{"title":"脓肿分枝杆菌亚种马氏杆菌感染的抗干扰素- γ自身抗体","authors":"Marino Hirata , Takahiko Fukuchi , Hitoshi Sugawara , Ibuki Kurihara , Keishiro Sueda , Akira Ishi , Maya Takazawa , Yasuhiro Yamaguchi , Hisashi Oshiro , Takuro Sakagami","doi":"10.1016/j.clinpr.2023.100333","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Case Report</h3><p>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.</p></div><div><h3>Results</h3><p>While the cultures were negative, a pathological examination revealed inflammatory cell infiltrates, mainly composed of macrophages. <em><u>Mycobacterium abscessus</u></em> subsp. <em><u>massiliense</u></em> 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 <em><u>M. abscessus</u></em> subsp. <em><u>massiliense</u></em> infection associated with adult-onset immunodeficiency due to the presence of anti-IFN-γ autoantibodies.</p></div><div><h3>Conclusion</h3><p>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.</p></div>","PeriodicalId":33837,"journal":{"name":"Clinical Infection in Practice","volume":"21 ","pages":"Article 100333"},"PeriodicalIF":0.0000,"publicationDate":"2023-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590170223001164/pdfft?md5=5efd7cfa0bba482cc82d255010182eb2&pid=1-s2.0-S2590170223001164-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Mycobacterium abscessus subspecies massiliense infection with anti-interferon-gamma autoantibodies\",\"authors\":\"Marino Hirata , Takahiko Fukuchi , Hitoshi Sugawara , Ibuki Kurihara , Keishiro Sueda , Akira Ishi , Maya Takazawa , Yasuhiro Yamaguchi , Hisashi Oshiro , Takuro Sakagami\",\"doi\":\"10.1016/j.clinpr.2023.100333\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>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.</p></div><div><h3>Case Report</h3><p>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.</p></div><div><h3>Results</h3><p>While the cultures were negative, a pathological examination revealed inflammatory cell infiltrates, mainly composed of macrophages. <em><u>Mycobacterium abscessus</u></em> subsp. <em><u>massiliense</u></em> 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 <em><u>M. abscessus</u></em> subsp. <em><u>massiliense</u></em> infection associated with adult-onset immunodeficiency due to the presence of anti-IFN-γ autoantibodies.</p></div><div><h3>Conclusion</h3><p>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.</p></div>\",\"PeriodicalId\":33837,\"journal\":{\"name\":\"Clinical Infection in Practice\",\"volume\":\"21 \",\"pages\":\"Article 100333\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2590170223001164/pdfft?md5=5efd7cfa0bba482cc82d255010182eb2&pid=1-s2.0-S2590170223001164-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Infection in Practice\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590170223001164\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Infection in Practice","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590170223001164","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
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.