Searchable abstracts of presentations at key conferences in endocrinology

ea0035p546 | Endocrine tumours and neoplasia | ECE2014

Pheochromocytoma and neurofibromatosis type 1: description of case

Monteiro Ana Margarida , Alves Marta , Souto Selma , Manso Fernando , Cruz Mariana , Marques Olinda

Introduction: The pheochromocytomas are rare neuroendocrine tumors that can occur sporadically or, in about 30% of cases, in the context of family syndromes. Ten percent are malignant. Neurofibromatosis type 1 is an autosomal dominant disease that is associated with the occurrence of these tumors. Pheochromocytoma appears at 0.1– 5.7% of patients with neurofibromatosis type 1, and are usually solitary and benign lesions.Clinical case: A 50-year-old ...