肛门直肠平滑肌瘤:解剖形态不同的2例报告并文献复习。

Revista do Hospital das Clinicas Pub Date : 2004-10-01 Epub Date: 2004-10-29 DOI:10.1590/s0041-87812004000500013
Fábio Guilherme Campos, Andrea Furlan Leite, Sérgio Eduardo Alonso Araújo, Fábio César Atuí, Vítor Seid, Angelita Habr-Gama, Desidério Roberto Kiss, Joaquim Gama-Rodrigues
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引用次数: 21

摘要

胃肠道间充质肿瘤是一组罕见的胃肠道壁肿瘤,长期以来一直是混淆和争议的来源,特别是在病理分类、术前诊断、治疗策略和预后方面。本文报告2例直肠平滑肌瘤的临床表现及处理方法,并回顾相关文献。病例1:一名44岁的女性入院,报告在过去2年的右肛门旁区有一个结节。直肠检查发现,位于肛门旁区一个直径4厘米的纤维团块,在右直肠壁平滑肌下形成一个弓,位于肛门直肠环上方。腹部和骨盆的计算机断层扫描和磁共振成像显示病变,未发现其他异常。手术治疗包括通过肛门旁切口广泛局部切除肿瘤,不尝试进行淋巴结切除术。病例2:一名40岁男性患者入院,报告持续肛门疼痛4个月。他在直肠前壁齿状线上方有一个3厘米的粘膜下结节。术前2次不确定活检后,行经肛门肿瘤切除术。标本的组织学分析为良性平滑肌瘤。回顾文献提出,强调一些临床和治疗方面的这种不寻常的直肠肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anorectal leiomyomas: report of two cases with different anatomical patterns and literature review.

Gastrointestinal mesenchymal tumors comprise a rare group of gastrointestinal tract wall tumors that have long been a source of confusion and controversy, especially in terms of pathological classification, preoperative diagnosis, management strategies, and prognosis. This report describes the clinical manifestations and management of 2 rectal leiomyomas and reviews the pertinent literature. Case 1: A 44-year-old woman was admitted reporting a nodule in the right para-anal region for the previous 2 years. At proctological examination, a 4-cm diameter fibrous mass situated in the para-anal region that produced an arch under the smooth muscle on the right rectal wall just above the anorectal ring was noted. Computed tomography and magnetic resonance imaging of the abdomen and pelvis showed the lesion and detected no other abnormalities. Surgical treatment consisted of wide local resection of the tumor through a para-anal incision, with no attempts to perform lymphadenectomy. Case 2: A 40-year-old male patient was admitted reporting constant anal pain for 4 months. He presented a 3-cm submucosal nodule at the anterior rectal wall just above the dentate line. After 2 inconclusive preoperative biopsies, transanal resection of the tumor was performed. Histological analysis of the specimen showed a benign leiomyoma. A review of the literature is presented, emphasizing some clinical and therapeutic aspects of this unusual rectal tumor.

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