Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep1166 | Clinical Cases–Pituitary/Adrenal | ECE2015

A rare case of primary empty sella syndrome and growth hormone excess in a patient with neurofibromatosis type 1

Iuliana Pascu Elena , Mihaela Epure , Ioana Arhire Amalia , Sorina Martin , Simona Fica

Introduction: Neurofibromatosis type 1 (NF1) is the most common type of NF, and accounts for about 90% of all cases. Primary empty sella syndrome (ESS) results from herniation of arachnoid mater into the pituitary fossa. Since it has been demonstrated that the small anterior pituitary size reflects loss of neurofibromin expression in the hypothalamus, leading to reduced GHRH, pituitary GH and IGF1 production, we agree that IGF1 and GH increased in our patient can be challengin...

ea0037ep1215 | Clinical Cases–Pituitary/Adrenal | ECE2015

‘Idiopathic'- the truly unknown or yet another hiding place for autoimmunity? A case of central diabetes insipidus in a young woman with Hashimoto thyroiditis

Nila Alexandra , Serbanescu Cristina , Epure Mihaela , Betivoiu Minodora , Martin Sorina , Fica Simona

Introduction: Central diabetes insipidus is a rare, chronic disease characterized by polyuria and polydipsia due to a partial or total vasopressin deficiency (hypothalamic – neurohypophysial system damage). The aetiology can be familial (autosomal dominant inheritance, X-linked recessive traits; mutation of the vasopressin – neurophysin II genes), secondary (tumours, infections, infiltrative diseases, trauma, vascular lesions) and idiopathic (10–30%).<p clas...