Fujimoto Keisuke, Kenzaki Koichiro, Kubo Takako, Sawada Toru, Norimura Shoko, Miura Kazumasa, Yamamoto Akiyoshi
Chest Medical Center, Takamatsu Red Cross Hospital, Takamatsu, Kagawa, Japan.
Ann Thorac Cardiovasc Surg. 2025;31(1). doi: 10.5761/atcs.cr.25-00082.
Thymomas are commonly associated with autoimmune diseases such as myasthenia gravis (MG), pure red cell aplasia, and hypogammaglobulinemia, while those associated solely with alopecia areata (AA) are extremely rare. A 55-year-old woman with AA underwent chest computed tomography, which revealed a 33-mm anterior mediastinal cystic mass with fluctuating size. She was referred to our department for evaluation of a suspected cystic thymoma. The patient underwent thoracoscopic tumor resection under general anesthesia with isolated lung ventilation in the left lateral decubitus position. The operation lasted 81 minutes with minimal blood loss, and her postoperative course was uneventful. Histopathology confirmed a type B2-dominant thymoma. Notably, the patient's AA improved rapidly after surgery and did not recur for at least 3 years. This case strongly suggests a potential immunological relationship between AA and thymoma, though further research is needed to confirm this relationship.
胸腺瘤通常与自身免疫性疾病相关,如重症肌无力(MG)、纯红细胞再生障碍性贫血和低丙种球蛋白血症,而仅与斑秃(AA)相关的胸腺瘤极为罕见。一名患有斑秃的55岁女性接受了胸部计算机断层扫描,结果显示前纵隔有一个33毫米的囊性肿块,大小波动。她因疑似囊性胸腺瘤被转诊至我们科室进行评估。患者在全身麻醉下、左侧卧位单肺通气的情况下接受了胸腔镜肿瘤切除术。手术持续了81分钟,失血极少,术后恢复顺利。组织病理学证实为B2型为主的胸腺瘤。值得注意的是,患者的斑秃在手术后迅速改善,并且至少3年未复发。该病例强烈提示斑秃与胸腺瘤之间可能存在免疫关系,不过仍需进一步研究来证实这种关系。