIS, SCHISTOSOMIASIS

Como citar

Mycopathologia. Dordrecht: Kluwer Academic Publ, v. 130, n. 2, p. 75-78, 1995.