首次报告一名慢性肉芽肿病患者感染了奇美拉分枝杆菌

Nancy E Aguilar Gómez , Uriel Pérez Blanco , Patricia Saltigeral Simental , Sara Espinosa Padilla , Jacinta Bustamante , Lizbeth Blancas Galicia
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引用次数: 0

摘要

慢性肉芽肿病(CGD)是一种先天性免疫错误。NADPH 氧化酶是一种产生各种活性氧(如超氧阴离子和过氧化氢)的酶复合物。CGD 中的分枝杆菌感染常见于这些微生物流行率较高的国家,如出生时接种卡介苗或结核病流行率较高的国家。非结核分枝杆菌(NTM)感染在CGD中很少见。患者还伴有嗜血细胞淋巴组织细胞增多症,使用丙种球蛋白和环孢素后症状缓解。在此,我们描述了首例由CYBA致病变体引起的常染色体隐性CGD女性患者感染M.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First report of Mycobacterium chimaera infection in a patient with chronic granulomatous disease

Chronic granulomatous disease (CGD) is an inborn error of immunity. NADPH oxidase is an enzyme complex that produces various reactive oxygen species, such as superoxide anions and hydrogen peroxide. Mycobacterial infections in CGD are commonly observed in countries with a high prevalence of these microorganisms, such as those receiving the BCG vaccination at birth or having a high prevalence of tuberculosis. Non-tuberculous mycobacteria (NTM) infections are rare in CGD. The patient also presented with hemophagocytic lymphohistiocytosis, which resolved with gammaglobulin and cyclosporine. Herein, we describe the first case of M. chimaera infection in a female patient with autosomal recessive CGD caused by a pathogenic variant in CYBA.

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