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Solitary Granular Cell Tumor of Cecum: A Case Report

机译:盲肠孤立性颗粒细胞瘤:一例报告

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摘要

Granular cell tumor (GCT) was first described by Abrikossof in 1926. This tumor is a benign neoplasm of unclear histogenesis that is generally believed to be of nerve sheath origin. GCT is not common and most often affects the tongue, skin, and soft tissue, although it may occur anywhere in the body. Gastrointestinal tract involvement, and especially that of the colon, is very rare. This usually benign tumor appears as a submucosal nodule, measuring less than 2 cm in diameter and is often found incidentally during colorectal examinations. We describe the case of a 27-year-old man with a GCT in the cecum that was detected after a screening colonoscopy. Endoscopic examination revealed a yellowish submucosal tumor, 0.7 cm in diameter. An endoscopic mucosal polypectomy was done for histological confirmation and treatment.
机译:颗粒细胞瘤(GCT)最早是由Abrikossof于1926年描述的。该肿瘤是组织形成不清楚的良性肿瘤,通常被认为是神经鞘起源的。 GCT并不常见,尽管它可能发生在身体的任何地方,但它通常会影响舌头,皮肤和软组织。胃肠道受累,尤其是结肠受累非常少。这种通常为良性的肿瘤表现为粘膜下结节,直径小于2 cm,通常在结直肠检查时偶然发现。我们描述了一个27岁的盲肠GCT患者,该患者在结肠镜筛查后被发现。内镜检查发现粘膜下肿瘤为淡黄色,直径为0.7 cm。进行内窥镜黏膜息肉切除术以进行组织学确认和治疗。

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