Diagnosis of Von Hippel-Lindau Syndrome Via Pancreatic Cyst Fluid Next-Generation Sequencing

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Authors: Syedreza Haider, Jonathan Xia
Cited by: 0
References: 12

Abstract

Von Hippel-Lindau (VHL) syndrome is a rare autosomal-dominant tumor predisposition syndrome characterized by benign and malignant neoplasms across multiple organ systems. We report a case where next-generation sequencing (NGS) of pancreatic cyst fluid resulted in the first diagnostic clue to VHL. A 44-year-old woman presented with subarachnoid hemorrhage from cervical hemangioblastoma and incidental finding of multiple pancreas cysts. Endoscopic ultrasound with fine-needle aspiration was performed and standard cyst fluid analysis was nondiagnostic, but cyst fluid NGS identified a pathogenic VHL mutation. This case highlights the utility of cyst fluid NGS in uncovering hereditary cancer syndromes when conventional analyses are inconclusive.

Fields of Study & Subjects

Genetic factors in colorectal cancer Ear and Head Tumors Pancreatic and Hepatic Oncology Research

Publication details

Journal / source
ACG Case Reports Journal
Volume
13
Issue
2
Pages
e01990–e01990
Publication date
1 February 2026
Language
EN