Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep972 | Thyroid | ECE2022

Unilateral graves’ disease : a case report

Khiari Hager , Mekni Sabrine , Adel Meriem , Rojbi Imen , Lakhoua Youssef , Mchirgui Nadia , Nacef Ibtissem Ben , Khiari Karima

Introduction: Graves disease is a frequent etiology of hyperthyroidism. It is defined as a diffuse hyperfunctioning of the thyroid gland caused by an autoimmune disorder. We herein present a rare case of unilateral Graves disease involving the right lobe of the thyroid.Observation: A 44-year-old woman was referred for investigation of subclinical hyperthyroidism revealed by a routine check-up. On physical examination, she had tremor, eyelid retraction, t...

ea0081ep1096 | Thyroid | ECE2022

Cholestatic Hepatitis in Graves’ Disease: A case report

Adel Meriem , Mekni Sabrine , Jridi Maysam , Rojbi Imen , Lakhoua Youssef , Mchirgui Nadia , Nacef Ibtissem Ben , Khiari Karima

Introduction: Thyrotoxicosis is an uncommon cause of cholestasis. It’s a diagnostic challenge considering the broad differential diagnosis. Herein we report a case of Grave’s disease revealed by severe cholestatic jaundice.Observation: A 46 old male with a history of Sickle cell disease complained of diarrhea and significant weight loss for eight months, followed the last month by palpitations, heat intolerance, anxiety, insomnia and progressiv...

ea0090ep72 | Adrenal and Cardiovascular Endocrinology | ECE2023

Characteristics of Hypertension in patients with pheochromocytomas

Abidi Sahar , Mekni Sabrine , Essayeh Sawsen , Hilel Wafa Ben , Faten Cherchir , Mehuirgui Nadia , Nacef Ibtissem Ben , Rojbi Imen , Khiari Karima

Introduction: Pheochromocytomas are rare catecholamine-secreting tumors presenting with various clinical manifestations. Hypertension is the most common finding in pheochromocytomas. It can be either persistent or paroxysmal. Study Design: We conducted a retrospective study of 34 patients who were admitted into the endocrinology department of Charles Nicolle hospital, with a diagnosis of a pheochromocytoma from January 2005 to November 2022.Results: Twen...

ea0090ep89 | Adrenal and Cardiovascular Endocrinology | ECE2023

Pheochromocytomas: presentation and diagnosis

Abidi Sahar , Mekni Sabrine , Essayeh Sawsen , Faten Cherchir , Hilel Wafa Ben , Mchuirgui Nadia , Nacef Ibtissem Ben , Rojbi Imen , Khiari Karima

Introduction: Pheochromocytomas are rare, mostly benign catecholamine-producing neuroendocrine tumors. Clinical manifestations are heterogenous, including persistent or paroxysmal hypertension, sweating, palpitation and headaches known as Menard triad. Diagnostic approach is based on demonstration of catecholamine excess and tumor localization. Our study aimed to describe clinico-biological and radiological features of pheochromocytomas.Methods: We condu...

ea0090ep715 | Pituitary and Neuroendocrinology | ECE2023

Predictive factors of biochemical remission after transsphenoidal surgery in acromegaly

Faten Cherchir , Mekni Sabrine , Essayeh Sawsen , Abidi Sahar , Mchirgui Nadia , Nacef Ibtissem Ben , Rojbi Imen , Khiari Karima

Introduction: Excessive production of growth hormone (GH) in acromegaly is most commonly caused by a somatotroph pituitary adenoma. The therapeutic arsenal is based on selective transsphenoidal adenomectomy (STA) as a first-line treatment. The aim of our study was to determine predictive factors of postoperative biochemical remission in acromegalic patients.Methods: We conducted a retrospective study including 18 acromegalic patients followed-up in the e...

ea0090ep772 | Pituitary and Neuroendocrinology | ECE2023

Characteristics of pituitary insufficiency in acromegaly: report on 28 cases

Abidi Sahar , Mekni Sabrine , Esseyah Sawssen , Cherchir Faten , Mchuirgui Nadia , Rojbi Imene , Nacef Ibtissem Ben , Khiari Karima

Introduction: Acromegaly is a rare condition secondary to the hypersecretion of GH, often by a pituitary adenoma, which can lead to hypopituitarism of varying degrees. Our study aimed to analyze the characteristics of pituitary insufficiency during acromegaly and to search for its predictive factors.Methods: Retrospective study carried out in the endocrinology department of Charles Nicolles Hospital. We recorded 28 patients with acromegaly over a period ...

ea0090ep843 | Pituitary and Neuroendocrinology | ECE2023

Acromegaly: predictive factors for long-term remission

Faten Cherchir , Mekni Sabrine , Essayeh Sawsen , Abidi Sahar , Mchirgui Nadia , Rojbi Imen , Ben Nacef Ibtissem , Khiari Karima

Introduction: The management of acromegaly is commonly based on selective transsphenoidal adenomectomy (STA) as a first-line treatment, and other therapeutic options including somatostatin analogues (SA), dopamine agonists (DA) and radiotherapy as second-line treatment or in case of operative contraindications. The aim of our study was to assess the remission rate and to determine the predictive factors for long-term remission in acromegalic patients.Met...

ea0090ep849 | Pituitary and Neuroendocrinology | ECE2023

Ophthalmological complications in acromegaly: prevalence and associated factors

Faten Cherchir , Mekni Sabrine , Essayeh Sawsen , Ben Hilel Wafa , Mchirgui Nadia , Rojbi Imen , Ben Nacef Ibtissem , Khiari Karima

Introduction: Somatotropin macroadenomas are associated with a considerable risk of ophthalmological impairment. The aim of our study was to determine the prevalence of ophthalmological complications and their associated factors in patients with acromegaly.Methods: We conducted a retrospective study including 28 patients with somatotropin adenomas and followed in the endocrinology department of Charles Nicolle Hospital. Clinical, biochemical and imaging ...

ea0090ep898 | Pituitary and Neuroendocrinology | ECE2023

Acromegaly: Clinico-biological and radiological features

Faten Cherchir , Mekni Sabrine , Essayeh Sawsen , Abidi Sahar , Mchirgui Nadia , Rojbi Imen , Ben Nacef Ibtissem , Khiari Karima

Introduction: Acromegaly results from an autonomous hypersecretion of growth hormone (GH) typically by a pituitary adenoma, commonly revealed by a dysmorphic syndrome. The aim of our study was to describe clinico-biological and radiological features of acromegaly.Methods: We conducted a retrospective study including 28 patients with acromegaly followed in the endocrinology department of Charles Nicolle Hospital. Clinical, biochemical, ophthalmological an...

ea0063p49 | Adrenal and Neuroendocrine Tumours 1 | ECE2019

Endocrine hypertension: before and after treatment of the endocrinopathy

Khiari Marwa , Nacef Ibtissem Ben , Rojbi Imene , Khiari Karima , Jerbi M , Mchirgui Nadia , Lakhoua Youssef , Abdallah Nejib Ben

High blood pressure of endocrine origin remains a rare cause of hypertension. The interest of the research of endocrine hypertension lies in the severity of certain forms and its potentially curable and reversible nature, hence the interest of oriented screening. The aim of our work was to study the profile of endocrine hypertension among a population suffering from secondary diabetes. This is a retrospective descriptive study of 55 patients followed in endocrinology departmen...