Searchable abstracts of presentations at key conferences in endocrinology

ea0063p844 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Association of neurofibromatosis type 1 and neuroendocrine tumor

Kacem Faten Hadj , Zargni Asma , Mnif Fatma , Rekik Fatma , Elleuch Mouna , Salah Dhouha Ben , Charfi Nedia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Pheochromocytoma occurs in 0.1–5.7% of patients with Neurofibromatosis type 1(NF1). We report two cases of adrenal pheochromocytoma in patients with NF1.Observation: A 46 year-old male was admitted to our department for further examinations of an adrenal mass. The CT-scan showed two well-defined right adrenal masses measuring each 128×87×86 mm and 60×52×37 mm with central necrosis and calcifications in the biggest o...

ea0063p848 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Synchronous tumours: Neuroendocrine Tumours and Breast cancer

Mnif Fatma , El Arbi Kawthar , Hadj Kacem Faten , Zargni Asma , Elleuch Mouna , Ben Salah Douha , Charfi Nedia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction:: The association of breast cancer and neuroendocrine tumours, in particular pheochromocytoma, is rarely described in the literature. We report a case in a particular context.Observation: This is a 53-year-old patient treated with 6 courses of chemotherapy for T2N3cM0 infiltrating breast carcinoma. She was admitted to our endocrinology department for exploration of a left adrenal incidentaloma, objectified in the extension assessment, measur...

ea0063p1053 | Pituitary and Neuroendocrinology 3 | ECE2019

Prolactinoma and elderly subject: which caracteristics?

Elleuch Mouna , Loukil Fatma , Mnif Fatma , Safi Wajdi , Zargni Asma , Salah Dhouha Ben , Hadjkacem Faten , Mnif Mouna , Rekik Nabila , Charfi Nedia , Abid Mohamed

Introduction: Prolactinoma is the most common secretory pituitary adenomas. It has clinical and biological characteristics that depend on age, gender and tumor size. Prolactinoma of the old subject is a rare clinical form that was not sufficiently treated in the literature.Materiels and methods: It is a retrospective study including 77 cases of prolactinoma among which 3 cases aged over than 65 years. The collection of data was made between 2000 and 2017...

ea0063p1056 | Pituitary and Neuroendocrinology 3 | ECE2019

Pituitary stalk abnormalities: etiology aspects about 28 cases

Mnif Fatma , Safi Wajdi , Kacem Faten Hadj , Elarbi Kawthar , Khanfir Raoudha , Salah Dhouha Ben , Elleuch Mouna , Charfi Nadia , Rekik Nabila , Feki Mouna Mnif , Abid Mohamed

Introduction: The pituitary stalk is the target of various congenital or acquired pathologies. In this context we report a cohort of 28 patients with pathology of the pituitary stalk to analyze their clinical, hormonal and radiological characteristics.Results: The average age of our patients was 28 years with extremes ranging from (15 to 64); Male dominance was noted in 60% of cases. The reason for consultation was either a staturo delay or a pubertal de...

ea0063p1100 | Pituitary and Neuroendocrinology 3 | ECE2019

Outcome of prolactinoma during pregnancy

Elleuch Mouna , Loukil Fatma , Salah Dhouha Ben , Sahnoun Randa , Charfi Nedia , Mnif Fatma , Hadjkacem Faten , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Infertility is a classic consequence of prolactinoma in women. The treatment of hyperprolactinemia allows the restoration of ovulatory cycles and therefore of fertility in 80–90% of cases.Methods and materials: The study is a retrospective cohort study done over 17 years from 2000 to 2017. It includes 77 cases of prolactinomas among which 12 women had one or more pregnancies after the diagnosis of prolactinoma.Re...

ea0063p1175 | Thyroid 3 | ECE2019

Familial autoimmune polyglandular syndrome: a case report

Ben Salah Dhouha , Saafi Wiem , Kacem Feten Hadj , Mnif Fatma , El Arbi Kawthar , Elleuch Mouna , Charfi Nadia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Autoimmune polyglandular syndrome (APS) is an autoimmune disorder that affects many endocrine glands. Until now four categories of APS are identified: APS-I includes at least two out of: mucocutaneous candidiasis, hypoparathyroidism and adrenocortical failure. APS-II, the most frequent, comprises of Addison’s disease, autoimmune thyroid disease and/or type 1 diabetes. APS-III is defined by the presence of autoimmune thyroid disease and other autoimmune disor...

ea0056ep103 | Pituitary and Neuroendocrinology | ECE2018

Unusual association: turner syndrome and anterior pituitary insufficiency in 6 cases

Safi Wajdi , Kacem Faten Hadj , Moalla Mariem , Ghorbel Dorra , Mnif Fatma , Feki Mouna Mnif , Rekik Nabila , Belghith Neila , Abdelhedi Fatma , Kacem Hassen Hadj , Abid Mohamed

Introduction: Turner syndrome (ST) affects 1/2500–1/4000 of female births, its association with congenital malformations is traditional, however the coexistence of hypopituitarism is exceptional. In this context, we report 6 patients; including 3 belonging to the same family and in whom the association of anterior pituitary insufficiency (IAH) to a ST was confirmed.Results: The average age of our patients was 17.2 years (11–31). The ST was sele...

ea0073aep25 | Adrenal and Cardiovascular Endocrinology | ECE2021

Oral and dental manifestation of Allgrove syndrome: A case report

Dhoha Ben Salah , Charfi Hana , Mouna Elleuch , Wajdi Safi , Fatma Mnif , Mouna Mnif , Nadia Charfi , Nabila Rekik , Faten Hadj Kacem , Mohamed Abid

IntroductionTriple-A syndrome, also known as Allgrove syndrome, is a rare autosomal recessive disorder. It is a multisystemic disease with an estimated prevalence of 1 per 1 000 000 individuals The 3 features of this syndrome are achalasia, adrenal insufficiency, and alacrima. Recently, dental impairment has been the subject of several case reports and reviews. However, this abnormality remains under-diagnosed.Purpose<p class="...

ea0073aep70 | Adrenal and Cardiovascular Endocrinology | ECE2021

Metabolic profile and cardiovascular risk assessment in subclinical cushing’s syndrome

Salah Dhoha Ben , Missaoui Abdelmouhaymen , Elleuch Mouna , Trimeche Oumeyma , Mnif Fatma , Charfi Nadia , Mnif Mouna , Mejdoub Nabila , Faten Hadj Kacem , Mohamed Abid

IntroductionSubclinical Cushing’s syndrome (SCS) is an endocrine disorder characterized by an autonomous cortisol secretion in patients bearing adrenal adenomas in the absence of specific signs of hypercortisolism. The cortisol excess is known to be associated with metabolic comorbidities such as obesity, hypertension, glucose intolerance, and dyslipidemia increasing the incidence of cardiovascular events. The objective of this study was to describe...

ea0073aep72 | Adrenal and Cardiovascular Endocrinology | ECE2021

Metabolic impact of glucocorticoid substitution in Addison’s disease

Safi Wajdi , Salah Dhoha Ben , Elmoctar Sidina Mohamed , Mohamed Abdallahi Mohamed Ahmed , Charfi Nadia , Mnif Fatma , Rekik Nabila , Mnif Mouna , Kacem Faten Hadj , Abid Mohamed

IntroductionRecent studies in patients with Addison’s disease have shown that this condition, even if treated, is fraught with significant morbidity and even excess mortality. The objective of our study was to determine the deleterious effects of long-term glucocorticoid replacement mainly on the metabolic level.MethodsRetrospective study, carried out at the Endocrinology and Diabetology Department of H&...