Unusual Mesenchymal Tumors of the Lower Gastrointestinal Tract: When You Hear Hoofbeats in the Night, Do Not Forget the Zebras.

Marco Barella, Gianluca Lopez, Stefano Ferrero, Maurizio Vecchi, Paolo Cantù, Giorgio Alberto Croci, Francesca Boggio, Alessandro Del Gobbo
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Abstract

Introduction: Little information about clinical presentation of mesenchymal tumors of the lower gastrointestinal (GI) tract due to their extreme heterogeneity is available for clinical management. Usually, small solitary asymptomatic polyps are accidently found during a screening colonoscopy performed for hematochezia, abdominal pain, constipation, diarrhea, and bowel obstruction. In this case series, we illustrate our experience with mesenchymal tumors of the lower GI tract, which are a group of unusual and quite challenging lesions.

Case presentation: We retrospectively collected mesenchymal tumors of the lower GI tract in our institution (Fondazione IRCSS Ca' Granda - Ospedale Maggiore Policlinico di Milano) during the last 10 years. We reviewed the histological slides, and, when necessary, we performed immunohistochemical analyses to better characterize the tumors. A total of 99 cases were identified: 45 GISTs, 42 lipomas, 4 leiomyomas, 3 Kaposi sarcomas, 1 schwannoma, 1 ganglioneuroma, 1 hemangioma, 1 inflammatory fibroid polyp, and 1 challenging case of spindle cell melanoma. We focused on the most rare entities excluding therefore all GISTs and lipomas from re-evaluation.

Conclusion: Mesenchymal tumors of the lower GI tract represent a highly heterogeneous group of lesions encompassing GISTs, lipomas, smooth muscle tumors (leiomyoma and leiomyosarcoma), GI schwannomas, inflammatory fibroid polyps, solitary fibrous tumors, and other unusual spindle cell tumors. Immunohistochemistry and, in selected cases, molecular biology remain a useful tool which, in addition to a meticulous study of the morphology, helps the pathologist in the tangled jungle of differential diagnosis.

下胃肠道不寻常的间充质肿瘤:当你在夜间听到马蹄声时,不要忘记斑马。
导言:由于下胃肠道间充质肿瘤的异质性,目前关于其临床表现的信息很少,无法用于临床治疗。通常,小的孤立的无症状息肉是在进行结肠镜检查时意外发现的,这些检查包括便血、腹痛、便秘、腹泻和肠梗阻。在这个病例系列中,我们阐述了我们对下消化道间充质肿瘤的经验,这是一组不寻常的且相当具有挑战性的病变。病例介绍:我们回顾性收集了近10年来在我们的机构(米兰Ospedale Maggiore Policlinico di Milano)的下消化道间充质肿瘤。我们回顾了组织学切片,必要时,我们进行了免疫组织化学分析,以更好地表征肿瘤。共发现99例:谷氨酸间质瘤45例,脂肪瘤42例,平滑肌瘤4例,卡波西肉瘤3例,神经鞘瘤1例,神经节神经瘤1例,血管瘤1例,炎性肌瘤息肉1例,梭形细胞黑色素瘤1例。我们集中于最罕见的实体,因此排除了所有的gist和脂肪瘤重新评估。结论:下消化道间充质肿瘤是一组高度异质性的病变,包括胃肠道间充质瘤、脂肪瘤、平滑肌肿瘤(平滑肌瘤和平滑肌肉瘤)、胃肠道神经鞘瘤、炎性肌瘤息肉、孤立纤维瘤和其他不寻常的梭形细胞肿瘤。免疫组织化学和在特定情况下,分子生物学仍然是一种有用的工具,除了对形态学的细致研究外,还有助于病理学家在复杂的鉴别诊断丛林中进行诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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