Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1069 | Thyroid | ECE2023

Thyroid pathology and hypofertility

Ben Salah Raida , Hadjkacem Faten , Somauroo Seddiqa , Abid Mohamed , Bahloul Zouhir

Introduction: Thyroid pathology is common in women of reproductive age. Evaluation of thyroid function is classically recommended in cases of recurrent abortion. The presence of dysthyroidism or antithyroid antibodies increases the risk of abortion. We report two observations of hypofertility related to thyroid pathology and discuss the therapeutic course.Case 1: A 33 year old woman was referred for etiological investigation of recurrent abortion. She pr...

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...

ea0073aep24 | Adrenal and Cardiovascular Endocrinology | ECE2021

One train may hide another: Scleromyositis in a patient with peripheral adrenal insufficiency

Abir Derbel , Mouna Snoussi , Mouna Guermazi , Feten Frikha , Chifa Dammak , Salah Raida Ben , Sameh Marzouk , Zouhir Bahloul

IntroductionPatients with primary adrenal insufficiency (PAI) may have musculoskeletal symptoms. However, the association of such endocrinopathy with scleromyositis is extremely rare and has not been reported formerly to our acknowledge. Herein we report this association.Case reportA 32-years old female with one year history of profound global weakness was referred to internal department in April 2006, for su...

ea0073aep99 | Calcium and Bone | ECE2021

Recurrent primary hyperparathyroidism due to ectopic retropharygeal adenoma

Mouna Guermazi , Mouna Snoussi , Abir Derbel , Feten Frikha , Chifa Dammak , Salah Raida Ben , Sameh Marzouk , Zouhir Bahloul

IntroductionThe ectopic parathyroid adenoma (EPTA) is the most common cause of failed parathyroid surgery. Most often localisations are intra-thymic and intra-mediastinal adenomas. We report a rare presentation of a symptomatic parathyroid adenoma located in ectopic retropharyngeal position diagnosed after surgical treatment of primary hyperparathyroidism (PHPT).ObsevationA 42-year-old female was referred to ...

ea0073aep485 | Pituitary and Neuroendocrinology | ECE2021

Hypopituitarism in systemic diseases

Abir Derbel , Mouna Guermazi , Mouna Snoussi , Chebbi Donia , Chifa Dammak , Feten Frikha , Salah Raida Ben , Sameh Marzouk , Zouhir Bahloul

IntroductionHypopituitarism is a rare condition defined by loss of pituitary function due to involvement of hypothalamus and/or pituitary gland by infiltrative diseases mainly sarcoidosis and Langerhans cell histiocytosis (LCH). Central diabetes insipidus is the most frequent manifestation of LCH (10–50%) and rarely in neuro-sarcoidois. Herein, we describe 2cases of hypopituitarism due to neuro-sarcoidosis and LCH.Case 1<p...