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合并性肠腺瘤/微小类癌

Combined Intestinal Adenomas/Microcarcinoids.

作者信息

Tamura Hiromi, Ando Hiroka, Doi Reiko, Adachi Shiro

机构信息

Department of Pathology, Toyonaka Municipal Hospital, Toyonaka, Japan.

出版信息

Case Rep Gastroenterol. 2019 Sep 27;13(3):410-417. doi: 10.1159/000503169. eCollection 2019 Sep-Dec.

Abstract

The combined colonic adenoma/microcarcinoid tumor is a rare intestinal neoplasm featuring intermingled adenomatous and carcinoid components. A few case reports and small case series have suggested that this entity exhibits an indolent clinical course. Here, we report two cases with these tumors, and describe the morphological features and clinical follow-up. A 61-year-old male and 78-year-old male presented with heme-positive stools at their medical checkups. Colonoscopy revealed masses in the colons; we performed endoscopic mucosal resection. Both lesions featured low-grade adenomas and low-grade neuroendocrine tumors. We diagnosed combined colonic adenomas/microcarcinoids. The clinical courses of both patients were benign at follow-up at 2.5 and 6 years. Awareness of this rare colonic tumor should prevent potential diagnostic pitfalls and may help clarify the natural history of these tumors and their possible relationships with composite glandular/carcinoid tumors.

摘要

结肠腺瘤/微小类癌瘤是一种罕见的肠道肿瘤,其特征是腺瘤成分和类癌成分混合存在。少数病例报告和小病例系列研究表明,这种实体瘤具有惰性的临床病程。在此,我们报告两例患有这些肿瘤的病例,并描述其形态学特征和临床随访情况。一名61岁男性和一名78岁男性在体检时出现大便潜血阳性。结肠镜检查发现结肠有肿物;我们进行了内镜黏膜切除术。两个病变均表现为低级别腺瘤和低级别神经内分泌肿瘤。我们诊断为结肠腺瘤/微小类癌。两名患者在2.5年和6年的随访中临床病程均为良性。认识这种罕见的结肠肿瘤应可避免潜在的诊断陷阱,并可能有助于阐明这些肿瘤的自然病史及其与复合性腺瘤/类癌肿瘤的可能关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a0/11387879/60c7bff5aa69/crg-0013-0410-g01.jpg

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