Secondary hemophagocytic lymphohistiocytosis related to hematopoietic tuberculosis

被引：1
|
作者：
Zemed, Naaima [1 ]
Khatib, Samia [1 ]
Oualil, Houda [1 ]
Bourkadi, Jamal-eddine [1 ]
机构：
[1] Moulay Youssef Hosp, Dept Resp Dis, Rabat, Morocco
来源：
EGYPTIAN JOURNAL OF CHEST DISEASES AND TUBERCULOSIS | 2016年 / 65卷 / 01期
关键词：
Hemophagocytic lymphohistiocytosis; Macrophage activation syndrome; Hematopoietic tuberculosis;
D O I：
10.1016/j.ejcdt.2015.12.013
中图分类号：
R56 [呼吸系及胸部疾病];
学科分类号：
摘要：
Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially a fatal disease. It is either primary or secondary and it is linked to various etiologies. Its therapeutic management is always difficult and not codified in the absence of large-scale controlled studies. We report a case of secondary HLH associated with hematopoietic tuberculosis in an immunocompetent adult. (C) 2015 The Egyptian Society of Chest Diseases and Tuberculosis. Production and hosting by Elsevier B.V.
引用
收藏
页码：365 / 367
页数：3
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