Schwannoma: A Rare Case of Submucosal Gastric Tumor

Author:

Fugărețu Cosmina12ORCID,Mișarca Cătalin12,Petcu Lucian1,Șoană Raluca3,Cîrnațiu Andrada1,Surlin Marin Valeriu45ORCID,Patrascu Stefan45ORCID,Ramboiu Sandu45

Affiliation:

1. 1st General Surgery Department, Brașov County Emergency Clinical Hospital, 500326 Brașov, Romania

2. Faculty of General Medicine Brașov, Transilvania University, 500036 Brașov, Romania

3. Pathological Anatomy Department, Brașov County Emergency Clinical Hospital, 500326 Brașov, Romania

4. 1st General Surgery Department, Emergency Hospital of Craiova, 200642 Craiova, Romania

5. Faculty of General Medicine Craiova, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania

Abstract

Schwannoma is a tumor that originates from the Schwann cells that surround a neuron’s axon. This tumor is very rare in the gastrointestinal tract and develops submucosally from intestinal nerve plexuses. The most common location for gastrointestinal schwannomas is the stomach, where they account for only 0.2% of gastric tumors. We present the case of a 56-year-old asymptomatic patient who was diagnosed, following a routine ultrasound examination, with an abdominal tumor. An abdominal MRI confirmed the gastric origin of the tumor. Although a subsequent upper-digestive endoscopic ultrasound was performed, a definitive diagnosis could not be established. Thus, a laparoscopic wedge resection of the stomach was performed. The immunohistochemical examination of the tumor established the diagnosis of benign schwannoma. Despite the availability of advanced endoscopy and imaging techniques, the diagnosis of gastric schwannoma is very rarely preoperative. The immunohistochemical identification of S-100 on the surgical specimen confirmed the diagnosis.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Gastric schwannoma;Journal of Gastrointestinal Surgery;2024-08

2. Gastric schwannoma: a case report;Journal of Surgical Case Reports;2024-03

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