Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep113 | Clinical case reports - Pituitary/Adrenal | ECE2017

Von Hippel Lindau disease in two Turkish families with different mutations

Adaş Mine , Toprak İlkim Deniz , Bayraktarli Recep Yılmaz

Von Hippel-Lindau (VHL) disease is an inherited, autosomal dominant syndrome manifested by a variety of benign and malignant tumors. Herein we describe, two families who had VHL. A 21-year-old man (index case 1) presented with bilateral adrenal mass, serendipitously discovered by radiologic examination. He had newly diagnosed arterial hypertension. His family history was significant for his mother who had operated for pheochromocytoma, his two uncles who had experienced cerebr...