ea0070ep344 | Pituitary and Neuroendocrinology | ECE2020
Halloul Imen
, Othman Wafa Ben
, Kacem Njah Maha
, Saad Ghada
, Benabdelkarim Mzoughi Asma
, Maaroufi Amel
, Chaieb Molka
, Ach Koussay
Introduction: VonHippel Lindau (VHL) disease is an autosomal dominant disorder, responsible of the occurrence of multiple endocrine and non-endocrine lesions. When it comes to this hereditary syndrom., pheochromocytoma and pancreatic neuroendocrine tumors (pNET) require special monitoring and an appropriate treatment, The object of this case report is to highlight the different clinical presentation of the same lesion in the same patient and the difficulties in decisions’...