一名镰状细胞病患者的鸟分枝杆菌复合群相关噬血细胞性淋巴组织细胞增生症：一种罕见的致命关联
Mycobacterium avium Complex-Associated Hemophagocytic Lymphohistiocytosis in a Sickle Cell Patient: An Unusual Fatal Association.
作者信息
Chamsi-Pasha Mohammed A R, Alraies M Chadi, Alraiyes Abdul Hamid, Hsi Eric D
机构信息
Department of Internal Medicine, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
出版信息
Case Rep Hematol. 2013;2013:291518. doi: 10.1155/2013/291518. Epub 2013 May 16.
Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome, characterized clinically by fever, splenomegaly, cytopenia, and high ferritin. Infectious causes have been associated with secondary HLH, with viruses being the most common. We report a case of Mycobacterium avium complex-associated HLH in a sickle cell anemia patient. To the best of our knowledge, this association has never been reported in sickle cell anemia.
噬血细胞性淋巴组织细胞增生症（HLH）是一种罕见的高炎症综合征，临床特征为发热、脾肿大、血细胞减少和铁蛋白升高。感染性病因与继发性HLH有关，其中病毒最为常见。我们报告了一例镰状细胞贫血患者发生鸟分枝杆菌复合体相关HLH的病例。据我们所知，这种关联在镰状细胞贫血中从未有过报道。
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