成人不典型表现的胃神经鞘瘤1例报告及文献复习。

IF 1.2 Q4 ONCOLOGY
ecancermedicalscience Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI:10.3332/ecancer.2025.1910
Yanet Isabel Carrasco Rojas, Albert Gabriel Turpo Peqqueña, Natalia Camila Zenteno Tejada, Victoria Elena Quispe Pastor, Juan Augusto Martínez San Martín, Evelyn Maria Chambilla Huellcacure
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引用次数: 0

摘要

胃神经鞘瘤(GS)是一种罕见的肿瘤,起源于影响胃肠道的雪旺细胞,由于其非特异性症状,给诊断带来了挑战。我们报告的情况下,61岁的女性提出胃饱和偶尔发作的腹痛。计算机断层扫描显示胃小弯处一实性肿块,最初怀疑为胃肠道间质瘤。手术期间,外生性病变被组织病理学和免疫组织化学鉴定为胃神经鞘瘤。胃上皮下肿瘤的鉴别诊断应考虑GS。其诊断依赖于免疫组织化学,手术切除确保有效治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gastric schwannoma with atypical manifestations in an adult patient: case report and literature review.

Gastric schwannomas (GS) are rare tumours originating from Schwann cells that affect the gastrointestinal tract, posing a diagnostic challenge due to their nonspecific symptoms. We report the case of a 61-year-old female presented with gastric fullness and occasional episodes of abdominal pain. Computed tomography revealed a solid mass in the lesser curvature of the stomach, initially suspected to be a gastrointestinal stromal tumours. During surgery, an exophytic lesion was identified and confirmed histopathologically and immunohistochemically as a gastric schwannoma. GS should be considered in the differential diagnosis of gastric subepithelial tumours. Its diagnosis relies on immunohistochemistry, and surgical resection ensures effective treatment.

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来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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