Searchable abstracts of presentations at key conferences in endocrinology
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19th European Congress of Endocrinology

Lisbon, Portugal
20 May 2017 - 23 May 2017

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20-23 May 2017, Lisbon, Portugal Further information

Eposter Presentations: Reproductive Endocrinology

Clinical case reports - Pituitary/Adrenal

ea0049ep1085 | Clinical case reports - Pituitary/Adrenal | ECE2017

CHARGE Syndrome: a rare case of hypogonadotropic hypogonadism

Osorio Ana Sofia , Faria Carolina , Barbosa David , Nobre Ema , Bugalho Maria Joao

Introduction: CHARGE Syndrome (CS) is a rare cause of hypogonadotropic hypogonadism (HH), usually diagnosed in paediatric age when pubertal development is compromised. Herein, we report a case that presented a major criterion and three minor criteria.Case report: At age ten, the patient was referred to the paediatric endocrinology unit due to phenotypic alterations and psychomotor and cognitive impairment. She had no family history of consanguinity, inhe...

ea0049ep1086 | Clinical case reports - Pituitary/Adrenal | ECE2017

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

Sagova Ivana , Pavai Dušan , Stančik Matej , Urbankova Helena , Gregova Juliana , Vaňuga Anton , Vaňuga Peter

Combination of Turner syndrome (TS) and classical congenital adrenal hyperplasia (CAH) is rare worldwide. Incidence of CAH - autosomal recessive disorders characterized by enzyme defect of steroidogenic pathway, of which 90% ocuurs in the CYP21A2 gene coding 21-hydroxylase is 1:10000-16000. Incidencie of Turner syndrome is 1:2500 worldwide. Phenotypically, females with TS may present with a wide spectrum of clinical features. They may exhibit short stature, virilization, prema...

ea0049ep1087 | Clinical case reports - Pituitary/Adrenal | ECE2017

A rare case of short-term postpartum primary adrenal insufficiency

Briner Myriam , Gattlen Christina , Kaindl Gunther , Kaufmann Martin Lukas , Zerkiebel Nic , Rudovich Natalia

Aims: Polyglandulare Autoimmune Sydnrome (PAS) is a rare disease and the development during pregnancy is seen even less often. PAS Type II presents with autoimmune adrenalitis and thyroiditis. Symptoms of adrenalitis such as hypotension and hyperpigmentation are overlapping with physiological manifestations during pregnancy making the diagnosis difficult.Clinical presentation: We are reporting the case of a 28-year old prima para prima gravida presenting...

ea0049ep1088 | Clinical case reports - Pituitary/Adrenal | ECE2017

Hypogonadotropic hypogonadism, functional and transitory

Roque Catarina , Serra Filipa , Santos Francisco Sousa , Ferrinho Catia , Capitao Ricardo , Bello Carlos , Vasconcelos Carlos

Functional hypogonadism has been described in association with acute severe medical or surgical illness, subacute recovery and chronic disease. We present a case of transitory hypogonadism manifested during a peri-surgical period. A 42-year-old patient was sent to the endocrinology clinic due to hypertension and a solitary adrenal mass. He was treated with bisoprolol and telmisartan, that he maintains until today. The evaluation favoured non-functional adenoma but during the f...

ea0049ep1089 | Clinical case reports - Pituitary/Adrenal | ECE2017

Congenital adrenal hyperplasia: case series, describing results of initial dexamethasone therapy

Tesic Dragan , Stokic Edita , Medic-Stojanoska Milica , Mitrovic Milena , Tomic-Naglic Dragana , Icin Tijana , Bajkin Ivana , Popovic Djordje , Dusan Vuleta , Vlaski Jovan

Introduction: Congentital adrenal hyperplasia (CAH) comes to adult endocrinologist wheather as transition from pediatritian (Case 3) or as still without diagnosis (Case 1, 2, 4). The aim of this work is to describe typical forms of CAH initially sucessfuly treated with dexamethasone therapy.Case descriptions: Case 1: female, 1972y., presented in 1995y. (23y.) as severe hirsutism and infertility managed by team of gynecologists. She refus...