Suppr超能文献

自胃肠道间质瘤中c-Kit突变确立以来小网膜原发性平滑肌肉瘤的首例报道

First Account of Primary Leiomyosarcoma of the Lesser Omentum since Establishment of c-Kit Mutations in Gastrointestinal Stromal Tumors.

作者信息

Saijo Fumito, Sato Kaoru, Handa Tomoko, Narushima Yoichi, Matsumura Naoki, Iwama Noriyuki, Nakayama Fumie, Tokumura Hiromi

机构信息

Department of Surgery, Tohoku Rosai Hospital, 4-3-21, Dainohara, Aobaku, Sendai, Miyagi 981-8563, Japan.

Department of Gastroenterology, Tohoku Rosai Hospital, 4-3-21, Dainohara, Aobaku, Sendai, Miyagi 981-8563, Japan.

出版信息

Case Rep Surg. 2019 Nov 4;2019:2426092. doi: 10.1155/2019/2426092. eCollection 2019.

Abstract

BACKGROUND

Primary omental leiomyosarcoma is an extremely rare type of tumor. Leiomyosarcomas originating from the lesser omentum have not been reported since immunohistochemical staining for c-kit has been used for the diagnosis of mesenchymal abdominal tumors. They are yet to be reported since gastrointestinal stromal tumors were categorized. Here we reported a case of successful resection of a lesser omental leiomyosarcoma.

CASE PRESENTATION

A 71-year-old man underwent ultrasonography at the outpatient clinic through which an upper abdominal tumor was identified. Following computed tomography and endoscopy, a 4.5 cm submucosal tumor in the lesser curvature of the stomach was highly suspected. A laparoscopic partial resection of the stomach was performed. Histopathological examination revealed the tumor to be a leiomyosarcoma arising from the lesser omentum that did not invade the stomach. Immunohistochemical staining showed that the tumor was negative for CD34, c-kit, and S-100 and positive for desmin and -smooth muscle actin. No recurrence had been observed 1 year after surgery without adjuvant chemotherapy.

CONCLUSIONS

Primary lesser omental leiomyosarcoma, which is difficult to diagnose before surgery given the location of the primary tumor in the lesser omentum, has rarely been reported. Considering the high possibility of malignancy, close observation is essential.

摘要

背景

原发性大网膜平滑肌肉瘤是一种极为罕见的肿瘤类型。自从免疫组化染色用于诊断腹部间叶组织肿瘤以来,起源于小网膜的平滑肌肉瘤尚未见报道。自从胃肠道间质瘤被分类以来,此类病例仍未见报道。在此,我们报告了一例成功切除小网膜平滑肌肉瘤的病例。

病例介绍

一名71岁男性在门诊接受超声检查时发现上腹部有一个肿瘤。经过计算机断层扫描和内窥镜检查,高度怀疑胃小弯处有一个4.5厘米的黏膜下肿瘤。遂进行了腹腔镜下胃部分切除术。组织病理学检查显示,该肿瘤是起源于小网膜的平滑肌肉瘤,未侵犯胃。免疫组化染色显示,肿瘤CD34、c-kit和S-100呈阴性,结蛋白和α-平滑肌肌动蛋白呈阳性。术后1年未进行辅助化疗,未观察到复发。

结论

原发性小网膜平滑肌肉瘤因原发肿瘤位于小网膜,术前难以诊断,鲜有报道。鉴于其恶性可能性高,密切观察至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aaa/6875344/7064ade8a8b6/CRIS2019-2426092.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验