Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep1137 | Thyroid | ECE2022

Graves’ orbitopathy: clinical evaluation and therapeutic aspects

AFFES Sofien , Saloua Ben Amor , Mona Rekik , Amar Nadia Ben , Kacem Faten Hadj , Amira Trigui

Introduction: Graves’ disease is a common autoimmune disease that can be complicated by orbital damage sometimes threatening the visual prognosis. We report the case of a patient with Graves’ orbitopathy and we discuss the difficulties of clinical evaluation and therapeutic management.Case report: A 68-year-old woman presented to our department complaining of eye protrusion and progressive vision reduction in both eyes. She has had a history of...

ea0090ep541 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Insulin intolerance: Adipose panniculitis

Lachiheb Nabil , Mouna Elleuch , Cyrine Chehaider , Nadia Charfi , Kacem Faten Hadj , Mohamed Abid

Introduction: Besides insulin allergy, several other forms of insulin intolerance are possible. Adipose panniculitis (AP) is an acute form.Purpose: Describe the clinical, paraclinical and evolution of AP.Clinical case: 64-year-old patient, type 2 diabetic for 24 years on premixed human insulin for 10 years. He consults for itchy erythematous lesions at the insulin injection sites. The lesion begins with an immediate pruritus then a...

ea0090ep808 | Pituitary and Neuroendocrinology | ECE2023

Infectious manifestations during neuro-gastrointestinal mitochondrial encephalopathy: about 2 patients

Nabil Lachiheb , Ines Bartegi , Ichrak Bougharriou , Hmida Salma Ben , Kacem Faten Hadj , Mouna Mnif , Mohamed Abid

Introduction: Mitochondrial neuro-gastro-intestinal encephalopathy (MNGIE) is a rare autosomal recessive disease caused by a mutation in the TYMP gene.Patients-methods: Retrospective study including 2 cases (brother and sister) followed for MNGIE confirmed by genetic study at the endocrinology department of Sfax.Results: -> 1st case: 25-year-old man, follow-up for diabetes, dilated cardiomyopathy, renal lithiasis, MNGIE.<p ...

ea0063p805 | Thyroid 2 | ECE2019

Predisposition to autoimmune thyroid diseases within a Tunisian multiplex family

Chabchoub Ghazi , Sefi Wajdi , Charfi Nadia , Kacem Faten Hadj , Mnif Mouna , Keskes Leila , Abid Mohamed

Autoimmune thyroid disease (AITD), including Graves’ disease (GD) and Hashimoto’s thyroiditis (HT), is caused by multiple genetic and environmental factors. The clinical and immunological features of GD and HT are distinct; however, there are multiplex families with both GD and HT. In order to study the genetic susceptibility factors to AITDs, we have followed up 115 control members belonging to a large Tunisian family with a high prevalence of AITDs (Akr family) dur...

ea0063p987 | Diabetes, Obesity and Metabolism 3 | ECE2019

Epidemiological, clinical and biochemical characteristics of metabolic syndrome in adults living in South of Tunisia

Chabchoub Ghazi , Gargouri Imene , Kacem Faten Hadj , Charfi Nadia , Mnif Mouna , Keskes Leila , Abid Mohamed

The metabolic syndrome (MetS) is a constellation of physiological and biochemical abnormalities characterized by obesity, hyperglycaemia, elevated triglycerides and decreases in high density lipoprotein cholesterol (HDL-C), and hypertension. The MetS promotes atherosclerosis, and increases the risk of developing diabetes and cardiovascular disease (CVD), as well as rates of mortality. Thus, it has become one of the major public health challenges worldwide. In Tunisia, few stud...

ea0063p1213 | Thyroid 3 | ECE2019

Hyperthyroidism and hepatic dysfunction: the impact of congestive heart failure

Benothman Wafa , Kacem Faten Hadj , Gargouri Imen , Elleuch Mouna , Mnif Fatma , Abid Mohamed

Introduction: Hyperthyroidism (HT) has been associated with hepatic dysfunction in the presence or absence of congestive heart failure (CHF). Our objective is to study the correlation between the clinical and biological presentation of hepatic abnormalities and the cardiac status.Patients and methods: This retrospective study included 17 patients hospitalized in the endocrinology department of Hedi Chaker Hospital in Sfax over 20 years (1997–2017). ...

ea0037ep1239 | Clinical Cases–Pituitary/Adrenal | ECE2015

A cystic lesion of the adrenal gland mimicking hydatid cyst

Kacem Faten Hadj , Ammar Mouna , Maalej Ayman , Cheikrouhou Nesrine , Charfi Nadia , Abid Mohamed

Introduction: Adrenal cystic lesions are uncommon and mostly identified incidentally during radiological investigations or at surgery for unrelated reasons. Its incidence varies between 0.064 and 0.18%. Adrenal cysts are classified as endothelial cysts, pseudocysts, epithelial cysts, and parasitic cysts.Case report: A 45-year-old female with a past medical history of systemic hypertensive disease for 2 years, presented with recurrent abdominal pain durin...

ea0073aep628 | Thyroid | ECE2021

Graves’ disease in patients with autoimmune polyendocrine syndrome type 3

Kacem Faten Hadj , Ben Salah Raida , Abir Derbel , Sara Chouaib , Zouhir Bahloul , Mohamed Abid

IntroductionType 3 autoimmune polyendocrine syndrome (APS-3) is defined by the presence of an autoimmune thyroid disease and another autoimmune illness, excluding Addison’s disease; this is a frequent combination. Graves’ disease (GD) is an autoimmune disorder affecting approximately 0.5% of general population. It’s occurrence in autoimmune polyendocrine syndrome (APS) is less common than Hashimoto thyroiditis. The aim of our study was to ...

ea0073aep654 | Thyroid | ECE2021

Autoimmune polyendocrine syndrome in patients with thyroid autoimmunity

Kacem Faten Hadj , Abir Derbel , Sara Chouaib , Mohamed Abid , Ben Salah Raida , Zouhir Bahloul

IntroductionAutoimmune Polyendocrine Syndrome (APS) is defined by the presence of 2 or more autoimmune induced endocrine failures in a single patient. There are 4 types of APS: type1 including chronic muco-cutaneous candidiasis, hypoparathyroidism, Addison disease (AD) and ectodermal dystrophy, APS type 2 and 3 containing autoimmune thyroide disease (AITD), type1 diabetes (DT1) with (type2) or without adrenal failure (type3) and type 4 not falling into t...

ea0073ep188 | Thyroid | ECE2021

ANCA vasculitis: a rare and serious complication of Benzylthiouracil

Ben Salah Raida , Kacem Faten Hadj , Imen Chabchoub , Frikha Faten , Abid Mohamed , Bahloul Zouhir

IntroductionVasculitis with antineutrophilic cytoplasmic antibodies (ANCA) has been reported in patients treated with anti-thyroid drugs, especially Propylthiouracil and exceptionally with benzylthiouracil (BTU). We present here a case of ANCA-anti-MPO-associated vasculitis related to BTU.Case presentationA 46 old women was treated with BTU during 18 months for Basedow’s...