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GATA2缺乏症中的纵隔及播散性堪萨斯分枝杆菌病

Mediastinal and Disseminated Mycobacterium kansasii Disease in GATA2 Deficiency.

作者信息

Lovell Jana P, Zerbe Christa S, Olivier Kenneth N, Claypool Reginald J, Frein Cathleen, Anderson Victoria L, Freeman Alexandra F, Holland Steven M

机构信息

1 Laboratory of Clinical Infectious Diseases, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, and.

2 Pulmonary Clinical Medicine Section, Cardiovascular and Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland; and.

出版信息

Ann Am Thorac Soc. 2016 Dec;13(12):2169-2173. doi: 10.1513/AnnalsATS.201603-207BC.

Abstract

RATIONALE

Mycobacterium kansasii usually causes chronic pulmonary infections in immunocompetent patients. In contrast, disseminated M. kansasii disease is commonly associated with advanced human immunodeficiency virus infection, but is reported infrequently in other immunocompromised patients.

OBJECTIVES

To identify common clinical manifestations and potential risk factors for M. kansasii infection in patients with GATA2 deficiency.

METHODS

We reviewed M. kansasii disease associated with GATA2 deficiency at one institution and disease associated with primary and other immunodeficiencies reported in the literature.

MEASUREMENTS AND MAIN RESULTS

Nine patients with GATA2 deficiency developed M. kansasii infections. Six patients developed disseminated disease. All patients presented with significant mediastinal lymphadenopathy or abscesses. Seven patients had pulmonary risk factors, including six smokers. The majority of patients had low numbers of neutrophils, monocytes, B cells, CD4 T cells, and natural killer cells. Other conditions associated with disseminated M. kansasii disease were thymic disorders and IFN-γ/IL-12 defects.

CONCLUSIONS

Disseminated M. kansasii disease involving mediastinal lymph nodes is surprisingly common in GATA2 deficiency, but also occurs in defects of IFN-γ synthesis and response. Disseminated M. kansasii should be considered a marker indicating a need to evaluate for immunodeficiency syndromes.

摘要

原理

堪萨斯分枝杆菌通常在免疫功能正常的患者中引起慢性肺部感染。相比之下,播散性堪萨斯分枝杆菌病通常与晚期人类免疫缺陷病毒感染相关,但在其他免疫功能低下的患者中报道较少。

目的

确定GATA2缺乏患者中堪萨斯分枝杆菌感染的常见临床表现和潜在危险因素。

方法

我们回顾了一家机构中与GATA2缺乏相关的堪萨斯分枝杆菌病以及文献中报道的与原发性和其他免疫缺陷相关的疾病。

测量指标和主要结果

9例GATA2缺乏患者发生了堪萨斯分枝杆菌感染。6例患者发生了播散性疾病。所有患者均出现明显的纵隔淋巴结肿大或脓肿。7例患者有肺部危险因素,其中6例为吸烟者。大多数患者的中性粒细胞、单核细胞、B细胞、CD4 T细胞和自然杀伤细胞数量较低。与播散性堪萨斯分枝杆菌病相关的其他情况包括胸腺疾病和IFN-γ/IL-12缺陷。

结论

在GATA2缺乏患者中,累及纵隔淋巴结的播散性堪萨斯分枝杆菌病出人意料地常见,但在IFN-γ合成和反应缺陷中也会发生。播散性堪萨斯分枝杆菌病应被视为一个标志,表明需要评估免疫缺陷综合征。

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