Small-Cell Lung Cancer Comorbid with Pulmonary <b><i>Mycobacterium avium</i></b> Infection: A Case Report

分枝杆菌复合群 肺癌 分枝杆菌 医学 微生物学 肺部感染 肺部感染 癌症研究 B细胞 生物 内科学 免疫学 病理 肺结核 抗体
作者
Masahiro Yamasaki,Kunihiko Funaishi,Naomi Saito,Kenichi Sakamoto,Sayaka Ishiyama,Kazuma Kawamoto,Yu Matsumoto,Naoko Matsumoto,Masaya Taniwaki,Nobuyuki Ohashi,Noboru Hattori
出处
期刊:Chemotherapy [S. Karger AG]
卷期号:63 (5): 257-261 被引量:1
标识
DOI:10.1159/000494504
摘要

Small-cell lung cancer (SCLC) rarely coexists with pulmonary Mycobacterium avium intracellular complex (MAC) infection. The key drug for SCLC treatment is etoposide, which is metabolized by cytochrome P-450 (CYP) 3A4. Meanwhile, the key drugs for pulmonary MAC infection are clarithromycin (CAM) and rifampicin (RFP), and their metabolism influences CYP3A4. Therefore, treatment of concurrent SCLC and pulmonary MAC infection is difficult, and to the best of our knowledge, no report of treatments for concurrent SCLC and pulmonary MAC infection has been published. Patient Concerns and Diagnoses: A 65-year-old man presented to our hospital with abnormal findings of chest computed tomography: (1) a hilar region nodule in the left lung and mediastinal lymphadenopathy and (2) a thick-walled cavity lesion in the right upper lobe of the lung. After further examinations, the former lesions were diagnosed as SCLC, cT4N3M0, stage IIIC and the latter as pulmonary MAC infection, fibrocavitary disease.Concurrent treatment was conducted with discontinuation of CAM and RFP before and after etoposide administration. Specifically, intravenous cisplatin and etoposide were administered on day 1 and days 1-3, respectively, and CAM, RFP, and ethambutol (EB) were administered orally on days 6-22 every 4 weeks. Concurrent radiotherapy was added to the drug administration on days 1-27 of the first cycle. The chemotherapy was continued for 4 cycles, followed by continuation of CAM and RFP administration. EB was discontinued because of optic nerve disorder. The treatments were conducted completely and safely, and both of the SCLC lesions and the MAC lesion were improved.Treatments for concurrent SCLC and pulmonary MAC infection may be successfully conducted with discontinuation of CAM and RFP before and after etoposide administration.

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