Division of Thoracic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.
Surg Today. 2010 Nov;40(11):1073-8. doi: 10.1007/s00595-009-4203-6. Epub 2010 Nov 3.
Thymic basaloid carcinoma is an extremely rare tumor type, with only 10 such reports published to date in the English literature. We herein present a new case of thymic basaloid carcinoma with pleural dissemination that developed after a curative resection. A cystic tumor in the anterior mediastinum was observed in a 72-year-old man, and the tumor was completely resected via a median sternotomy with a combined resection of the adjacent structures. One year later, pleural disseminated nodules developed in the right thorax, which were resected through a right thoracotomy. The present case and the review of previous cases indicated that this rare tumor, which had previously been considered to be a low-grade malignant thymic carcinoma, may therefore have a more obstinate and aggressive malignant nature. Histopathologically, a few CD5-positive tumor cells were observed in isolation in the squamous epithelium of the inner cyst wall, thus suggesting that malignant transformation subsequently occurs in a preexisting cyst.
胸腺基底细胞癌是一种极其罕见的肿瘤类型,目前在英文文献中仅有 10 篇相关报道。本文报告了首例经根治性切除后发生胸膜播散的胸腺基底细胞癌。一名 72 岁男性因前纵隔囊性肿瘤就诊,经正中劈开胸骨入路完整切除肿瘤,同时联合切除毗邻结构。1 年后,患者右侧胸腔出现多发胸膜播散结节,行右侧开胸切除术。本病例及对以往病例的复习提示,这种罕见肿瘤此前被认为是低度恶性胸腺癌,可能具有更顽固和侵袭性的恶性生物学行为。组织病理学检查显示,囊壁内层的鳞状上皮中偶尔可见孤立的 CD5 阳性肿瘤细胞,提示恶性转化随后发生于预先存在的囊内。