Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep1161 | Thyroid | ECE2022

Case report: Amiodarone-induced thyroid dysfunction

Akid Faten Haj Kacem , Trimeche Oumeyma , Missaoui AbdelMouhaymen , Salah Dhoha Ben , Fatma Mnif , Charfi Nadia , Mnif Mouna , Majdoub Nabila Rekik , Elleuch Mouna , Abid Mohamed

Amiodarone is considered by many the most potent antiarrhythmic drug. The other side of the coin is that it’s associated with many side effects including disturbances in the thyroid function, which can be seen in 14 to 18 % of the cases (1). This case is about a 56-year-old male patient with a history of mitral valve disease who was on Amiodarone for 3 years. His personal history was notable with Epilepsy of unknow etiology for which he was on sodium valproate. During fol...

ea0090p64 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Covid-induced relapse of exogenous insulin autoimmune syndrome successfully treated with Rituximab and plasmapheresis

Frikha Hamdi , Mnif Mouna , Ben Salah Dhoha , Dhieb Nesrine , Elleuch Mouna , Mnif Fatma , REKIK Majdoub NABILA , Charfi Nadia , Haj Kacem Akid Faten , Abid Mohamed

Introduction: Exogenous insulin autoimmune syndrome (EIAS) is a rare cause of hypoglycemia in patients with diabetes treated with exogenous insulin. Flares of auto-immune diseases following covid-19 infection have been widely reported.Case report: A 15-year-old type 1 diabetes female patient treated with detemir and glulisine was diagnosed with EIAS based on major glycemic instability and an elevated anti exogenous insulin autoantibody titer of 40 IU (NV...

ea0090p694 | Pituitary and Neuroendocrinology | ECE2023

Management challenges of gestational pituitary adenoma

Fatma Mnif , Trimeche Oumeyma , Mouhaymen Missaoui Abdel , Ben Salah Dhoha , Elleuch Mouna , Haj Kacem Akid Faten , Charfi Nadia , Mnif Mouna , Rekik Majdoub Nabila , Abid Mohamed

Pituitary apoplexy is a rare condition and gestational pituitary apoplexy (GPA) is even more exceptional. Clinical presentation of GPA is often non-specific overlapping with other conditions, making its diagnosis challenging. Additionally, therapeutic management is often limited since it depends on both the mother’s and the fetus’s prognosis. Herein we report of a woman who was diagnosed with GPA and we discuss the management of her case. A 34-year-old woman with no ...

ea0090p711 | Pituitary and Neuroendocrinology | ECE2023

Prevalence and associated factors related to combined hypopituitarism in patients with congenital Growth Hormone deficiency

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Safi Wajdi , Ben Salah Dhoha , Mnif Fatma , Mejdoub Nabila , Mnif Mouna , Abid Mohamed

Background and aim: Congenital Growth hormone deficiency (CGHD) may result from genetic or congenital disorders of pituitary development. It could be isolated or combined with other types of hypopituitarism. This study aims to evaluate the prevalence of combined hypopituitarism and its associated factors in patients with CGHD.Patients and Methods: We conducted a retrospective study (1991-2019) at the Endocrinology department of Hedi Chaker University Hos...

ea0090p196 | Reproductive and Developmental Endocrinology | ECE2023

Metabolic syndrome in Turner syndrome

Haj Kacem Akid Faten , Trimeche Oumeyma , Mnif Mouna , Mouhaymen Missaoui Abdel , Ben Salah Dhoha , Elleuch Mouna , Fatma Mnif , Charfi Nadia , Rekik Majdoub Nabila , Abid Mohamed

Introduction: Turner syndrome (TS) is a feminine chromosomic disease, defined as the partial or total loss of the X chromosome. Classic phenotype includes growth and pubertal retardation as well as a characteristic dysmorphic syndrome. Other accompanying comorbidities are frequently associated with TS such as metabolic diseases: overweight, diabetes, hypertension (HTA) and dyslipidemia. Through this report we aim to determine the frequency of metabolic diseases associated with...

ea0090p203 | Reproductive and Developmental Endocrinology | ECE2023

Predictive factors of infertility among patients with polycystic ovary syndrome

Elleuch Mouna , Frikha Hamdi , Triki Molka , Ben Salah Dhoha , Souleima Trigui , Charfi Nadia , Mnif Mouna , Mnif Fatma , Rekik Majdoub Nabila , Haj Kacem Akid Faten , Abid Mohamed

Introduction: Polycystic ovary syndrome (PCOS) is occurring in approximately one in seven women. Infertility is a major issue in PCOS. Recognizing patients with higher risk of infertility is still a matter of debate.Aim: Study the predictive factors of female infertility in patients with PCOSMethods: A retrospective, single-center, comparative and analytical study including patients with PCOS followed at the endocrinology departmen...

ea0090p445 | Reproductive and Developmental Endocrinology | ECE2023

Auto-immune diseases in Turner syndrome

Haj Kacem Akid Faten , Trimeche Oumeyma , Mnif Mouna , Khochtali Rihab , Ben Salah Dhoha , Elleuch Mouna , Fatma Mnif , Charfi Nadia , Rekik Majdoub Nabila , Abid Mohamed

Introduction: Turner syndrome (TS) is a genetic disease, attributable to the total or partial loss of an X chromosome. The classic phenotype encompasses short stature, hypergonadotropic hypogonadism and dysmorphic features. It’s also associated with other conditions such as autoimmune (AI) diseases. Aim: Herein we aim to determine the frequency of AI diseases in TS and to identify the genetic variants of TS mostly associated with this latter conditi...

ea0090p466 | Reproductive and Developmental Endocrinology | ECE2023

Hyperprolactinemia in Turner syndrome

Haj Kacem Akid Faten , Trimeche Oumeyma , Mnif Mouna , Hamdi Frikha , Ben Salah Dhoha , Elleuch Mouna , Fatma Mnif , Charfi Nadia , Rekik Majdoub Nabila , Abid Mohamed

Introduction: Hyperprolactinemia is a relatively frequent finding. A wide range of conditions can be responsible of this biochemical abnormality. Herein we report a rather rare etiology of hyperprolactinemia which is Turner syndrome (TS).Methods: Aiming to determine the frequency of hyperprolactinemia in patients with TS, we enrolled a retrospective descriptive study in the department of Endocrinology at the Hedi Chaker Hospital. We included patients who...

ea0090ep67 | Adrenal and Cardiovascular Endocrinology | ECE2023

Effect of glucocorticoid replacement dose on bone mineral density in patients with Addison disease: A cross-sectional Tunisian-based study

Boujelben Khouloud , Salah Dhoha Ben , Frikha Hamdi , Elleuch Mouna , Mnif Mouna , Mnif Fatma , Charfi Nadia , Majdoub Nabila Rekik , Kacem Akid Faten Haj , Abid Mohamed

Introduction: Addison disease (AD) is associated with high risk of decreased bone mineral density (BMD) and osteoporosis. Causes are complex, including lifelong glucocorticoid replacement therapy. Several studies have pointed a significant relationship between glucocorticoid dose and low BMD in patients with AD. The aim of our study is to assess the impact of glucocorticoid replacement dose on BMD among Tunisian patients with AD.Patients and Methods: We ...

ea0090ep99 | Adrenal and Cardiovascular Endocrinology | ECE2023

Cardiovascular repercussions of glucocorticoid replacement therapy in patients with Addison disease

Boujelben Khouloud , Salah Dhoha Ben , Frikha Hamdi , Kacem Akid Faten Haj , Mnif Mouna , Mnif Fatma , Charfi Nadia , Majdoub Nabila Rekik , Elleuch Mouna , Abid Mohamed

Introduction: Glucocorticoid replacement therapy may result in long-term morbidities, including cardiovascular diseases which can increase cardiovascular risk. The study was aimed to assess the impact of life-long glucocorticoid replacement therapy on cardiovascular parameters in patients with Addison disease (AD).Patients and Methods: This cross-sectional study was conducted assess cardiovascular events in patients followed for AD for at least 5 years, ...