| Literature DB >> 21046508 |
Noriaki Sakakura1, Hisashi Tateyama, Noriyasu Usami, Kohei Yokoi.
Abstract
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.Entities:
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Year: 2010 PMID: 21046508 DOI: 10.1007/s00595-009-4203-6
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549