Gastric schwannoma: a case report.

IF 0.5 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2026-10-19 eCollection Date: 2026-10-01 DOI:10.1093/jscr/rjag927
Mohamed Tariq Haniff, Andrew Tse, Guillermo Becerril-Martinez
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引用次数: 0

Abstract

Gastric schwannomas are rare, benign mesenchymal tumours that closely mimic gastrointestinal stromal tumours (GISTs) on imaging, despite fundamentally different biological behaviour. We report a 74-year-old man with a background of proctocolectomy for rectal cancer, found incidentally to have a 5 cm exophytic gastric mass on surveillance gastroscopy. Endoscopic ultrasound-guided fine needle aspiration favoured schwannoma, and the patient underwent an uncomplicated laparoscopic gastric wedge resection. Histopathology confirmed gastric schwannoma with clear margins and no nodal involvement; immunohistochemistry was positive for S100 calcium-binding protein (S100)/SRY-box transcription factor 10 (SOX10) and negative for discovered on GIST-1 (DOG1)/CD117 (c-KIT)/smooth muscle actin (SMA)/desmin, excluding GIST. He recovered well and was discharged after 2 days, with a conservative surveillance endoscopy plan (6 months, then annually for 5 years) agreed at multidisciplinary team meeting. This case underscores the essential role of immunohistochemistry in distinguishing gastric schwannoma from GIST, and highlights the absence of a consensus surveillance protocol following resection.

胃神经鞘瘤1例。
胃神经鞘瘤是一种罕见的良性间质肿瘤,在影像学上与胃肠道间质瘤(gist)非常相似,尽管生物学行为根本不同。我们报告一位74岁男性,因直肠癌行直结肠切除术,在胃镜检查中偶然发现一个5厘米的外生胃团块。内镜超声引导下细针穿刺有利于神经鞘瘤,患者接受了简单的腹腔镜胃楔形切除术。组织病理学证实为胃神经鞘瘤,边缘清晰,无淋巴结累及;免疫组化检测S100钙结合蛋白(S100)/SRY-box转录因子10 (SOX10)阳性,GIST-1 (DOG1)/CD117 (c-KIT)/平滑肌肌动蛋白(SMA)/desmin阴性,GIST除外。患者恢复良好,2天后出院,经多学科小组会议同意保守内窥镜检查计划(6个月,然后每年一次,持续5年)。本病例强调了免疫组织化学在区分胃神经鞘瘤和GIST中的重要作用,并强调了在切除后缺乏共识的监测方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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