Haemophagocytic lymphohistiocytosis driven by disseminated Mycobacterium haemophilum infection.

Q3 Medicine
Skin health and disease Pub Date : 2025-02-26 eCollection Date: 2025-04-01 DOI:10.1093/skinhd/vzae020
Parissa Irom, Ivan Rodriguez, Paige Kingston, Yasmin Gutierrez, Scott Worswick
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引用次数: 0

Abstract

Mycobacterium haemophilum is a nontuberculous mycobacteria that primarily affects immunocompromised patients. It can lead to a wide variety of clinical manifestations including infections of the skin, soft tissue and joints. Due to the significant heterogeneity in clinical presentation and difficulty isolating the organism, diagnosis can be difficult and is often delayed. Our patient's course was further complicated by the development of haemophagocytic lymphohistiocytosis (HLH). Although M. tuberculosis infection is recognized as a potential association, HLH driven by a disseminated M. haemophilum infection has not yet been reported. Here we present a case of disseminated M. haemophilum infection in an immunocompromised patient who developed haemophagocytic lymphohistiocytosis.

由弥散性嗜血杆菌感染引起的嗜血球性淋巴组织细胞增多症。
血友病分枝杆菌是一种非结核分枝杆菌,主要影响免疫功能低下的患者。它可以导致各种各样的临床表现,包括皮肤、软组织和关节的感染。由于临床表现的显著异质性和难以分离的有机体,诊断可能是困难的,往往是延迟。我们的病人的过程是进一步复杂的发展嗜血性淋巴组织细胞病(HLH)。虽然结核分枝杆菌感染被认为是一种潜在的关联,但由弥散性嗜血杆菌感染驱动的HLH尚未有报道。在这里,我们提出一个病例播散性嗜血杆菌感染在免疫功能低下的病人谁发展嗜血细胞淋巴组织细胞增多症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
0.00%
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0
审稿时长
10 weeks
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