Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep524 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Biermer anemia in a type 2 diabetic not treated with Metformin

Mouna Elleuch , Ghamgui Wissal , Kacem Faten Hadj , Souhir Maalej , Mouna Mnif , Fatma Mnif , Nadia Charfi , Nabila Rekik , Mohamed Abid

Introduction: Anemia is defined by the World Health Organization as a hemoglobin concentration less than 120 g/l in women outside of pregnancy, and less than 130 g/l in men over 15 years of age. It is common in diabetics. It can be due to an autoimmune disease associated with type 1 diabetes, whereas the inflammatory cause is the primary cause in type 2 diabetes.Observation: This is a 75 year old patient, type 2 diabetic for 21 years on insulin analogues...

ea0090ep733 | Pituitary and Neuroendocrinology | ECE2023

Endogenous hyperinsulinemic hypoglycemia: A retrospective analysis of 10 cases

Belabed Wafa , Mnif Fatma , Missaoui Abdel Mouhaymen , Elleuch Mouna , Charfi Nadia , Mejdoub Nabila , Mnif Mouna , Abid Mohamed

Background and aim: Non-diabetic hypoglycemia is a rare entity that regroups several pathologies. Its exact diagnosis is mostly challenging. Endogenous hyperinsulinism is a curable cause that should be thoroughly screened. The objective of our study was to analyze the ethipathological aspects of hypoglycemia by endogenous hyperinsulinism.Patients and methods: We conducted a retrospective study at the Endocrinology department of Hedi Chaker University Hos...

ea0090ep899 | Pituitary and Neuroendocrinology | ECE2023

Ophthalmological complications in acromegaly

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Elleuch Mouna , Mnif Fatma , Mejdoub Nabila , Abid Mohamed

Background and aim: Acromegaly is a rare condition caused by an excessive secretion of growth hormone (GH) and insulin-like growth factor1 (IGF-1), which are responsible for exaggerated somatic growth and cardiometabolic disturbances. This study aims to describe the ophthalmologic complications seen in acromegaly.Patients and Methods : We conducted a retrospective study (1997-2020) at the Endocrinology department of Hedi Chaker University Hospital, Sfax,...

ea0090ep978 | Thyroid | ECE2023

Phenotypic and genetic features of familial thyroid dyshormonogenesis in the Tunisian population

Haj Kacem Akid Faten , Mouhaymen Missaoui Abdel , Soomauroo Siddiqa , Ayadi Younes , Rekik Majdoub Nabila , Mnif Mouna , Abid Mohamed

Objective: To describe the phenotypic and molecular characteristics of familial thyroid dyshormonogenesis (FTDH) in the Tunisian population.Patients and Methods: A retrospective descriptive study including two related (R and K) with high consanguinity whose members are carriers of FTDH. Biological and genetic screening was proposed for all consenting members.Results: FTDH was identified in 11 patients (8 girls, 3 boys) with a mean ...

ea0090ep1049 | Thyroid | ECE2023

Myopathy in hyperthyroidism : a retrospective analysis of 6 cases

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Elleuch Mouna , Mnif Fatma , Mejdoub Nabila , Abid Mohamed

Background and aim: Hyperthyroidism status can be complicated by polymorphic neuromuscular manifestations sometimes revealing. In the majority of cases, these disorders regress during the transition to euthyroidism. We report in this work 6 observations illustrating the neuromuscular manifestations seen in hyperthyroidism.Observations: We report two cases of chronic myopathy: a man and a woman aged 47 and 55 years respectively, hospitalized for hyperthyr...

ea0063p803 | Thyroid 2 | ECE2019

Genome wide linkage scan for autoimmune thyroid disease susceptibility loci in multiplex Tunisian family.

Chabchoub Ghazi , Sefi Wajdi , Maalej Abdellatif , Kacem Faten Hadj , Mnif Mouna , Rebai Ahmed , Abid Mohamed , Keskes Leila

The autoimmune thyroid disease (AITDs) comprises two clinical phenotype, Graves’ disease (GD) and autoimmune hypothyroidism (AIH), which include goitrous [Hashimoto thyroiditis (HT)] and non goitrous forms [Primary idiopathic myxoedema (PIM)]. These disorders are characterized by loss of immunological self tolerance including the presence of a thyroid lymphocytic infiltrate and autoantibodies to thyroglobulin (Tg) and thyroid peroxidase (TPO). Inheritance of AITDs is comp...

ea0063p834 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Familial multiple endocrine neoplasia type 1 revealed by a maxillary swelling

Salah Dhouha Ben , Gargouri Imen , Mnif Fatma , Elleuch Mouna , Charfi Nadia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder caused by mutations in the MEN1 tumor suppressor gene and is characterized clinically by tumors in two or more endocrine glands, such as the pituitary gland, parathyroid glands or pancreatic islets. We describe an atypical presentation of familial hyperparathyroidism evoking the diagnosis of MEN1 in the first place.Observations: We report a three-member family....

ea0063p1097 | Pituitary and Neuroendocrinology 3 | ECE2019

Predictive factor of hypopituitarism in prolactinoma

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

Intoduction: Pitiutary tumor is considered as the first etiology responsable of secondary hypopituitarism. Hypogonadotropic hypogonadism is the most commonly reported lesion.Meterials and methods: It is a retrospective study including 77 cases of prolactinoma. The data collection was done over 17 years, between 2000 and 2017.Results: Gonadotropic deficiency was confirmed in 48 patients (63.6%). A significant negative correlation wa...

ea0063ep103 | Pituitary and Neuroendocrinology | ECE2019

Non-functional pituitary adenoma

Hadjkacem Faten , Ghariani Imen , Gargouri Imen , Mnif Mouna , Rekik Nabila , Njeh Hanen , Mahfoudh Khaireddine Ben , Abid Mohamed

Introduction: The non-functional pituitary adenoma (NFPA) is a benign tumor, which has a progressive development but it is a severe tumor by its neuro-ophthalmological and endocrine repercussions.Patients and methods: It is about a descriptive and retrospective study conducted in 35 patients collected in the endocrinology department of Sfax between January 2000 and December 2017. The diagnosis of NFPA was based on the presence of pituitary adenoma on hyp...

ea0049ep167 | Endocrine tumours and neoplasia | ECE2017

Corticotroph deficiency in patients with insulinoma

Kacem Faten Hadj , Ammar Mouna , Elleuch Mouna , ghorbel Dorra , Abdallah Rihab Ben , Charfi Nadia , Sefi Wajdi , Mnif Mouna , Abid Mohamed

Introduction: The metabolic stressor, hypoglycemia, elicits integrated counterregulatory responses, including activation of the hypothalamic–pituitary–adrenal axis. However, it is suggested that recurring insulin-induced hypoglycemia can impair this counter-regulation. Here we report three cases of patients with isulinoma and corticotroph deficiency.Case reports: The first case, 38-year-old man was referred because of recurrent episode...