Ozeki Taichi, Higo Hisao, Omori Hiroki, Mori Shunta, Tanaka Shin, Makimoto Go, Ninomiya Kiichiro, Taniguchi Akihiko, Fujii Masanori, Miyoshi Kentaro, Rai Kammei, Ichihara Eiki, Ohashi Kadoaki, Sugimoto Seiichiro, Hotta Katsuyuki, Tabata Masahiro, Toyooka Shinichi, Maeda Yoshinobu, Miyahara Nobuaki
Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Japan.
Department of Allergy and Respiratory Medicine, Okayama University Hospital, Japan.
Intern Med. 2025 Apr 1;64(7):1093-1096. doi: 10.2169/internalmedicine.3854-24. Epub 2024 Sep 11.
A 55-year-old man presented to our hospital with idiopathic pulmonary fibrosis (IPF). He was registered with the Japan Organ Transplant Network the following year due to disease progression. Treatment with clarithromycin, ethambutol, and rifampicin for complications of Mycobacterium avium pulmonary disease was initiated, but sputum conversion could not be achieved. The administration of an amikacin liposome inhalation suspension (ALIS) resulted in sputum conversion, and single-lung transplantation was performed. ALIS therapy was continued after lung transplantation, and no M. avium disease was observed for 15 months. ALIS may cause M. avium pulmonary disease with additional indications for lung transplantation.
一名55岁男性因特发性肺纤维化(IPF)前来我院就诊。次年,由于疾病进展,他在日本器官移植网络进行了登记。开始使用克拉霉素、乙胺丁醇和利福平治疗鸟分枝杆菌肺病并发症,但痰菌转阴未成功。给予阿米卡星脂质体吸入混悬液(ALIS)后痰菌转阴,并进行了单肺移植。肺移植后继续进行ALIS治疗,15个月内未观察到鸟分枝杆菌病。ALIS可能导致鸟分枝杆菌肺病并增加肺移植的适应证。