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胃神经鞘瘤伴巨大溃疡和淋巴结病,酷似胃癌:一例报告。

Gastric schwannoma with giant ulcer and lymphadenopathy mimicking gastric cancer: a case report.

机构信息

Department of Nuclear Medicine, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, 519000, China.

Department of pathology, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, 519000, China.

出版信息

BMC Gastroenterol. 2020 Feb 14;20(1):36. doi: 10.1186/s12876-020-01186-2.

Abstract

BACKGROUND

Gastric schwannomas are rare benign tumors originating from the intramuscular plexus of the stomach and account for just 2.6% of gastric mesenchymal tumors. Gastric schwannoma (GS) with a surface ulcer is very rare. Herein, we report a rare case of an ulcer-bearing GS, which in conjunction with multiple enlarged regional lymph nodes, readily mimicked gastric cancer (GC).

CASE PRESENTATION

A 79-year-old female presented with poor appetite and intermittent vomiting of gastric contents during the past month. Gastroscopy revealed a giant crateriform ulcer within the stomach body (at the angular notch). Its raised and indurated border was fragile and bled easily. GC was thus suspected. Contrast-enhanced computer tomography (CT) revealed a mild enhancement of the corresponding irregularly thickened gastric wall, and an annular zone of mucosal discontinuity. Enlarged regional lymph nodes were also found, making GC with metastases of lymph nodes our primary concern. F-fluorodeoxyglueose position emission tomography (F-FDG PET)/CT was then performed for further staging. Obviously increased FDG uptake was shown in the gastric lesion ((maximum standardized uptake value (SUV) 14.6), but no FDG uptake was observed in the enlarged regional lymph nodes. Given the strong suspicion of GC, subtotal gastrectomy was performed. GS was revealed by postoperative pathology, with no evidence of metastasis in the 13 resected lymph nodes.

CONCLUSIONS

This was a rare case of GS with a giant surface ulcer and multiple enlarged regional lymph nodes. The uptake of F-FDG in the tumor was substantially higher than previously published literature reports. Under these circumstances, it is difficult to be differentiated from GC.

摘要

背景

胃 schwannomas 是起源于胃的肌间丛的罕见良性肿瘤,仅占胃间质肿瘤的 2.6%。表面溃疡的胃 schwannoma(GS)非常罕见。在此,我们报告一例罕见的伴多发局部肿大淋巴结的溃疡型 GS,极易误诊为胃癌(GC)。

病例介绍

一名 79 岁女性因过去一个月食欲不振和间歇性呕胃内容物而就诊。胃镜检查显示胃体部(角切迹处)有一个巨大的火山口状溃疡。其隆起且变硬的边界脆弱且易出血。因此怀疑 GC。增强计算机断层扫描(CT)显示相应的不规则增厚胃壁轻度强化,环形黏膜连续性中断。还发现局部淋巴结肿大,使我们首先考虑 GC 伴淋巴结转移。然后进行 F-氟脱氧葡萄糖正电子发射断层扫描(F-FDG PET)/CT 进行进一步分期。胃病变处明显摄取 FDG(最大标准化摄取值(SUV)14.6),但肿大的局部淋巴结无 FDG 摄取。鉴于对 GC 的强烈怀疑,行胃次全切除术。术后病理显示为 GS,13 个切除淋巴结无转移证据。

结论

这是一例罕见的伴有巨大表面溃疡和多个局部肿大淋巴结的 GS 病例。肿瘤对 F-FDG 的摄取明显高于既往文献报道。在这种情况下,很难与 GC 区分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1843/7023701/b856fdc2a4ae/12876_2020_1186_Fig1_HTML.jpg

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