Polyserositis in a patient with acute paracoccidioidomycosis and hepatosplenic schistosomiasis

dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:27:01Z
dc.date.accessioned2022-10-05T16:40:48Z
dc.date.available2014-05-20T15:27:01Z
dc.date.available2022-10-05T16:40:48Z
dc.date.created2014-05-20T15:27:01Z
dc.date.issued1995-05-01
dc.identifierMycopathologia. Dordrecht: Kluwer Academic Publ, v. 130, n. 2, p. 75-78, 1995.
dc.identifier0301-486X
dc.identifierhttp://hdl.handle.net/11449/37077
dc.identifier10.1007/BF01103453
dc.identifierWOS:A1995RU23700004
dc.identifier0000-0002-8059-0826
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3908665
dc.description.abstractA 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.
dc.languageeng
dc.publisherKluwer Academic Publ
dc.relationMycopathologia
dc.relation1.476
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectIMMUNODEFICIENCY
dc.subjectP-BRASILIENSIS
dc.subjectPARACOCCIDIOIDOMYCOSIS
dc.subjectPOLYSEROSITIS
dc.subjectSCHISTOSOMIASIS
dc.titlePolyserositis in a patient with acute paracoccidioidomycosis and hepatosplenic schistosomiasis
dc.typeArtigo


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