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Scholars Journal of Medical Case Reports | Volume-13 | Issue-11
Radiologic Hallmarks of Von Hippel–Lindau Syndrome: A Case of Multiorgan Involvement
M. Darfaoui, A. El Hadri, Y. Bouktib A. El Hajjami, B. Boutakioute, M. Ouali Idrissi, N. Cherif Idrissi El Ganouni
Published: Nov. 4, 2025 | 29 13
DOI: https://doi.org/10.36347/sjmcr.2025.v13i11.004
Pages: 2675-2676
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Abstract
Von Hippel–Lindau (VHL) syndrome is a rare autosomal dominant disorder resulting from germline mutations in the VHL tumor suppressor gene on chromosome 3p25.3. It predisposes affected individuals to the development of benign and malignant tumors and cysts in multiple organs, including the central nervous system, kidneys, adrenal glands, pancreas, and inner ear. Early radiologic recognition is essential for timely diagnosis, surveillance, and management.