结肠炎性肌成纤维细胞瘤。

Journal of the Korean Surgical Society Pub Date : 2012-01-01 Epub Date: 2011-12-27 DOI:10.4174/jkss.2012.82.1.45
Eun Young Kim, In Kyu Lee, Yoon Suk Lee, Naery Yang, Dong Jin Chung, Kwang-Il Yim, Jin Il Kim, Seung Taek Oh
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引用次数: 47

摘要

炎症性肌纤维母细胞瘤(IMT)是一种罕见的间充质实体瘤,常见于儿童和年轻人。在此,我们报告一例经腹腔镜前切除术病理证实的结肠IMT。男,35岁,排便后肛门出血2周。结肠镜检查显示:在降结肠中心有一肿块伴浅溃疡,边缘不规则,并伴有完整粘膜。计算机断层扫描显示降结肠内一清晰均匀的孤立性肿块。我们进行了腹腔镜前切除术。本病例经显微镜检查诊断为IMT。肿瘤呈梭形细胞增生排列在透明质内,伴慢性炎性细胞,主要由浆细胞和淋巴细胞组成。免疫组化结果显示,肿瘤细胞中平滑肌肌动蛋白、vimentin呈阳性,desmin、CD117 (c-kit)、间变性淋巴瘤激酶-1呈阴性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inflammatory myofibroblastic tumor in colon.

Inflammatory myofibroblastic tumor in colon.

Inflammatory myofibroblastic tumor in colon.

Inflammatory myofibroblastic tumor in colon.

Inflammatory myofibroblastic tumor (IMT) is an uncommon mesenchymal solid tumor commonly documented in children and young adults. Here, we report a case of IMT in colon confirmed pathologically after laparoscopic anterior resection. A 35-year-old man presented with anal bleeding after defecation for 2 weeks. Colonoscopy demonstrated a mass with shallow ulceration in the central area and irregular margin accompanied by intact mucosa in the descending colon. Computer tomography showed a well-demarcated and homogenous solitary mass in the descending colon. We performed laparoscopic anterior resection. This case was diagnosed as IMT after microscopic examination. The tumor was composed of a proliferation of spindle-shaped cells arranged in the hyaline material with chronic inflammatory cells, composed mainly of plasma cells and lymphocytes. Immunohistochemically, tumor cells were positive for smooth muscle actin, and vimentin, and negative for desmin, CD117 (c-kit), anaplastic lymphoma kinase-1.

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