Searchable abstracts of presentations at key conferences in endocrinology

ea0063p702 | Pituitary and Neuroendocrinology 2 | ECE2019

Cardiovascular and metabolic comorbidities in patients with Cushing’s disease at diagnosis and after long term remission

Amor Bilel Ben , Hasni Yosra , Bayar Ines , Abdelkarim Asma Ben , Kacem Maha , Chaieb Molka , Maaroufi Amel , Ach Koussay

Introduction: Cushing’s disease (CD) is associated with metabolic and cardiovascular comorbidities that can be incompletely resolved after disease remission. Our objective was to evaluate the metabolic and cardiovascular status of patients with MC in remissionPatients and methods: We performed a retrospective study including 15 CD patients cured by pituitary surgery. Patient’s medical records were reviewed and information regarding blood pressu...

ea0063p779 | Thyroid 2 | ECE2019

Medical treatment of Gaves’ disease in Tunisia: comparison of Methimazole and Benzylthiouracil

Hasni Yosra , Chermiti Sondes , El Fekih Hamza , Ben Abdelkarim Asma , Kacem Maha , Chaieb Molka , Maaroufi Amel , Ach Koussay

Background: Antithyroid drugs (ATD) are indicated as first intension in the treatment of Graves’disease (GD). Only two molecules are marketed in Tunisia: Benzylthiouracil (BTU) and Methimazole (MMI). There is still no clear conclusion about the choice of appropriate drug. Our objective was to compare the MMI treatment with the BTU in terms of efficacy and adverse effects (AEs).Methods: It’s a retrospective study. We studied patients with a firs...

ea0063p827 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Congenital adrenal hyperplasia: clinical and hormonal presentation about a Tunisian serie

Hajji Ekram , Hasni Yosra , Othmen Wafa Ben , Abdelkarim Asma Ben , Kacem Maha , Chaieb Molka , Maaroufi Amel , Ach Koussay

Introduction: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders that result from the deficiency of one of several enzymes involved in the steroidogenic pathway for cortisol biosynthesis. The most common cause of CAH, accounting for 90% of cases, is 21-hydroxylase deficiency. The symptoms of disease very depending on the nature and severity of the enzyme deficiency as well as the sex of the individual. Non-classical CAH is generally late onset. Ho...

ea0063p1072 | Pituitary and Neuroendocrinology 3 | ECE2019

Diabetes insipidus as first clinical manifestation of Xanthoma Disseminatum: a case report

Hajji Ekram , Ben Asma , abdelkrim , Marzouk Hajer , Hasni Yosra , Maaroufi Amel , Kacem Maha , Chaieb Molka , Ach Koussay

Introduction: Central diabetes insipidus (CDI) is a heterogeneous condition characterized by the presence of polyuria and polydipsia due to a deficiency of arginine vasopressin. Frequently, CDI is wrongly considered idiopathic if not associated with other signs and symptoms.Case report: We report the case of a 50-year-old woman diagnosed with idiopathic central diabetes insipidus at the age of 34. The MRI scan of the hypothalamus and pituitary gland was ...

ea0063p1086 | Pituitary and Neuroendocrinology 3 | ECE2019

Predictive factors of surgical outcomes in acromegaly

Wafa Badr , Hasni Yosra , Chermiti Sondes , Abdelkarim Asma Ben , Kacem Maha , Chaieb Molka , Maaroufi Amel , Ach Koussay

Introduction: Acromegaly is a chronic disorder usually caused by growth hormone (GH)-secreting pituitary adenomas. Transsphenoidal surgery remains a treatment of choice for restoring GH to normal levels. The aim of this study was to illustrate the relationship between some factors and transsphenoidal surgery outcomes.Patients and methods: We retrospectively analysed the outcome of 31 patients with acromegaly after initial endoscopic transsphenoidal surge...

ea0037gp.16.06 | Diabetes and obesity–Clinical obesity and cardiovascular | ECE2015

Cardiovascular complications in type 1 diabetic patients

Barka Ines , Slim Ines , Cheikhrouhou Nesrine , Ach Koussay , Hasni Yosra , Maaroufi Amel , Kacem Maha , Chaieb Molka , Chaieb Larbi

Background: Although the issue of cardiovascular complications in type 2 diabetic patients is widely discussed and recommendations for such screening are known, it is less common to do so for type 1 diabetes mellitus (T1DM). Unfortunately, the mortality rate due to vascular complications is higher among type 1 diabetic patients than in the general population.Patients and methods: Seventy-six patients with T1DM history over 20 years were included in our s...

ea0037ep418 | Diabetes (complications & therapy) | ECE2015

Achievement of recommended glucose, lipid, and blood pressure targets in patients with type 2 diabetes mellitus

Barka Ines , Slim Ines , Ouerdeni Senda , Ach Koussay , Maaroufi Amel , Hasni Yosra , Kacem Maha , Chaieb Molka , Chaieb Larbi

Background: Patients with type 2 diabetes mellitus (T2DM) have a greater risk for cardiovascular morbidity and mortality than those without T2DM. This risk is even further aggravated if they also suffer from hypertension and/or dyslipidaemia. However, better cardiovascular outcome can be reached by tight control of blood glucose, serum lipids, and blood pressure (BP).Patients and methods: One hundred and nineteen patients were consecutively enrolled. Wel...

ea0070ep50 | Adrenal and Cardiovascular Endocrinology | ECE2020

Adrenal hemangioma: Unusual case of adrenal incidentaloma

Benothman Wafa , Halloul Imen , Saad Ghada , Benabdelkrim Asma , Hasni Yosra , Chaieb Molka , Kacem Maha , Maaroufi Amel , Ach Koussay

Introduction: Adrenal hemangioma (AH) is a benign vascular tumor of the adrenal gland. The adrenal site of an hemangioma is extremely rare occurring only in 0.01% of cases and accounts for 63 reported cases in the literature. AH are often discovered as incidentalomas either by imaging studies or histologic examination. The role of computed tomography (CT) scan and Magnetic resonance imaging (MRI) is important for the differential diagnosis.Case report: W...

ea0070ep344 | Pituitary and Neuroendocrinology | ECE2020

Pancreatic neuroendocine tumors and pheochromocytoma in vonhippel lindau disease

Halloul Imen , Othman Wafa Ben , Kacem Njah Maha , Saad Ghada , Benabdelkarim Mzoughi Asma , Maaroufi Amel , Chaieb Molka , Ach Koussay

Introduction: VonHippel Lindau (VHL) disease is an autosomal dominant disorder, responsible of the occurrence of multiple endocrine and non-endocrine lesions. When it comes to this hereditary syndrom., pheochromocytoma and pancreatic neuroendocrine tumors (pNET) require special monitoring and an appropriate treatment, The object of this case report is to highlight the different clinical presentation of the same lesion in the same patient and the difficulties in decisions&#8217...

ea0070ep366 | Pituitary and Neuroendocrinology | ECE2020

Recurrent cushing’s disease and pregnancy: A case report

Benothman Wafa , Saad Ghada , Halloul Imen , Ben Abdelkrim Asma , Hasni Yosra , Chaeib Molka , Kacem Maha , Maaroufi Amel , Ach Koussay

Introduction: Cushing’s disease (CD) is reported in 60-70% of all patients with Cushing’s syndrome (CS), but occurs only in approximately 33% of the reported CS cases in pregnancy. Nevertheless, despite its rarity, pregnancy in patients with CS can be troublesome because of the risk of maternal-fetal complications.Observation: A 28-year-old female patient was referred to our endocrinology department for a suspected CS with morphological alter...