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Endometrial stromal sarcoma of the sigmoid colon arising in endometriosis: a case report with a review of literatures.

机译:乙状结肠的子宫内膜间质肉瘤在子宫内膜异位症中的发生:一例报道并有文献复习。

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摘要

Most of malignant tumors arising in ovarian and extraovarian endometriosis are carcinomas. Mixed mullerian tumor and endometrial stromal sarcoma arising in intestinal endometriosis are rarely described, but its clinicopathologic features have not been well characterized. Here we report a case of endometrial stromal sarcoma of the sigmoid colon arising in endometriosis with a review of six additional cases of endometrial stromal sarcoma arising in intestinal endometriosis found in English literatures. The patients ranged in age from 36 to 64 yr. Presenting symptoms were pain, bloody diarrhea, and tenesmus. Some patients had a previous history of endometriosis. Most of the tumors arose in the rectosigmoid colon. The histologic features were the same as their uterine counterpart. No death of disease had been reported. This rare tumor should not be confused with gastrointestinal stromal tumor clinically and histologically.
机译:卵巢和卵巢外子宫内膜异位症引起的大多数恶性肿瘤是癌。很少有描述混合性苗勒氏瘤和子宫内膜异位症引起的子宫内膜间质肉瘤,但其临床病理特征尚未得到很好的表征。在这里,我们报告一例发生于子宫内膜异位症的乙状结肠子宫内膜间质肉瘤,并回顾了六例英国文献中发现的肠内膜异位症引起的子宫内膜间质肉瘤。患者的年龄为36至64岁。表现为疼痛,出血性腹泻和里急后重。一些患者以前有子宫内膜异位病史。大多数肿瘤出现在直肠乙状结肠。组织学特征与子宫对应物相同。没有疾病死亡的报道。这种罕见的肿瘤在临床上和组织学上都不应与胃肠道间质瘤混淆。

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