Evidence map›Paper›PMID 41536454›Full record

ArticleEuropean journal of case reports in internal medicine2025

A Rare Case of Splenunculus Buried within the Stomach.

Mazen Farhat, Karam Karam, Philippe Attieh, Elie Mina, Zarouhie Meguerian, Elias Fiani, Ihab I El Hajj

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Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mazen FarhatDepartment of Gastroenterology and Hepatology, St George University of Beirut, Beirut, Lebanon.
Karam KaramDepartment of Gastroenterology and Hepatology, University of Balamand, Beirut, Lebanon.
Philippe AttiehDepartment of General Surgery, University of Balamand, Beirut, Lebanon.
Elie MinaDepartment of Pathology, St George University of Beirut, Beirut, Lebanon.
Zarouhie MeguerianDepartment of Gastroenterology and Hepatology, St George University of Beirut, Beirut, Lebanon.
Elias FianiDepartment of Gastroenterology and Hepatology, St George University of Beirut, Beirut, Lebanon.
Ihab I El HajjDepartment of Gastroenterology and Hepatology, St George University of Beirut, Beirut, Lebanon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Accessory spleen, or splenunculus, is a congenital anomaly resulting from failure of splenic anlage fusion during embryonic development. It is most commonly located near the splenic hilum or pancreatic tail and rarely occurs within the stomach wall. Gastric accessory spleen is a rare entity that may mimic submucosal neoplasms such as gastrointestinal stromal tumour, posing a diagnostic challenge. Case presentation: We report the case of a 37-year-old male presenting with a 3-month history of epigastric pain, dyspepsia, and nausea. Endoscopy revealed a 2.5-3 cm submucosal mass in the gastric fundus with intact mucosa, and erosive antral gastritis. Endoscopic ultrasound demonstrated a 22.6 × 17.2 × 23.3 mm hypoechoic, homogeneous lesion arising from the third layer of the gastric wall. Endoscopic ultrasound-guided fine needle biopsy (EUS-FNB) showed lymphoid aggregates with characteristic vascular structures lined by CD8-positive littoral cells and CD68/PGM1-positive macrophages. Immunohistochemistry excluded epithelial, neuroendocrine, and lymphoproliferative neoplasms, confirming the diagnosis of gastric accessory spleen. Discussion: This case is distinctive because the patient had no prior splenectomy or trauma and was diagnosed preoperatively using EUS-guided biopsy-avoiding unnecessary surgery. Gastric accessory spleen remains a rare but important differential diagnosis for submucosal gastric lesions. Recognition of its imaging and histopathologic features can prevent misdiagnosis and overtreatment. Conclusion: Gastric accessory spleen is a benign, rare condition that should be considered in patients presenting with gastric submucosal masses. Non-invasive diagnostic modalities such as EUS-FNB and immunohistochemistry are essential to achieve an accurate diagnosis and to avoid unnecessary surgical resection. LEARNING POINTS: Gastric accessory spleen is a rare, usually incidental finding with no clinical significance.It should be considered as one of the differential diagnoses of gastric subepithelial lesions.Despite the fact that histopathologic evaluation remains the gold standard, both nuclear scintigraphy and enhanced computed tomography scan may be useful in the diagnosis of ectopic splenic tissue.

Indexed as

accessory liverEUSfundusStomachsubmucosal mass

Identifiers

PMID41536454
PMCPMC12799056

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