Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep1182 | Thyroid | ECE2024

Clinical progression and differential diagnosis of an uncommon delayed-onset thyroid eye disease in a patient with graves’ disease: a case report

Mouhaymen MISSAOUI Abdel , Charfi Nadia , Soomauroo Siddiqa , Maalej Souhir , Khochtali Rihab , Abid Mohamed , Rekik Nabila

Introduction: Thyroid eye disease (TED) is the major extra-thyroidal manifestation of GravesÂ’ disease (GD). The delayed onset of TED after hyperthyroidism resolution and the decline in TRAb levels is a rare occurrence, necessitating the exclusion of other underlying orbital inflammatory diseases.Case Report: A 59-year-old non-smoking female patient presented with thyrotoxicosis symptoms (fatigue, palpitations, resting tremors) persisting for three m...

ea0090ep855 | Pituitary and Neuroendocrinology | ECE2023

Risk of neoplasms in acromegaly : a monocentric retrospective study

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Charfi Nadia , Mejdoub Nabila , Ben Salah Dhoha , 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, cardiometabolic disturbances and an increased neoplastic risk. This study aims to assess the tumorigenic potential of GH excessive secretion.Patients and Methods: We conducted a retrospective study (1997-2020) at the Endocrinology department of Hedi Chaker...

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,...

ea0090ep901 | Pituitary and Neuroendocrinology | ECE2023

Obesity prevalence in patients with acromegaly

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Elleuch Mouna , Mejdoub Nabila , Ben Salah Dhoha , 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 determine the prevalence of obesity in patients with acromegalyPatients and Methods : We conducted a retrospective study (1997-2020) at the Endocrinology department of Hedi Chaker University Hospital, Sfa...

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...

ea0099p495 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Comparative analysis of economic burden between cardiovascular and renal complications in hospitalized tunisian patients with type 2 diabetes: a retrospective study

Maalej Souhir , Mnif Fatma , Soomauroo Siddiqa , Mouhaymen Missaoui Abdel , Charfi Nadia , Hadjkacem Faten , Elleuch Mouna , Abid Mohamed , Rekik Nabila

Background: Diabetes mellitus poses a global chronic health challenge, with Tunisia experiencing a concerning surge in type 2 diabetes (T2D) prevalence. Cardiovascular and renal complications are prominent and severe consequences associated with T2D. Evaluating the costs related to managing these complications is crucial to enhance care quality, optimize resource utilization, and ultimately reduce the growing economic and social burden of this chronic disease.<p class="abs...

ea0099ep563 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Prevalence of metabolic and cardiovascular diseases in Hidradenitis Suppurativa

Cherif Malek , Chaabouni Rim , Bessaad Lina , Mouhaymen Missaoui Abdel , Hammami Fatma , Bahloul Emna , Rekik Nabila , Turki Hamida

Introduction & Objective: Hidradenitis Suppurativa (HS), or VerneuilÂ’s disease, is a chronic suppurative inflammatory condition. This study aims to determinate the association between HS and metabolic diseases.Materials and Methods: We conducted a retrospective study between January 2012 and December 2022 enrolling all cases of HS in our dermatology department.Results: Over 11 years, we collected 77 cases. The average age ...

ea0099ep988 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Unraveling syndromic diabetes in the context of h syndrome - a rare genetic entity with multisystemic manifestations - case report

Maalej Souhir , Mnif Fatma , Soomauroo Siddiqa , Mouhaymen Missaoui Abdel , Mnif Mouna , Ben Salah Dhouha , Abid Mohamed , Rekik Nabila

Introduction: The H syndrome, an autosomal recessive genodermatosis, is characterized by cutaneous and systemic manifestations resulting from mutations in the SLC29A3 gene (10q22.2), leading to histiocytic infiltration of multiple organs. This study presents a new observation of H syndrome.Observation: We report the case of a 33-year-old patient, born of consanguineous parents, with a history of diabetes diagnosed at the age of 28 and treated with oral a...

ea0099ep993 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Cost of managing complicated diabetic patients in tunisia: a retrospective study in a hospital setting

Maalej Souhir , Mnif Fatma , Mouhaymen Missaoui Abdel , Soomauroo Siddiqa , Boujelben Khouloud , Mnif Mouna , Ben Salah Dhouha , Abid Mohamed , Rekik Nabila

Background: Diabetes mellitus presents a pervasive global health challenge, and Tunisia grapples with a concerning upswing in the prevalence of type 2 diabetes (T2D). Cardiovascular and renal complications stand out as prevalent and severe outcomes linked to T2D. Evaluating the costs associated with managing these complications in T2D patients is pivotal for improving care quality, optimizing resource allocation, and ultimately mitigating the escalating economic and social bur...