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Eur J Pediatr ; 155(12): 1015-7, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8956935

RESUMO

UNLABELLED: We describe the case history of a 13-year-old girl with chronic fatigue and prolonged microcytic anaemia. She received oral iron since the age of 11 but failed to respond to it. Laboratory studies revealed elevated C-reactive protein and hypergammaglobulinaemia. A large solitary mesenterial lymph node could be demonstrated by ultrasonography and CT. A diagnosis of Castleman disease was suspected and confirmed histologically. After surgical removal of the lymphoma the patient recovered completely. CONCLUSION: Castleman disease should be considered in cases of chronic fatigue, unexplained fever, microcytic anaemia and hypergammaglobulinaemia.


Assuntos
Anemia/etiologia , Hiperplasia do Linfonodo Gigante , Adolescente , Anemia/tratamento farmacológico , Hiperplasia do Linfonodo Gigante/diagnóstico , Hiperplasia do Linfonodo Gigante/fisiopatologia , Hiperplasia do Linfonodo Gigante/cirurgia , Feminino , Humanos , Ferro/uso terapêutico
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