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Gastric Inflammatory Myofibroblastic Tumor: a Case Report

Overview
Journal Surg Case Rep
Specialty General Surgery
Date 2024 Mar 15
PMID 38485843
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Abstract

Background: Inflammatory myofibroblastic tumor (IMT) of the stomach is an uncommon mesenchymal neoplasm. We present a case of gastric submucosal tumor (SMT) where the final diagnosis was IMT.

Case Presentation: A 69-year-old man presented with a 24-mm SMT on the posterior wall of the middle third of the stomach that was detected by screening upper gastrointestinal endoscopy. Abdominal contrast-enhanced computed tomography showed that the tumor was well-enhanced. Although endoscopic ultrasonography-guided biopsy was performed, the histological diagnosis was not confirmed preoperatively. Since the tumor was clinically suspected to be a gastrointestinal stromal tumor, we performed gastric wedge resection by laparoscopic-endoscopic cooperative surgery. Pathologically, proliferative spindle cells with a positive reaction for smooth muscle actin, negativity for c-kit, desmin, s-100, CD34, STAT-6, β-catenin and anaplastic lymphoma kinase 1 were identified. Hence, the tumor was finally diagnosed as an IMT originating from the stomach.

Conclusions: When an SMT of the stomach is identified, the possibility of gastric IMT should be considered.

Citing Articles

A Diagnosis of Gastric Inflammatory Myofibroblast Tumor: A Challenge Like No Other!.

Chukkalore D, Loeffler J, Rabah H, Amarnath S, Al Moussawi H, Deeb L ACG Case Rep J. 2024; 11(7):e01416.

PMID: 38988714 PMC: 11236408. DOI: 10.14309/crj.0000000000001416.

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