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.
Artículo
en Inglés
| 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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Prednisona
/
Usos Terapéuticos
/
Quimioterapia
/
Linfohistiocitosis Hemofagocítica
/
Hepatopatías
/
Pruebas de Función Hepática
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Chinese Medical Sciences Journal
Año:
2014
Tipo del documento:
Artículo
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