Haemophagocytic lymphohistiocytosis: an uncommon clinical presentation of tuberculosis

被引：0
|
作者：
Shea, Y. F. [1 ]
Chan, Jasper F. W. [2 ]
Kwok, W. C. [1 ]
Hwang, Y. Y. [1 ]
Chan, T. C. [1 ]
Ni, Michael Y. X. [1 ]
Li, Iris W. S. [2 ]
Chiu, Patrick K. C. [1 ]
Luk, James K. H. [1 ]
Chu, L. W. [1 ]
机构：
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Pokfulam, Hong Kong, Peoples R China
[2] Univ Hong Kong, Queen Mary Hosp, Dept Microbiol, Pokfulam, Hong Kong, Peoples R China
来源：
HONG KONG MEDICAL JOURNAL | 2012年 / 18卷 / 06期
关键词：
Lymphohistiocytosis; hemophagocytic; Tuberculosis; OF-THE-LITERATURE; MILIARY TUBERCULOSIS; HEMODIALYSIS-PATIENT; HISTIOCYTIC HEMOPHAGOCYTOSIS; ORGAN DYSFUNCTION; BONE-MARROW; PANCYTOPENIA; MYCOBACTEREMIA; FAILURE;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Secondary haemophagocytic lymphohistiocytosis is a rare but fatal complication of tuberculosis. We describe two cases, and review the local and international experience on the management of this clinical entity. Prompt treatment with anti-tuberculous drugs forms the cornerstone of therapeutic success.
引用
收藏
页码：517 / 525
页数：9
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