Von Hippel–Lindau Disease Revealed by Bilateral Pheochromocytomas: A Series of 4 Cases and Literature Review
Introduction: Von Hippel–Lindau (VHL) disease is an autosomal dominant genetic disorder predisposing to the development of benign and malignant tumors, notably pheochromocytomas, which are often bilateral and of early onset.
Objective: To describe…...
10.5281/zenodo.18447867