Searchable abstracts of presentations at key conferences in endocrinology

ea0056gp16 | Adrenal Case reports | ECE2018

Pheochromocytoma associated with cutaneous and uterine leiomyomatosis and renal cancer in a patient with a germline mutation in the FH gene

Diaz Marta Moron , Cortes Mauro Boronat , Martin Juan Luis Afonso , Moujir Carolina Fernandez-Trujillo , Lleo Ana Maria Gonzalez , Gonzalez Adriana Ibarra , Martin Nuria Perez , Mogollon Francisco Javier Novoa

Introduction: Most of pheochromocytomas (PCC) and paragangliomas (PGL) are sporadic. However, up to 40% of them have an inherited origin due to germline mutations in at least 15 known PCC/PGL genes, being the VHL and SDHx genes the ones most frequently affected. The fumarate hydratase (FH) is a Kreb’s cycle enzyme encoded by the FH gene.Its inactivating mutations increase intracellular levels of fumarate, leading to tissular pseudohypoxia and transcription of genes involv...