Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep957 | Thyroid | ECE2022

Did well-controlled hypothyroid patients have necessary good compliance?

Kamoun Elyes , Jemel Manel , Gharbi Radhouen , Hilel Wafa Ben , Kandara Hajer , Kammoun Ines

Introduction: Treatment of primary hypothyroidism relies on a daily intake of levothyroxine, which dosage is determined first by the weight then by TSH levels monitoring. The daily dosage can vary with the cause of the hypothyroidism and the weight. The aim of our study was to determine if the adherence was a factor influencing the dosage of levothyroxine in a group of well-controlled hypothyroid patients.Method: We performed a cross-sectional study incl...

ea0090ep193 | Calcium and Bone | ECE2023

Parathyroid carcinoma: A case report

Maram Ben Salem , Chiboub Marwa , Hilel Wafa Ben , Jemel Manel , Kammoun Ines

Introduction: Parathyroid carcinoma is an uncommon cause of primary hyperparathyroidism. It is responsible of 0.4% to 5% of all cases of primary hyperparathyroidism. Parathyroid carcinoma has a high probability of local recurrence, regional node and distant metastasis and the preoperative diagnosis is challenging.Case presentation: We report a case of a 66-year-old female patient with medical history of hypertension and chronic kidney failure. She was di...

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...