Differential diagnosis of submucosal gastric tumors: gastric schwannomas misdiagnosed as GISTs.

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2024-12-18 eCollection Date: 2024-12-01 DOI:10.1093/jscr/rjae793
Mutlu Unver, Suleyman Cağlar Ertekin, Eyüp Kebapcı, Mustafa Olmez, Erhan Ergin, Safak Ozturk, Erkan Sahin, Ragıp Ortac
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Abstract

Schwannomas commonly occur in the head and neck region but are rarely seen in the gastrointestinal tract; the stomach and small intestine are the most commonly involved sites. These tumors are usually misdiagnosed as gastrointestinal stromal tumors (GISTs) before histopathological confirmation due to radiological similarity. GI schwannomas show positivity for S100 protein and vimentin but are negative for CD 117 and CD 34, which helps in differentiating the tumor from GISTs. Case 1: a 70-year-old woman was referred to our hospital by complaints of abdominal pain and discomfort. Upper GI endoscopy demonstrated a protruding lesion at the lesser curvature of the gastric body, and fine-needle aspiration biopsy showed chronic inflammation without malignancy. Since the lesion was suspected to be GIST, this patient had surgery, and a gastric schwannoma was resected successfully. Case 2: a 66-year-old female with anemia and abdominal discomfort was found to have a submucosal elevated mass at the greater curvature of the antrum. Fine needle aspiration biopsy was suggestive of a spindle cell tumor resembling GIST. The patient underwent subtotal gastrectomy with Roux-en-Y reconstruction. Histopathology confirmed schwannoma. It is necessary to differentiate gastric schwannomas from other submucosal tumors of the stomach, especially GISTs. Surgical complete resection of schwannomas usually has a good prognosis with a low probability of recurrence. Though rare, gastric schwannomas should be included in the differential diagnosis of submucosal gastric tumors because the correct identification of this tumor type helps in proper management and evasion of unnecessary extensive surgery.

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胃粘膜下肿瘤的鉴别诊断:胃神经鞘瘤误诊为胃肠道间质瘤。
神经鞘瘤常见于头颈部,但很少见于胃肠道;胃和小肠是最常见的受累部位。由于影像学上的相似性,这些肿瘤在组织病理证实前常被误诊为胃肠道间质瘤。胃肠道神经鞘瘤显示S100蛋白和vimentin阳性,而cd117和cd34阴性,这有助于与胃肠道神经鞘瘤的鉴别。病例1:一名70岁妇女因腹痛不适来我院就诊。上消化道内镜检查显示胃体小弯处有突出病变,细针穿刺活检显示慢性炎症,无恶性肿瘤。由于病变怀疑为GIST,该患者进行了手术,成功切除了胃神经鞘瘤。病例2:66岁女性,贫血,腹部不适,发现胃窦大弯曲处粘膜下肿物升高。细针穿刺活检提示类似GIST的梭形细胞肿瘤。病人接受胃大部切除及Roux-en-Y重建。组织病理学证实为神经鞘瘤。有必要将胃神经鞘瘤与其他胃粘膜下肿瘤,特别是胃肠道间质瘤进行鉴别。神经鞘瘤手术完全切除预后良好,复发率低。胃神经鞘瘤虽然罕见,但应纳入胃粘膜下肿瘤的鉴别诊断,因为正确识别这种肿瘤类型有助于正确处理和避免不必要的广泛手术。
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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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