Fukunaga Masaharu, Nomura Kouich
Department of Pathology, The Jikei Daisan Hospital, The Jikei University School of Medicine, 4-11-1 Izumihoncho, Komaeshi, Tokyo 201-8601, Japan.
Pathol Res Pract. 2004;200(7-8):545-9. doi: 10.1016/j.prp.2004.05.005.
A case of an epithelioid variant of pleomorphic liposarcoma (PL) arising in the back of a 72-year old male is presented. The lesion was a well-circumscribed but unencapsulated, yellowish white mass measuring 11 x 10 x 9 cm in the subcutis and muscle. Histologically, the tumor consisted of three elements; an epithelioid cell element occupying about 50%, a lipogenic and mixed lipogenic and epithelioid cell element occupying 40%, and a malignant fibrous histiocytoma-like element. The lipogenic area was composed of uni- and multivacuolated pleomorphic lipoblasts. Immunohistochemically, the tumor was positive for vimentin, epithelial membrane antigen, and CD10. It was negative for desmin, alpha-smooth muscle actin, muscle actin, S-100 protein, and cytokeratins 8 and 18. The epithelioid variant of PL should be differentiated from metastatic renal cell carcinoma and adrenal cortical adenocarcinoma.
本文报告一例发生于一名72岁男性背部的多形性脂肪肉瘤(PL)上皮样变型病例。病变为一个边界清楚但无包膜的黄白色肿块,位于皮下和肌肉层,大小为11×10×9 cm。组织学上,肿瘤由三种成分组成:上皮样细胞成分约占50%,脂肪生成性及脂肪生成与上皮样细胞混合性成分占40%,以及恶性纤维组织细胞瘤样成分。脂肪生成区域由单泡和多泡的多形性脂肪母细胞组成。免疫组化显示,肿瘤波形蛋白、上皮膜抗原和CD10呈阳性。结蛋白、α-平滑肌肌动蛋白、肌动蛋白、S-100蛋白以及细胞角蛋白8和18呈阴性。PL的上皮样变型应与转移性肾细胞癌和肾上腺皮质腺癌相鉴别。