Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep274 | Clinical case reports - Pituitary/Adrenal | ECE2016

Hereditary Pheocromocytoma-Paraganglioma Syndrome: a case report

Gallego M. Teresa , Vera Lucia , Meoro Amparo , Del Peso Cristina

Introduction: Paraganglioma (PGL) develops from cells of the parasympathetic and sympathetic system. It usually manifests as a slow- growing and painless mass. PGL may be hereditary, benign, malignant, unilateral or bilateral tumors. In most cases PGL is located around the common carotid artery but may also be located within the middle ear or in the abdomen. Non functional retroperitoneal PGL are rare tumors, usually asymptomatic, and can attain big dimensions. Mutations in th...

ea0049ep1415 | Thyroid (non-cancer) | ECE2017

Primary thyroid lymphoma: a differential diagnosis to be considered

Teresa Gallego M , Vera Lucia , Del Peso Cristina , Meoro Amparo , Martin Manuel , Candel Marife , Terol Emilio , Pastor Francisco

Introduction: Primary lymphoma of the thyroid, although rare, should be considered in the differential diagnosis of patients with thyroid nodules or goiter, because its prognosis and treatment differ substantially from that of the other disorders. Thyroid lymphomas are nearly always of the non-Hodking type (70–80% B cell lineage). There is a 4:1 female predominance and the mean and median ages at diagnosis are between 65 and 75 years. Hashimoto’s thyroiditis is the o...