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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastrointest Surg. Jul 27, 2026; 18(7): 119186
Published online Jul 27, 2026. doi: 10.4240/wjgs.v18.i7.119186
Pancreatic lymphoepithelial cyst with sebaceous differentiation-encountering and management of these rare tumours: A case report and review of literature
David Badovinac, Boštjan Luzar
David Badovinac, Department of Abdominal Surgery, University Medical Centre Ljubljana, Ljubljana 1000, Slovenia
David Badovinac, Department of Surgery, Faculty of Medicine, University of Ljubljana, Ljubljana 1000, Slovenia
Boštjan Luzar, Institute of Pathology, Faculty of Medicine, University of Ljubljana, Ljubljana 1000, Slovenia
Author contributions: Badovinac D and Luzar B were responsible for literature review, manuscript conceptualization and writing; all authors have read and agreed to the published version of the manuscript.
Informed consent statement: Informed consent of the patient for publication of his case was obtained.
Conflict-of-interest statement: The authors declare no conflict of interest.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Corresponding author: David Badovinac, PhD, Department of Abdominal Surgery, University Medical Centre Ljubljana, 7 Zaloška c, Ljubljana 1000, Slovenia. david.badovinac@kclj.si
Received: January 21, 2026
Revised: February 17, 2026
Accepted: April 13, 2026
Published online: July 27, 2026
Processing time: 187 Days and 22.7 Hours
Abstract
BACKGROUND

Lymphoepithelial cysts (LECs) of the pancreas are rare, benign cystic lesions with unclear pathogenesis, and their diagnostic workup is often challenging. LECs with sebaceous differentiation are even more uncommon. They are typically solitary and asymptomatic, found in men and diagnosed incidentally. While imaging modalities and endoscopic ultrasound (EUS) may help identify cystic lesions of the pancreas, LECs can resemble other entities, making accurate preoperative diagnosis difficult. Final diagnosis is usually confirmed only after resection.

CASE SUMMARY

A 74-year-old male was incidentally diagnosed with an asymptomatic cystic lesion of the pancreas tail. While there were no deviations in laboratory workup or clinical examination, magnetic resonance imaging and EUS identified a cystic lesion 37 mm in diameter and filled with concentric nodules within fluid. Mucin was found within the cyst at biopsy, and mucinous cystic neoplasm was suspected. Laparoscopic distal pancreatectomy with splenectomy was performed, and pathological examination of the specimen identified an LEC with sebaceous glands.

CONCLUSION

This article emphasizes the importance of recognizing the distinct characteristics of pancreatic LECs to help clinicians make more informed decisions and avoid unnecessary interventions. Continued reporting of similar cases is vital to improve our understanding and refine diagnostic strategies for these rare pancreatic lesions.

Keywords: Lymphoepithelial cyst; Cystic lesions of the pancreas; Sebaceous glands; Diagnostic workup; Surgical resection; Overtreatment; Case report

Core Tip: This article provides a review of the available literature on extremely rare lymphoepithelial cysts (LECs) of the pancreas, accompanied by reporting management of a patient with such a lesion with sebaceous glands. Pancreatic LECs with sebaceous differentiation are benign and lack malignant potential, but they mimic mucinous cystic lesions radiologically and cytologically, often leading to unnecessary surgery. Thorough pathological examination of the resected specimen is important, as the mechanism of pancreatic LECs in not fully understood. Thus, every reported case may contribute to a better understanding of this rare disease.

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