Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep270 | Clinical case reports - Pituitary/Adrenal | ECE2016

Differential diagnosis of adrenal insufficiency in a patient with APS syndrome and Rosai–Dorfman disease

Bilic-Curcic Ines , Tripolski Marija , Bacun Tatjana

Primary adrenal insufficiency could be a rare manifestation of antiphospholipid syndrome (APS) and may be a consequence of bilateral adrenal hemorrhage. Rosai–Dorfman disease (RDD) is sinus histiocytosis with massive lymphadenopathy, a rare histiocytic proliferative disorder with a distinctive microscopic appearance. The retro-peritoneum is an infrequent site of involvement as well as extranodal sites.We report a case of a 39-year-old female patient...

ea0041ep318 | Clinical case reports - Pituitary/Adrenal | ECE2016

Usefulness of the 4-mg intravenous dexamethasone suppression test in differentiating Cushing disease from pseudo-Cushing syndrome – a case report

Bilic-Curcic Ines , Tripolski Marija , Bacun Tatjana

Distinguishing Cushing disease from pseudo-Cushing syndrome still remains a challenge, especially in some specific cases when absorption or compliance of dexamethasone used in diagnostical tests are questionable. Several versions of an intravenous (IV) test have been utilized and serve both in the initial and differential diagnosis of Cushing’s syndrome.We report a 59-year-old patient with macroadenoma of pituitary gland (revealed accidentally on MR...

ea0049ep23 | Adrenal cortex (to include Cushing's) | ECE2017

Bilateral adrenal incidentaloma: a diagnostical and therapeutical challenge

Bilic-Curcic Ines , Bacun Tatjana , Tripolski Marija , Zulj Biljana

Incidentally discovered adrenal masses (incidentalomas) present challenges both in diagnosis and management. The bilateral adrenal mass carries a risk of hormone hypersecretion, but it could also present a metastasis from another primary carcinoma or be a part of genetic syndrome.We report a 68 year old patient with bilateral adrenal incidentalomas (revealed accidentally on US, confirmed by abdominal CT in 2015.) left 29 mm, right 33 mm in diameter, radi...

ea0037ep1197 | Clinical Cases–Pituitary/Adrenal | ECE2015

From erectile dysfunction to brain subependymoma: a case report

Bacun Tatjana , Kibel Aleksandar , Degmecic Dunja , Zibar Karin , Pavic Roman

Introduction: Endocrinopathies are rare causes of erectile dysfunction and previously cases of hyperprolactinaemia and pituitary adenomas have been reported.Case report: We present the clinical case of a 27-year old male, married for 4 years with no children, presented with possible infertility and erectile dysfunction which was previously interpreted as caused by a poor social and psychological situation in the family. After additional endocrinological ...