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Eur J Gastroenterol Hepatol ; 25(7): 869-74, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23510963

RESUMO

Rosai-Dorfman disease, formerly known as 'sinus histiocytosis with massive lymphadenopathy', is a rare self-limiting histiocytic proliferative disorder typically presenting early in life with cervical lymphadenopathy and nonspecific systemic symptoms. Although it is usually a nodal disease, extranodal lesions may be encountered in some cases. The gastrointestinal tract is uncommonly affected in Rosai-Dorfman disease and its diagnosis depends on clinical suspicion and careful histopathological examination of biopsy samples taken from involved gastrointestinal segments. Here, we report a case of atypical Rosai-Dorfman disease with systemic symptoms and diffuse gastrointestinal involvement that led to a diagnostic and therapeutic challenge.


Assuntos
Gastroenteropatias , Histiocitose Sinusal , Idoso , Biópsia , Quimioterapia Combinada , Endoscopia Gastrointestinal , Endossonografia , Evolução Fatal , Fármacos Gastrointestinais/uso terapêutico , Gastroenteropatias/diagnóstico , Gastroenteropatias/terapia , Neoplasias Gastrointestinais/diagnóstico , Histiocitose Sinusal/diagnóstico , Histiocitose Sinusal/terapia , Humanos , Imunossupressores/uso terapêutico , Masculino , Valor Preditivo dos Testes , Resultado do Tratamento
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