Yamaguchi K, Soejima J, Maeda S, Kitamura K
Department of Surgery, Shinkokura Hospital, Kitakyushu, Japan.
Jpn J Surg. 1990 Jul;20(4):476-80. doi: 10.1007/BF02470836.
We report herein, a rare case of a 28 year old Japanese man with alveolar soft part sarcoma. The patient noticed a rapidly growing mass in the inner aspect of his left thigh and a smooth-surfaced, hard nodule revealing bruit on auscultation was found on physical examination. An angiogram showed dense neovascularity from the left profunda femoris artery. Histopathologically, the tumor was composed of nests of tumor cells with hyperchromatic nuclei and vesicular cytoplasm arranged in an alveolar fashion and a histopathologic diagnosis of alveolar soft part sarcoma was made. Immunohistochemically, the tumor cells had desmin and vimentin immunoreactants in the cytoplasm, suggesting muscle origin.
我们在此报告一例罕见的28岁日本男性肺泡软组织肉瘤病例。患者注意到左大腿内侧有一个迅速增大的肿块,体格检查发现一个表面光滑、质地坚硬的结节,听诊时有血管杂音。血管造影显示左股深动脉有密集的新生血管。组织病理学上,肿瘤由巢状肿瘤细胞组成,细胞核深染,细胞质呈空泡状,呈肺泡样排列,组织病理学诊断为肺泡软组织肉瘤。免疫组织化学检查显示,肿瘤细胞胞质中有结蛋白和波形蛋白免疫反应物,提示肿瘤起源于肌肉。