Searchable abstracts of presentations at key conferences in endocrinology

ea0026p606 | Clinical case reports | ECE2011

Primary hypothyroidism due to sublingual thyroid associated with growth failure, hyperprolactinemia and pituitary enlargement

Loghin A , Florescu A , Moisii L , Stefanescu C , Galesanu C

Introduction: Thyroid tissue may be found anywhere along the course of thyroglossal duct. Sublingual thyroid is a rare type of ectopic thyroid tissue resulting from failure of the embryonic development and migration of the thyroid gland to its normal pre-laryngeal site, reaching between genio-hioid and mylohyiod muscles. In most cases, hypothyroidism develops due to inadequate hormon production. Hypothyroidism may produce pituitary enlargement secondary to thyrotroph hyperplas...

ea0029p399 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

Unusual association between pheochromocytoma, adrenocortical nodular hyperplasia and empty sella: case report

Preda C. , Grigorovici A. , Ciobanu D. , Moisii L. , Vulpoi C. , Ungureanu M. , Leustean L. , Mogos V.

Introduction: Pheochromocytoma occasionally associates with pathological lesions of the adrenal cortex. We report a case of non-functional adrenocortical nodular hyperplasia with a concomitant pheochromocytoma in the controlateral adrenal and empty sella.Case report: We describe the case of a 52 year old women with a history of essential hypertension and type 2 diabetes mellitus. She complained of: nausea, abdominal pain, vomiting and constipation. The c...

ea0026p630 | Clinical case reports | ECE2011

A rare variant of Wolfram syndrome with diabetic microvascular disease, hypergonadotropic hypogonadism and palmar fibromatosis: case report

Preda C , Gaspar I , Ungureanu M-C , Leustean L , Cristea C , Moisii L , Mogos V , Vulpoi C

Introduction: Wolfram syndrome, a very rare condition, is a neurodegenerative disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) which appear in childhood, hampering diagnosis and treatment. Others less frequent features as hypergonadotropic hypogonadism, microvascular disease and local fibromatosis are reported in a male patient diagnosed at the age of 18 years.Case report: An 18-year-old male patient d...