Moyana T N
Department of Pathology, University Hospital, Saskatoon, Saskatchewan, Canada.
Am J Gastroenterol. 1988 Jan;83(1):89-92.
Primary mesenteric liposarcomas (PMLs) are rare neoplasms, with a review of the English literature revealing only 10 cases. This paper describes an additional case of PML, and collates the currently documented cases, thus creating the framework for delineating the profile of this neoplasm. It is a tumor of adults that has characteristic clinicopathological and radiological features. In contradistinction from the retroperitoneal liposarcoma, the PML is eminently resectable, and requires aggressive surgical management.
原发性肠系膜脂肪肉瘤（PMLs）是一种罕见的肿瘤，回顾英文文献仅发现10例。本文描述了另外1例PML病例，并整理了目前已记录的病例，从而构建了描绘这种肿瘤特征的框架。它是一种成人肿瘤，具有特征性的临床病理和放射学特征。与腹膜后脂肪肉瘤不同，PML极易切除，需要积极的手术治疗。
