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...

ea0056p1167 | Thyroid cancer | ECE2018

TSH level and risk of malignancy in patients with thyroid nodules with Bethesda IV Cytopathology System

Moujir Carolina Fernandez-Trujillo , Perez Carlos Antonio Rodriguez , Arencibia Dunia Marrero , Plasencia Yaiza Lopez , Zaballo Julio Perez , Galvan Jose Cabrera , Mogollon Francisco Javier Novoa , Cortes Mauro Boronat

Introduction: Fine needle aspiration biopsy (FNAB) is the mainstay diagnostic procedure for evaluation of thyroid nodules, but it doesn’t permit to distinguish between benign and malignant follicular lesions (category IV in the Bethesda Cytopathology System). Some reports have suggested an association between increased serum levels of TSH and thyroid cancer. However, the specific relationship between TSH and malignancy has been scarcely studied in follicu...