Inherited disorder causing multiple tumours, both benign and malignant, in the central nervous system (CNS) and viscera
Aetiology
- Autosomal dominant mutation in VHL gene which leads to accumulation of HIF proteins and stimulation of cellular proliferation
Clinical presentation
- May be diagnosed from family history and genetic testing
- May present with symptoms of the various tumours
- Range of vascular tumours
Investigations
- Regular and lifelong surveillance for tumours
- Genetic counselling/testing of family members
Management
- Manage tumours appropriately