Yoshida R, Takada H, Iwamoto S, Uedono Y, Kawanishi H, Yoshioka K, Nakane Y, Hioki K, Sakaida N, Okamura A
Second Department of Surgery, Kansai Medical University, Osaka, Japan.
Surg Today. 1999;29(7):642-5. doi: 10.1007/BF02482992.
A case of a solitary fibrous tumor (SFT) of the perianal region in a 62-year-old man is reported herein. The patient had undergone an abdominoperineal excision of the rectum for an anorectal tumor 13 years previously, and had been referred to our hospital for a perineal mass. Computerized tomography and angiography revealed a markedly hypervascular tumor measuring 11 x 8 cm in size in the pelvic cavity. After preoperative radiotherapy (total 58 Gy) and the embolization of the feeding arteries, he underwent an en bloc excision of the tumor. Microscopically, the tumor was composed of spindle shaped cells with a "patternless" arrangement in a collagenous background. There was immunohistochemical evidence that these cells were strongly positive for CD34, thus suggesting the tumor to be SFT. The previously resected anorectal tumor showed similar histological and immunohistochemical findings. The patient's recovery was uneventful.
本文报道了一例62岁男性肛周区域孤立性纤维瘤(SFT)的病例。该患者13年前因肛肠肿瘤接受了腹会阴联合直肠切除术,此次因会阴肿物转诊至我院。计算机断层扫描和血管造影显示盆腔内有一个大小为11×8 cm的明显高血运肿瘤。在术前放疗(总量58 Gy)和对供血动脉进行栓塞后,他接受了肿瘤整块切除术。显微镜下,肿瘤由梭形细胞组成,在胶原背景中呈“无模式”排列。免疫组化证据表明这些细胞CD34呈强阳性,因此提示该肿瘤为SFT。先前切除的肛肠肿瘤显示出相似的组织学和免疫组化结果。患者恢复顺利。