Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep1067 | Pituitary - Clinical | ECE2017

Nonfunctioning pituitary incidentaloma – delayed onset of acromegaly and concomitant primary adrenocortical insufficiency

Radian Serban , Deciu Diana , Lefter Antonia , Poiana Catalina

Introduction: Pituitary incidentaloma (PitInc), defined as an unsuspected mass observed on imaging studies performed for unrelated conditions. Most such lesions are not clinically significant at initial evaluation and current guidelines recommend periodic follow-up.Aim: To present a rare case of delayed onset of acromegaly in a patient with a nonfunctioning PitInc, raising the question of the utility of prolonged follow-up of PitInc.<p class="abstext...

ea0038p379 | Reproduction | SFEBES2015

Testicular regression syndrome and severe psychiatric disorder – a rare association preventing the optimal management of the endocrine condition

Capatina Cristina , Ghinea Adela , Deciu Diana , Poiana Catalina

Introduction: Testicular regression syndrome (TRS) or vanishing testis syndrome is a rare condition defined as the absence of testicular tissue in a genetic and phenotypic male. Rudimentary accessory structures can be present; in that case, the removal of all remnants is recommended.Case report: Male patient, 39 years old, had initially been evaluated at the age of 8 for persistent bilateral cryptorchidism. The medical documents are lacking except for a ...

ea0059ep14 | Adrenal and steroids | SFEBES2018

Cushing’s syndrome due to primary bilateral macronodular adrenal hyperplasia (PBMAH) - clinical and hormonal characterisation

Vladan Andreea , Radian Serban , Baranga Iuliana , Moraru Catalina , Deciu Diana , Dumitrascu Anda , Hortopan Dan , Iorgulescu Radu , Poiana Catalina

Background: PBMAH is a rare cause of adrenal Cushing’s syndrome, frequently due to aberrant adrenal expression of hormonal receptors.Aim: To describe 6 patients with PBMAH.Methods: Clinical, hormonal and imagistic evaluation.Results: Age at diagnosis of patients (4M/2F) was 50–79 years. One asymptomatic patient was incidentally diagnosed on abdominal CT, two patients had overt Cushing’s (centra...

ea0050ep016 | Adrenal and Steroids | SFEBES2017

‘Connshing syndrome’ as a cause of hypertension: case report

Lefter Antonia , Căpăt´ană Cristina , Deciu Diana , Radian Şerban , Poiană Cătălina

Introduction: An association between primary hyperaldosteronism and autonomous cortisol secretion, tentatively termed ‘Connshing’ syndrome, is becoming increasingly recognized.Aim: To present a case of primary hyperaldosteronism associated with ACTH-independent subclinical Cushing’s.Methods: Clinical examination, biochemical testing and imaging studies.Results: A 49-y...

ea0050ep016 | Adrenal and Steroids | SFEBES2017

‘Connshing syndrome’ as a cause of hypertension: case report

Lefter Antonia , Căpăt´ană Cristina , Deciu Diana , Radian Şerban , Poiană Cătălina

Introduction: An association between primary hyperaldosteronism and autonomous cortisol secretion, tentatively termed ‘Connshing’ syndrome, is becoming increasingly recognized.Aim: To present a case of primary hyperaldosteronism associated with ACTH-independent subclinical Cushing’s.Methods: Clinical examination, biochemical testing and imaging studies.Results: A 49-y...