Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep610 | Endocrine-Related Cancer | ECE2022

Insulinoma with confusing imaging : a case report

Belabed Wafa , Mnif Fatma , Missaoui Abdelmouhaymen , Salah Dhoha Ben , Akid Faten Haj Kacem , Mouna Elleuch , Mnif Mouna , Charfi Nadia , Mejdoub Nabila , Abid Mohamed

Introduction: Insulinoma is a rare pancreatic tumor. It is the most frequent cause of organic hypoglycemia due to endogenous hyperinsulinism.Case report: A 55-year-old woman was admitted in our department for the management of a recurrent hypoglycemic coma. Endogenous hyperinsulinic hypoglycemia was confirmed with a spontaneous hypoglycemia. Plasma blood glucose was 0.25 g/l concomitant to a high insulinemia of 31.5 µUI/ml (≥ 3) and C-peptide ...

ea0081ep665 | Pituitary and Neuroendocrinology | ECE2022

Giant prolactinomas: a descriptive study and prognostic analysis

Elleuch Mouna , Frikha Hamdi , Fatma Loukil , Salah Dhoha Ben , Souhir Maalej , Mnif Mouna , Mnif Fatma , Charfi Nadia , Majdoub Nabila Rekik , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Giant prolactinomas (GP), defined as prolactinomas ≥4 cm in maximum dimension, are uncommon, with reported prevalence of 2 to 3% of all prolactinomas. Aim: The aim of this study is to describe clinical and paraclinical characteristics of GP and to identify predictors of therapeutic response.Matherials and methods: A retrospective, single-center, descriptive study including 18 patients with GP followed at the end...

ea0081ep696 | Pituitary and Neuroendocrinology | ECE2022

AQP2 gene mutation C.450T>A in a Tunisian family

Mnif Fatma , Charfi Hana , Abdelhedi Fatma , Bouassida Malek , Akid Faten Haj Kacem , Salah Dhoha Ben , Mnif Mouna , Charfi Nadia , MAJDOUB NABILA REKIK , Elleuch Mouna , Kammoun Hassen , Abid Mohamed

Introduction: The nephrogenic diabetes insipidus (DI) is an entity to be known. It is essential to know its etiologies and especially its therapeutic modalities which are different from those of the central DI. The familial nature of the disease should suggest a genetic origin. In our paper, we are presenting the case of a Tunisian family with genetic nephrogenic DI.Case reports: Our family had a history of neglected polyuro-polydipsic syndrome (PPS), de...

ea0081ep697 | Pituitary and Neuroendocrinology | ECE2022

Endocrine dysfunction secondary to pituitary tuberculoma: a case report

Mnif Fatma , Charfi Hana , Salah Dhoha Ben , Akid Faten Haj Kacem , Charfi Nadia , Majdoub Nabila Rekik , Mnif Mouna , Elleuch Mouna , Abid Mohamed

Introduction: Tuberculosis is an infectious disease that involves any organ. However, the primary pituitary tuberculosis is an extremely rare disease. Intracranial tuberculomas account for 0,15-5% of intracranial space-occupying lesions, of which pituitary as the primary site, and easily misdiagnosed as pituitary adenoma. In this setting, the late diagnosis can result in permanent endocrine dysfunction. We hereby report the case of a patient with pituita...

ea0081ep738 | Pituitary and Neuroendocrinology | ECE2022

Visual impairment in the empty sella syndrome

Fatma Mnif , Zargni Asma , Arbi Kawthar El , Akid Faten Haj Kacem , Salah Dhoha Ben , Charfi Nadia , Mnif Mouna , Majdoub Nabila Rekik , Elleuch Mouna , Abid Mohamed

Introduction: Empty sella syndrome (ESS) is a rare condition in which the sella turcica is partially or completely filled with cerebrospinal fluid. It can be primary or secondary. Ophthalmologic involvement is rare in primary empty sella Syndrome. It is described in only 1.6 to 16% of cases. Patients and methods: We report a retrospective study of 46 cases of ESS collected in the endocrinology department over the period from 1991 to 2020. The clinical an...

ea0081ep748 | Pituitary and Neuroendocrinology | ECE2022

Clinical, paraclinical and genetic features of diabetes insipidus

Mnif Fatma , Charfi Hana , Abdelhedi Fatma , Bouassida Malek , Elleuch Mouna , Salah Dhoha Ben , Mnif Mouna , Majdoub Nabila Rekik , Charfi Nadia , Akid Faten Haj Kacem , Kammoun Hassen , Abid Mohamed

Introduction: Diabetes insipidus (DI) is a rare pathology. The advent of hypothalamic-pituitary MRI has made it possible to make a positive diagnosis by avoiding the water restriction test (WRT). The etiological diagnosis is still a challenge in view of the diversity of diseases involved, which influences the therapeutic management and prognosis.Work Objectives: The objectives of our work were to describe the clinical, paraclinical and genetic features o...

ea0081ep750 | Pituitary and Neuroendocrinology | ECE2022

Neurosarcoidosis and pituitary metastasis of a small cell carcinoma: an unusual association

Mnif Fatma , Charfi Hana , Elleuch Mouna , Salah Dhoha Ben , Charfi Nadia , Mnif Mouna , Majdoub Nabila Rekik , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Pituitary stalk thickening (PST) is often identified on magnetic resonance imaging (MRI), either incidentally or during diagnostic workup of hypopituitarism. Currently, there is no unified standard for the definition of PST. As a reference, a pituitary stalk with width over 3 mm has been used as the diagnostic criterion for PST in recent years. The disease spectrum of PST is quite diverse and can be grouped into three broad categories: neoplastic, inflammatory an...

ea0081ep824 | Pituitary and Neuroendocrinology | ECE2022

What factors predict a favorable response to hormonal therapy in congenital growth hormone deficiency?

Rekik Majdoub Nabila , ARBI Kawthar El , Zargni Asma , Salah Dhoha Ben , Benothman Wafa , Elleuch Mouna , Fatma Mnif , Charfi Nadia , Mnif Mouna , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Growth hormone (GH) treatment in congenital growth hormone deficiency (CGHD) is indicated to improve the prognosis of the statural prognosis. The aim of this study is to identify the predictive factors of a favorable response to GH therapy.Patients & Methods: This is a retrospective study, conducted over a period of 27 years, including 30 patients with CGHD treated with hormonal therapy.Results: The CGHD was diagn...

ea0081ep1104 | Thyroid | ECE2022

Graves’ disease: Particularities in the pediatric population

Ben Salah Dhoha , ARBI Kawthar El , Zargni Asma , Elleuch Mouna , Chehaider Cyrine , Fatma Mnif , Charfi Nadia , Mnif Mouna , Majdoub Nabila Rekik , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Graves’ disease (GD) is the most common cause of hyperthyroidism in pediatric patients, up to 95% in some studies.Observation: We report the observation of a 6-year-old female who consulted for a behavioral disorder made of agitation and lack of concentration. She had a family history of autoimmune thyroid disease. On examination, an accelerated statural growth rate of +2DS was noted. She had a significant palpebral retraction without ...

ea0081ep1131 | Thyroid | ECE2022

Coronary insufficiency during hyperthyroidism: Report of six cases

Elleuch Mouna , Chehaider Cyrine , Teber Sawssen Ben , Salah Dhoha Ben , Soomauroo Siddiqa , Charfi Nadia , Mnif Mouna , Mnif Fatma , Rekik Nabila , Kacem Faten Hadj , Abid Mohamed

Introduction: Cardiothyreosis is the consequence of the effects of excess free thyroid hormones on the vascular wall and myocardium. This complication is the most serious aspect of hyperthyroidism. Rhythm disorders and heart failure are the most frequently noted. The prevalence of coronary insufficiency is lower. The aim of this study is to evaluate the characteristics of coronary insufficiency in patients with hyperthyroidism.Method: This is a retrospec...