Kameda N, Kagesawa M, Hiruta N, Akima M, Ohki M, Matsumoto T
Acta Pathol Jpn. 1987 Feb;37(2):291-303.
A 62-year-old female with primary leiomyosarcoma of the left femur is reported with a review of 21 cases reported in the literature. The resected specimen showed that the tumor extended from the femoral head to the diaphysis for 13 cm in length. The tumor showed mainly intramedullary proliferation, but extraosseous growth was also noted at the great trochanter. Microscopic examination revealed well differentiated leiomyosarcoma characterized by interlacing bundles of fusiform cells with eosinophilic cytoplasm and rod-shaped hyperchromatic nuclei. PAP stain of actin on the tumor cells was positive. On electron microscopy, microfilament of 6-8 nm in diameter, dense bodies, pinocytotic vesicles, marginal attachment plate, and basal lamina were noted. The patient died with pulmonary metastasis, 1 year and 7 months after the operation. An autopsy showed metastases in the right pelvic cavity and bilateral lungs, and confirmed the primary site to be the left femur.
报告了一名62岁患有左股骨原发性平滑肌肉瘤的女性病例,并对文献报道的21例病例进行了回顾。切除的标本显示肿瘤从股骨头延伸至骨干,长度为13厘米。肿瘤主要表现为髓内增殖,但在大转子处也可见骨外生长。显微镜检查显示为高分化平滑肌肉瘤,其特征为交织成束的梭形细胞,胞质嗜酸性,核呈杆状深染。肿瘤细胞肌动蛋白的PAP染色呈阳性。电子显微镜检查发现直径为6 - 8纳米的微丝、致密体、吞饮小泡、边缘附着板和基膜。患者术后1年7个月死于肺转移。尸检显示右盆腔和双侧肺有转移,并证实原发部位为左股骨。