dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:19:47Z
dc.date.available2014-05-27T11:19:47Z
dc.date.created2014-05-27T11:19:47Z
dc.date.issued1999-11-01
dc.identifierRevista Brasileira de Medicina, v. 56, n. 11, p. 1147-1152, 1999.
dc.identifier0034-7264
dc.identifierhttp://hdl.handle.net/11449/65883
dc.identifier2-s2.0-5844321368
dc.identifier6309835137998766
dc.identifier4463138671998432
dc.identifier5016839015394547
dc.description.abstractCastleman's disease (CD) is an uncommon lymphoproliferative disorder that is morphologically and clinically heterogeneous. Both a localized benign variant and a multicentric form with systemic manifestations have been described. Although there are many published cases in literature, there are a few reports about this pathology in Brazil. We describe a patient with several manifestations of multicentric CD: lymphadenopathy, weight loss, fever, arthralgia, myalgia, and hepatosplenomegaly. Pathological examination of excised cervical lymph node revealed its rarest form: a CD of the hyaline-vascular type in multicentric presentation.
dc.languagepor
dc.relationRevista Brasileira de Medicina
dc.relation0,101
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectAngiofollicular lymph node hyperplasia
dc.subjectHepatosplenomegaly
dc.subjectLymphadenopathy
dc.titleDoença de Castleman multicêntrica: Relato de um caso
dc.typeArtículos de revistas


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