Endocrine Abstracts

Introduction: Pheochromocytoma represents only 5% of adrenal incidentalomas. It is malignant in only 10% of cases. We report a case of pheochrompcytoma with suspucion of double cortico-meullary component or an ectopic secretion of CRH in the context of neurofibromatosis type1Observation: A26year old woman with a history of unilateral renal lithiasis, colic and breast neoplasia, with no notable personal history, consulted for right lumbar pain. An abdomin...

Introduction and aim: Diabetic foot (DF) is associated with increased morbimortality and cost of diabetes management. The aim of this study is to describe the epidemiological, clinical and paraclinical characteristics and follow-up outcomes of patients with diabetic foot in a Tunisian center.Methods: It is a monocentric retrospective study of 210 patients with diabetic foot followed at the endocrinology department of the Hedi Chaker Sfax University Hospi...

Introduction and aim: Dopamine agonists (DA) are prescribed as first-line treatment for prolactinomas and are generally effective and well tolerated. However, the degree and quickness of therapeutic response is variable among patients. The aim of this work is to study the predictive factors of biological remission in patients with prolactinoma treated with DA. Methods: A single-center, retrospective and analytical study of patients with prolactinoma foll...

Introduction: Polycystic ovary syndrome (PCOS) is a common endocrinopathy affecting women of reproductive age. PCOS has two phenotypes, obese and lean, the latter being a much less common presentation of the syndrome.Aim: Compare PCOS outcomes in patients with obese PCOS and patients with lean PCOS.Methods: A retrospective, single-center, descriptive and comparative study including patients with PCOS followed at the endocrinology d...

Introduction: Inappropriate glucocorticoid replacement therapy results in higher mortality rates in patients with Addison disease (AD), predominantly due to higher prevalence of cardiovascular diseases, disturbed glycometabolic state and altered anthropometric parameters. The aim of this study was to assess the impact of life-long corticosteroid exposure on anthropometric parameters in patients with AD.Patients and Methods: This Tunisian cross-sectional ...

Introduction: Prolactinoma is the most common secretory pituitary adenomas. It has clinical and biological characteristics that depend on age, gender and tumor size. Prolactinoma of the old subject is a rare clinical form that was not sufficiently treated in the literature.Materiels and methods: It is a retrospective study including 77 cases of prolactinoma among which 3 cases aged over than 65 years. The collection of data was made between 2000 and 2017...

IntroductionSolid pseudopapillary tumors (SPT) of the pancreas area rare exocrine pancreatic tumor behaving in a low-grade fashion, with limited local invasion risk and a rare metastatic evolution. They mainly affect young women. Their etiopathogenesis remains uncertain. We report the case of a 15-year-old boy, having congenital anomalies, who presented a solid and pseudopapillarytumour of the pancreas.Case report<p class="abst...

IntroductionPrimary ovarian failure currently represents an increasingly frequent cause for consultation in endocrinology, from 4 to 18 % of the causes of primary amenorrhea and 10 to 28 % of the causes of secondary amenorrhea.ObjectivesIn this context, we report a retrospective study of 50 patients followed between 2000 and 2020 for early menopause, in order to assess the etiologies and risk factors favourin...

IntroductionThe diabetic foot represents a public health problem with very important direct and indirect expenses. Multidisciplinary care and monitoring is essential. The aim of this Study was to describe the management of the diabetic foot in the endocrinology department.Materials and methodsIt was a retrospective study carried out in the Endocrinology and Diabetology department of the Hédi Chaker unive...

INTRODUCTIONType IV hypertriglyceridemia (HTG IV) or endogenous HTG is a rare inheriteddisorder of the lipoprotein metabolism due to increased hepatic triglyceride synthesis(TG). Although HTGIV is not usually expressed until adulthood, it might be unmasked earlier. We report the case of an early and severe HTGIV complicated with chronic pancreatitis.Case reportA 6-year-old childwith no particular history was ...