Wang Fang, Kiryu Shigeru, Li Li, Wang Qing, Li Dumin, Zhang Lifeng
Department of Radiology, Qi Lu Hospital of Shandong University, Jinan 250012, China.
Department of Radiology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
J Thorac Dis. 2017 Mar;9(3):E183-E187. doi: 10.21037/jtd.2017.03.29.
Primary pleural myxoid liposarcoma is a rare tumor. Here, we report a primary myxoid liposarcoma occupying the majority of the left thoracic cavity with features suggesting invasion. Computed tomography (CT) at medical check-up incidentally revealed a bulky inhomogeneous fatty mass. The tumor's large size made a prediction of its resectability by preoperative CT difficult. The patient underwent an operation, which revealed that the tumor was attached to the pleura with a thin pedicle; the tumor was resected completely. Few therapies for pleural liposarcoma other than resection are available; hence, surgery should be considered even if the tumor's size implies invasion on radiological imaging. In this case report, we discuss the imaging findings of this case with a review of the related literature.
原发性胸膜黏液样脂肪肉瘤是一种罕见的肿瘤。在此,我们报告一例原发性黏液样脂肪肉瘤占据左胸腔大部分区域且具有侵袭特征。体检时的计算机断层扫描(CT)偶然发现一个体积较大的不均匀脂肪性肿块。肿瘤体积较大使得术前通过CT预测其可切除性变得困难。患者接受了手术,术中发现肿瘤通过细蒂附着于胸膜;肿瘤被完整切除。除了手术切除外,针对胸膜脂肪肉瘤的治疗方法很少;因此,即使肿瘤大小在影像学上提示有侵袭,也应考虑手术治疗。在本病例报告中,我们结合相关文献复习讨论了该病例的影像学表现。