VHL disease is a syndrome that is defined by a variety of tumors such as cerebellar hemangioblastomas, renal cell carcinomas, phaeochromocytomas, pancreatic adenomas and ear, nose, and throat (ENT) adenomas. This disease is genetic and inherited in an autosomal dominant fashion, and can present in childhood, adolescence, or adult life. This study describes the presentation, natural history, and manifestations of patients attending our institutions with this condition.
Forty-three patients were referred to the VHL clinic. These patients ranged from 18 to 68 years old. The most frequent mode of presentation was neurological signs with genetic diagnosis in 15 patients (34%), cerebellar hemangioblastoma (11%), spinal hemangioblastoma (11%), renal cell carcinoma ( 4%), pheochromocytoma ( 2%), retinal changes (3%) and auditory cyst ( 2%)
The University of Florida Health is a referral center for nephrology, urology, and neurosurgery and deals with a significant proportion of patients diagnosed with VHL in Florida. This study highlights the significant burden of this illness and emphasizes the importance of screening for these renal/CNS and ENT complications. This study also highlights the importance of family screening in diagnosing this condition. As well as the importance of designated VHL clinics in taking care of individuals and families affected by VHL.