脓肿分枝杆菌亚种马氏杆菌感染的抗干扰素- γ自身抗体

Q3 Medicine
Marino Hirata , Takahiko Fukuchi , Hitoshi Sugawara , Ibuki Kurihara , Keishiro Sueda , Akira Ishi , Maya Takazawa , Yasuhiro Yamaguchi , Hisashi Oshiro , Takuro Sakagami
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引用次数: 0

摘要

近年来,有抗干扰素-γ (IFN-γ)自身抗体的成人中播散性非结核分枝杆菌(NTM)感染的报道有所增加,特别是在东南亚。患者没有先前的免疫缺陷和非特异性初始症状可能导致诊断延迟。诊断标准包括临床症状、影像学表现和器官标本培养;然而,文化并不总是积极的。肉芽肿形成是NTM感染的特征性病理,有助于诊断,这在免疫缺陷存在时没有观察到。病例报告:一名69岁日本女性,无免疫缺陷史,表现为肺结节、中性粒细胞性皮肤病和化脓性淋巴结炎。行支气管镜检查、支气管穿刺细胞学检查、超声引导下支气管穿刺、ct引导下肺活检、胸腔镜下淋巴结活检、右侧锁骨下淋巴结活检、皮肤活检、血培养。结果培养阴性,病理检查显示炎性细胞浸润,以巨噬细胞为主。脓肿分枝杆菌在左侧腹股沟淋巴结的开放活检中发现马塞利斯氏菌。此外,商业化的IFN-γ释放试验QuantiFERON®TB Gold Plus尚无定论,而抗IFN-γ自身抗体呈阳性。值得注意的是,在症状出现8个月后,患者被诊断为弥散性脓肿分枝杆菌。由于存在抗ifn -γ自身抗体,马尾蚴感染与成人发病免疫缺陷相关。结论:由于抗ifn -γ自身抗体的识别延迟,缺乏阳性培养,没有肉芽肿形成,获得这一明确的诊断具有挑战性。因此,对于早期诊断,推荐使用QuantiFERON®TB Gold Plus筛选抗ifn -γ自身抗体,重复培养检查和病理研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mycobacterium abscessus subspecies massiliense infection with anti-interferon-gamma autoantibodies

Background

In recent years, reports of disseminated nontuberculous mycobacterial (NTM) infections in adults with anti-interferon-gamma (IFN-γ) autoantibodies have increased, particularly in Southeast Asia. The absence of previous immunodeficiency and nonspecific initial symptoms in patients are likely to cause a diagnostic delay. Clinical symptoms, imaging findings, and culture of organ specimens are included in the diagnostic criteria; however, the cultures are not always positive. Granuloma formation is a characteristic pathology of NTM infections, assisting in the diagnosis, which is not observed in the presence of immunodeficiency.

Case Report

A 69-year-old Japanese woman with no history of immunodeficiency presented with a pulmonary nodule, neutrophilic dermatosis, and pyogenic lymphadenitis. Bronchoscopy, transbronchial aspiration cytology, endobronchial ultrasound-guided transbronchial needle aspiration, computed tomography-guided lung biopsy, thoracoscopic lymph node biopsy, right subclavian lymph node biopsy, skin biopsy, and blood cultures were performed.

Results

While the cultures were negative, a pathological examination revealed inflammatory cell infiltrates, mainly composed of macrophages. Mycobacterium abscessus subsp. massiliense was recovered in an open biopsy of the left inguinal lymph node. Further, QuantiFERON®TB Gold Plus, a commercialized IFN-γ release assay, was inconclusive, whereas anti-IFN-γ autoantibodies were positive. Notably, eight months after symptom onset, the patient was diagnosed with disseminated M. abscessus subsp. massiliense infection associated with adult-onset immunodeficiency due to the presence of anti-IFN-γ autoantibodies.

Conclusion

Obtaining this definitive diagnosis was challenging owing to the delayed identification of anti-IFN-γ autoantibodies, a lack of positive cultures, and an absence of granuloma formation. Thus, for early diagnosis, screening for anti-IFN-γ autoantibodies using QuantiFERON®TB Gold Plus, repeated culture examinations, and pathological studies are recommended.

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来源期刊
Clinical Infection in Practice
Clinical Infection in Practice Medicine-Infectious Diseases
CiteScore
2.10
自引率
0.00%
发文量
95
审稿时长
82 days
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