Suppr超能文献

[胃神经鞘瘤:急性上消化道出血的罕见鉴别诊断]

[Gastric schwannoma: rare differenzial diagnosis of acute upper gastrointestinal (GI) bleeding].

作者信息

Lyros Orestis, Schickel Stephan, Schierle Katrin, Hoffmeister Albrecht, Gockel Ines

机构信息

Klinik für Viszeral-, Transplantations-, Thorax- und Gefäßchirurgie, Universitätsklinikum Leipzig, AöR, Germany.

Klinik für Innere Medizin, Muldentalkliniken GmbH, Krankenhaus Wurzen, Germany.

出版信息

Z Gastroenterol. 2017 Aug;55(8):761-765. doi: 10.1055/s-0042-114576. Epub 2017 Aug 10.

Abstract

Schwannomas are benign tumors derived from Schwann cells and their typical site of origin is the subcutaneous tissue of the extremities. Gastrointestinal localization of Schwannomas is extremely rare and the stomach is the prevalent site. Gastric schwannomas primarily occur in the gastric submucosa and are usually asymptomatic.We present a rare case of a solitary gastric schwannoma in a 51-year old male, which initially manifested with hematemesis by acute upper gastrointestinal (GI) bleeding. The upper GI-Endoscopy revealed a gastric submucosal tumor, 7 cm in size, located in the proximal corpus and fundus. In the endoscopical Ultrasound (EUS-Examination), the lesion appeared to arise from the fourth proper muscle layer (Muscularis propria). The fourth layer origin and the isoechogenicity, as compared to the normal muscle layer, are endoscopic ultrasonographic characteristics of gastric schwannomas and help in distinguishing them from gastrointestinal tumors (GIST). Because of the unclear histological identity, the patient underwent a "rendezvous" endoscopic-laparoscopic surgical resection of the tumor in toto. The histomorphological features of the lesion and the strong expression of S100 in combination with absence of DOG1 expression indicated the diagnosis of gastric schwannoma. There was no evidence of malignancy. The postoperative course was uncomplicated.This is a very rare manifestation of gastric schwannoma, representing a rare differenzial diagnosis in a case of acute upper GI-Bleeding. Only 14 % of gastric schwanommas are presented with gastrointestinal bleeding, including mainly melena rather than hematemesis. This case is considered to be worthy of presentation owing to the rare and unusual cause of upper GI bleeding implied in it.

摘要

施万细胞瘤是源自施万细胞的良性肿瘤,其典型起源部位是四肢的皮下组织。胃肠道施万细胞瘤极为罕见,胃部是其常见部位。胃施万细胞瘤主要发生于胃黏膜下层,通常无症状。我们报告一例罕见的51岁男性孤立性胃施万细胞瘤,最初表现为急性上消化道出血导致的呕血。上消化道内镜检查发现一个7厘米大小的胃黏膜下肿瘤,位于胃体近端和胃底。在内镜超声检查中,病变似乎起源于第四层固有肌层。与正常肌层相比,起源于第四层且等回声是胃施万细胞瘤的内镜超声特征,有助于将其与胃肠道肿瘤(胃肠道间质瘤)区分开来。由于组织学特征不明确,患者接受了肿瘤的“会师”内镜-腹腔镜全切除手术。病变的组织形态学特征以及S100的强表达且DOG1表达缺失提示胃施万细胞瘤的诊断。无恶性证据。术后病程顺利。这是胃施万细胞瘤非常罕见的表现,在急性上消化道出血病例中是一种罕见的鉴别诊断。只有14%的胃施万细胞瘤表现为胃肠道出血,主要包括黑便而非呕血。鉴于该病例中隐含的上消化道出血的罕见且不寻常原因,认为值得报告。

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