A primary leiomyosarcoma of small intestine: A rare case report

Gayatri Ajay Bamaniya, Krishna Kanubhai Patel, Cherry K Shah
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Abstract

Primary leiomyosarcoma of small intestine originating from smooth muscle cell is extremely rare entity. It mimics gastrointestinal stromal tumor (GIST) because of their common morphological appearance. Microscopic and immunochemistry findings are necessary to differentiate Leiomyosarcoma from gastrointestinal tumor (GIST). We report a case of 58-year-old male patient presented to tertiary care hospital with complain of generalized abdominal pain, vomiting, early satiety and constipation. Physical examination revealed no significant findings. Imaging findings showed Ileo-Ileal intussusceptions. Neither CT scan nor MRI reveal any evidence of tumor. The patient underwent exploratory laparotomy which revealed polypoidal mass in ileum. Resection and anastomosis of distal Ileum done & specimen received in histopathology department. On microscopic examination, Diagnosis of GIST & Leiomyosarcoma was considered. Immunohistochemistry was positive for Desmin marker and negative for CD 117, DOG 1, S-100 & ALK marker. The diagnosis of High grade Leiomyosarcoma was confirmed.
小肠原发性亮肌肉瘤:罕见病例报告
小肠原发性平滑肌肉瘤是一种极为罕见的肿瘤。它与胃肠道间质瘤(GIST)的形态外观相似。显微镜和免疫化学检查结果是鉴别雷米肉瘤和胃肠道肿瘤(GIST)的必要条件。我们报告了一例因全身腹痛、呕吐、早饱和便秘而到三级医院就诊的 58 岁男性患者。体格检查无明显发现。影像学检查结果显示为回肠-回肠肠套叠。CT 扫描和磁共振成像均未发现任何肿瘤迹象。患者接受了剖腹探查术,发现回肠内有息肉样肿块。对远端回肠进行了切除和吻合,组织病理科收到了标本。经显微镜检查,考虑诊断为 GIST 和 Leiomyosarcoma。免疫组化结果显示 Desmin 标记阳性,CD 117、DOG 1、S-100 和 ALK 标记阴性。确诊为高级别横纹肌肉瘤。
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