Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep392 | Reproductive and Developmental Endocrinology | ECE2020

Turner’s syndrome: Clinic, therapeutic and evolutive particularities in a tunisian center

Dorraelguiche Dorra , Ines Kamoun , Kandara Hajer , Mehdi Kalthoum , Wiem Madhi , Jemel Manel

Introduction: Turner’s syndrome (TS) affects 1/2500 female births and it is characterized by growth retardation, dysmorphic syndrome and gonadal dysgenesis. Our objective was to describe the clinical, therapeutic and evolutive features of Tunisian patients with TS.Patients and Methods: It was a retrospective study including 23 patients with TS diagnosed between 1993 and 2019.We noted clinical, therapeutic and evolutive data for each patient.<p ...

ea0070ep400 | Reproductive and Developmental Endocrinology | ECE2020

Efficiency of ceylon cinnamon on insulin resistance parameters in polycystic ovary syndrome

Jenouiz Zeineb , Kandara Hajer , Bendag Nedra , Gharbi Radhouan , Jemel Manel , Kammoun Ines

Introduction: Insulin resistance (IR) is the main pathogenic factor in polycystic ovary syndrome (PCOS) and its complications. Ceylon cinnamon (CC) is an herb with an insulin-sensitizing effect reported in diabetic patients.The aim of our study was to assess the efficiency of CC on the parameters of the IR in patients with (PCOS).Methods: We conducted a prospective interventional study, we included 13 patients with PCOS diagnosed according to the Rotterd...

ea0032p344 | Developmental Endocrinology | ECE2013

Resistant hypertension: about 30 cases

Hasni Yousra , Khochtali Ines , Hadiji Manel Jemel , Marmouch Hela , Sayadi Hanen , Mahjoub Sylvia

Resistant hypertension (RH) is defined as blood pressure above a goal despite adherence to at least three optimally dosed antihypertensive medications of different classes, one of which is a diuretic.Objectives: We investigated the prevalence of true resistant hypertension in our Department of Endocrinology, and we described the clinico-biological features of theses patients.Methods: We performed a retrospective descriptive study. ...

ea0032p345 | Developmental Endocrinology | ECE2013

High blood pressure in young adults: 84 cases

Hadiji Manel Jemel , Hasni Yousra , Braham Dorra , Marmouch Hela , Khochtali Ines , Mahjoub Sylvia

Younger people with high blood pressure are 28% less likely to be diagnosed than older people. Arterial hypertension warrants further investigations to exclude secondary causes of hypertension in young people (aged <40 years).Objectives: We conducted a retrospective descriptive study to investigate the characteristics hospitalized hypertensive young adults (<40 years) in our department.Results: The sample included 84 patien...

ea0056p712 | Clinical case reports - Pituitary/Adrenal | ECE2018

Progressive optic glioma and concomitant precocious puberty: case report

Ben Lagha Jihed , Jemel Manel , Mekni Sabrine , Naceri Taghrid , Kamoun Ines , Ben Salem Leila

Low-grade gliomas are the most common brain tumor in children, accounting for 30–50% of central nervous system tumors in the pediatric age group. They can occur anywhere within the central nervous system (CNS) including the optic pathway (5%). When optic gliomas involve the hypothalamus, patients will often present endocrinopathy. Signs of such involvement can include growth failure and precocious puberty. In this report, we present the case of 8 years three months girls ...

ea0056p713 | Clinical case reports - Pituitary/Adrenal | ECE2018

A singular case of hypohidrotic ectodermal dysplasia associated with acromegaly

Bel Hadj Hassen Hana , Jemel Manel , Mekni Sabrine , Ben Lagha Jihed , Kamoun Ines , Salem Leila Ben

Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder characterized by the faulty development of the ectodermal structure, resulting in most notably anhydrosis/hypohydrosis, hypotrichosis and hypodontia. Affected individuals tend to have sparse scalp and body hair (Hypohidrotic), absent teeth (hypodontia) or small and pointed teeth. HED is associated with distinctive facial features including a proeminent forehead, thick lips, and flattened bridge of the nose. The...

ea0073aep324 | Diabetes, Obesity, Metabolism and Nutrition | ECE2021

Diabetes, a harbinger of pancreatic tumor

Mehrzi Amal , Jemel Manel , Madhbouh Meriem , Chatti Hiba , Madhi Wiem , Kammoun Ines

IntroductionPancreatic cancer is one of the cancers of the digestive tract for which the prognosis has not been improved in terms of early diagnosis. Recent diabetes can be indicative of this pathology.ObservationA 56-year-old man with no notable pathological history who has presented for 04 months a deterioration in general condition with weight loss. On clinical examination: BMI: 17 kg/m2. In bio...

ea0073aep460 | Pituitary and Neuroendocrinology | ECE2021

Pituitary tuberculosis: A clinical challenge

Chatti Hiba Allah , Kammoun Ines , Gharbi Radhouane , Ibrahim Arbaoui , Sonia Nagi , Kandara Hajer , Jemel Manel

IntroductionCerebral tuberculomas are a rare form of tuberculosis due to the hematogenous spread of Mycobacterium Tuberculosis (MT). Pituitary localization is exceptionally uncommon with total reported cases in the literature fewer than a hundred. Symptoms and radiologic features are nonspecific, leading sometimes to misdiagnosis. We report the rare case of a patient diagnosed with a primary pituitary stalk tuberculosis.Observation...

ea0073aep563 | Pituitary and Neuroendocrinology | ECE2021

Invasive Thyrotropin-secreting pituitary adenoma: A case report

Wiem Madhi , Jemel Manel , Said Wadiaa , Mereghni Syrine , Allah Chatti Hiba , Kandara Hajer , Kammoun Ines

IntroductionThyrotropin-secreting pituitary adenoma is a rare cause of hyperthyroidism which must be differentiated from other etiologies of inappropriate TSH secretion.Observation:We report the case of a 49 years old male patient with no particular pathological history, addressed for thyrotoxicosis (weight loss, irritability, thermophobia, dyspnea and palpitation) with no goiter or ophtalmopathy. Echocardiog...

ea0073aep579 | Reproductive and Developmental Endocrinology | ECE2021

Congenital GH deficiency in children: What are the differences between isolated and combined/total and partial somatotropic GH deficiency?

Dorraelguiche Dorra , Jemel Manel , Anis Grassa , Gharbi Radhouane , Kandara Hajer , Kammoun Ines

Introduction Growth hormone (GH ) deficiency is a rare but not exceptional cause of statural delay in children. The results of GH stimulation tests and the exploration of other pituitary axes allow us to conclude on the nature of the deficiency: total or partial and its possible association with other pituitary deficits.MethodsThis is a retrospective descriptive study including 75 patients followed for congen...