Asakura Takanori, Ishii Makoto, Haraguchi Mizuha, Kamiyama Ikuo, Kohno Mitsutomo, Sakamaki Hiroyuki, Emoto Katsura, Hayashi Yuichiro, Sugiura Hiroaki, Kawada Ichiro, Soejima Kenzo, Namkoong Ho, Tasaka Sadatomo, Hasegawa Naoki, Betsuyaku Tomoko
Division of Pulmonary Medicine, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan.
Department of Medicine, Nippon Kokan Hospital, 1-2-1 Kokan-dori, Kawasaki, Kanagawa, 210-0852, Japan.
J Med Case Rep. 2015 Oct 26;9:238. doi: 10.1186/s13256-015-0723-4.
Mycobacterium avium complex (MAC) lung disease presenting as a solitary pulmonary nodule (MAC-SPN) is often asymptomatic, is more common in middle to old age, and mimics lung cancer or tuberculoma. We report herein a case of MAC-SPN in an immunocompetent young adult patient, presenting with persistent chest pain and a subacutely progressive nodule with high intense (18)F-fluorodeoxyglucose uptake. Histological examination of resected specimens revealed pleurisy, which is a rare finding of MAC-SPN.
A 36-year-old Japanese male presented with chest pain and a subacutely progressive pulmonary nodule. Positron emission tomography-computed tomography showed high intense (18)F-fluorodeoxyglucose uptake in the nodule. Owing to his continuous chest pain and subacutely progressive nodules, wedge resection was performed using video-assisted thoracoscopic surgery. Histological examination revealed an epithelioid granuloma and pleurisy, and the lung tissue culture was positive for mycobacteria identified as M. avium.
This is the first report of MAC-SPN occurring with persistent chest pain, suggesting that MAC should be considered in the differential diagnosis of a solitary pulmonary nodule, even for patients who experience persistent chest pain. As in the present case, surgical resection with video-assisted thoracoscopic surgery is a reasonable approach to the diagnosis and treatment of MAC-SPN with possible malignancy, especially as MAC can be diagnosed using resected lung tissue culture with histological confirmation.
鸟分枝杆菌复合群(MAC)肺病表现为孤立性肺结节(MAC-SPN)时通常无症状,在中老年人群中更为常见,且易与肺癌或结核瘤相混淆。我们在此报告一例免疫功能正常的年轻成年患者发生MAC-SPN的病例,该患者表现为持续性胸痛以及一个具有高(18)F-氟脱氧葡萄糖摄取的亚急性进展性结节。切除标本的组织学检查显示有胸膜炎,这在MAC-SPN中是一种罕见的发现。
一名36岁的日本男性出现胸痛和一个亚急性进展性肺结节。正电子发射断层扫描-计算机断层扫描显示该结节有高(18)F-氟脱氧葡萄糖摄取。由于其持续胸痛和亚急性进展性结节,采用电视辅助胸腔镜手术进行了楔形切除术。组织学检查显示为上皮样肉芽肿和胸膜炎,肺组织培养分枝杆菌阳性,鉴定为鸟分枝杆菌。
这是首例伴有持续性胸痛的MAC-SPN报告,提示即使对于出现持续性胸痛的患者,在孤立性肺结节的鉴别诊断中也应考虑MAC。如本病例所示,对于可能具有恶性的MAC-SPN,采用电视辅助胸腔镜手术进行手术切除是一种合理的诊断和治疗方法,特别是因为MAC可通过切除的肺组织培养并经组织学证实来诊断。