Mycobacterium abscessus subspecies massiliense infection with anti-interferon-gamma autoantibodies

医学 自身抗体 活检 病理 肉芽肿 非结核分枝杆菌 淋巴结活检 淋巴结 免疫缺陷 肺结核 免疫学 分枝杆菌 抗体 免疫系统
作者
Marino Hirata,Takahiko Fukuchi,Hitoshi Sugawara,Ibuki Kurihara,Keishiro Sueda,Akira Ishi,Maya Takazawa,Yasuhiro Yamaguchi,Hisashi Oshiro,Takuro Sakagami
出处
期刊:Clinical infection in practice [Elsevier BV]
卷期号:21: 100333-100333 被引量:1
标识
DOI:10.1016/j.clinpr.2023.100333
摘要

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, CT-guided lung biopsy, thoracoscopic lymph node biopsy, right subclavian lymph node biopsy, skin biopsy, and blood cultures were performed. 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. 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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