A hemophagocytic lymphohistiocytosis patient initiated with prominent liver dysfunction: a case report / 中国医学科学杂志(英文版)
Chinese Medical Sciences Journal
;
(4): 191-193, 2014.
Artigo
em Inglês
| WPRIM
| ID: wpr-242871
ABSTRACT
Hemophagocytic lymphohistiocytosis (HLH) is an aggressive and potentially fatal syndrome that results from inappropriate activation of lymphocytes and macrophages. It is characterized by fever, hepatosplenomegaly, cytopenias, hypertriglyceridemia, hypofibrinogenemia, and pathologic findings of hemo- phagocytosis in the bone marrow or other tissues. We report an adult HLH case admitted to hepatology department.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Prednisona
/
Usos Terapêuticos
/
Tratamento Farmacológico
/
Linfo-Histiocitose Hemofagocítica
/
Hepatopatias
/
Testes de Função Hepática
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Chinese Medical Sciences Journal
Ano de publicação:
2014
Tipo de documento:
Artigo
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