Primary Liposarcoma of the Stomach: a Case Report and a Review of the Literature

• Published in: Japanese Journal of Clinical Oncology Vol. 28; no. 4; pp. 284 - 288
• Main Authors: Seki, Kunihiko, Hasegawa, Tadashi, Konegawa, Ryuji, Hizawa, Kazuo, Sano, Toshiaki
• Format: Report
• Language: English
• Published: Foundation for Promotion of Cancer Research 01.04.1998
• Subjects: CD34; immunohistochemistry; liposarcoma; stomach; ultrastructure
• ISSN: 0368-2811; 1465-3621
• DOI: 10.1093/jjco/28.4.284

Primary liposarcoma of the stomach is rare and only seven cases have been described in the English literature. Here we report the eighth case, which occurred in a 68-year-old woman who presented with repeated tarry stools and hematemesis. Endoscopic examination revealed a large ulcerated submucosal mass at the gastric angle. The patient was treated by total gastrectomy. On microscopic examination, the tumor showed the features of a well differentiated sclerosing liposarcoma. Immunohistochemically, many spindle to stellate tumor cells were diffusely positive for vimentin and CD34. Positivity for S-100 protein was found in the adipocytic component, including lipoblasts, in addition to some spindle-shaped tumor cells. On ultrastructural examination, the spindle to stellate cells had features characteristic of fibroblasts. No recurrence or metastasis was seen during 13 months. Liposarcoma of the stomach has to be considered in the differential diagnosis with other submucosal lesions, such as gastric lipoma and gastrointestinal stromal tumor.