Portal hypertension secondary to Langerhans cell histiocytosis.
Artigo
em Inglês
| IMSEAR
| ID: sea-65646
ABSTRACT
We report two children, aged 2 and 2 1/2 years, with multisystem Langerhans cell histiocytosis (LCH). Both were administered chemotherapy, with apparently good response. However, hepatic fibrosis and portal hypertension were detected 5 and 1 1/2 years after therapy, respectively. The first child died after a bout of hematemesis. Hepatic fibrosis can proceed despite apparently successful chemotherapy in LCH.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Humanos
/
Masculino
/
Pré-Escolar
/
Histiocitose de Células de Langerhans
/
Diagnóstico Diferencial
/
Hipertensão Portal
Tipo de estudo:
Estudo diagnóstico
Idioma:
Inglês
Ano de publicação:
2001
Tipo de documento:
Artigo
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