Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep28 | Adrenal cortex | ECE2015

Cushing's syndrome and dyslipidaemia

Azzoug Said , Rabehi Leyla , Hannachi Sara , Medjdoubi Houda , Chentli Farida

Introduction: Cortisol activates lipolysis in adipose tissue resulting in the release of free fatty acids into the circulation, it also activates cholesterol and triglycerides synthesis. The consequence is an increase in total circulating cholesterol and triglycerides with their inherent risks on the cardiovascular system. The aim of our work was to assess the prevalence and characteristics of dyslipidaemia in Cushing’s syndrome (CS).Material and me...

ea0037ep29 | Adrenal cortex | ECE2015

Cushing's syndrome and hypertension

Azzoug Said , Rabehi Leyla , Hannachi Sara , Medjdoubi Houda , Chentli Farida

Introduction: Patients with Cushing’s syndrome (CS) are prone to hypertension as cortisol stimulates renal reabsorption of sodium and enhances vascular sensitivity to catecholamine and angiotensin II. This explains the frequency of hypertension in patients with CS. The aim of our work was to assess the prevalence and characteristics of hypertension in CS.Material and methods: This is a retrospective study concerning 51 CS (44F/7M) in whom we looked ...

ea0037ep1105 | Endocrine tumours | ECE2015

Pituitary apoplexy

Bellarbi Dhiaeddine , Azzoug Said , Rabehi Leyla , Terki Brahim , Chentli Farida

Introduction: Pituitary apoplexy is a rare endocrine emergency characterized by the sudden onset of severe headaches, vomiting, visual abnormalities and pituitary dysfunction secondary to an acute hemorrhage or infarction within a pituitary adenoma.Subjects and methods: We report a retrospective study from 2000 to 2014 of 23 cases with pituitary apoplexy. Their mean age was 38.7±14.8 years, with a male to female ratio of 2:1.R...

ea0035p290 | Clinical case reports Thyroid/Others | ECE2014

46,XX/47,XXY mosaic form of klinfelter syndrome with ambiguous genitalia: a case report

Chabour Fadila , Azzoug Said , Rabehi Leila , Chentli Farida

Klinefelter’s syndrome (KS) is the most frequent form of sex chromosome aneuploidy. The classic form of KS is associated with a 47,XXY karyotype. Mosaic forms of KS are thought to occur in approximately 10% mainly in the form of 46,XX/47,XXY. Other forms of mosaicism are rare among which the 46,XX/47,XXY form is very rare and can manifest as an ambiguous genitalia at birth as reported in our case.A full term child presented at birth an hypospadias w...

ea0035p292 | Clinical case reports Thyroid/Others | ECE2014

Insulinoma and pregnancy: a case report

Saraoui Fatima , Azzoug Said , Rabehi Leila , Chentli Farida

Insulinoma is the most common cause of hypoglycemia related to endogenous hyperinsulinism in adults. It is very rare in pregnancy, fewer than 30 cases of insulinoma presenting in pregnancy have been reported so far and it’s managment is very challenging. We raported here the case of a pregnant women aged 35 years presenting an insulinoma.The diagnosis was made 1 year ago in the presence of hypoglycemia, high levels of inulin and C-peptide and a 10 m...

ea0070aep554 | General Endocrinology | ECE2020

Neurofibromatosis type 1: About two cases

Bouzid Aicha , laloui amina , Meskine Djamila , Azzoug Said

Neurofibromatosis type 1 is a genetic multisystemic disorder involving the skin, the central and peripheral nervous systems, bones, and the cardiovascular and endocrine systems. We report 2 cases of type 1 neurofibromatosis in 2 patients aged 27 and 23 years respectively. The dermatological lesions (neurofibroma and café au lait spots) were the revealing symptoms. Cerebral MRI revealed a glioma of the optic chiasm developing along the Optic nerves. NF1 has been known for ...

ea0070ep277 | General Endocrinology | ECE2020

Glioma of the optic pathways revealed by a nystagmus

Bouzid Aicha , Gasri Salah , Meskine Djamila , Azzoug Said

Abstract: Gliomas of the optic pathways are rare tumors that are mainly seen in children. We report the case of a 4 year old boy followed since the age of 6 months for a nystagmus. It is a boy born at term by vaginal way resulting from parents not consanguineous, the parents noted the nystagmus when their child was 6 months old. After opinion of the ophthalmologist, the child is treated only by optical correction, it is only at the age of 4 years following the installation of ...

ea0032p553 | Endocrine tumours and neoplasia | ECE2013

Prolactinoma and vestibular schwannoma: a very rare association

Chentli Farida , Belhimeur Faiza , Azzoug Said , Fedala Nora Soumeya

Introduction: The occurrence of primary pituitary tumour and cerebral schwannoma in the same person is very rare. Only few cases have been reported so far. The mechanism of this association is still unclear.Aim: Our aim is to report a man with two different brain tumours: a prolactinoma and a cerebellopontine schwannoma in order to discuss the possible mechanism of multiple neoplasms arising in the same person.Case report: A man ag...

ea0029p769 | Endocrine Disruptors | ICEECE2012

Nigella Sativa oil alleviating the reproductive toxicity of chlorpyrifos in male rat

Mosbah R. , Azzoug S. , Haroun N. , Boulakoud M.

Chlorpyrifos (CPF) is a worldwide used organophosphate insecticide for controlling many types of pests in the household, farm and residential settings. It has the potential to negatively affect the reproductive system and fertility. Nigella sativa has been used both as seeds or oil to promote health and fight disease. Hence, the present work was undertaken to evaluate the possible protective role of Nigella sativa oil (NSO) against chlorpyrifos induced reproductive toxicity in...

ea0029p1298 | Paediatric endocrinology | ICEECE2012

Pediatric and adolescent somatotrop adenomas

Chentli F. , Azzoug S. , Belhimer F. , Amani M. , Meskine D.

Introduction: Pituitary somatotrop adenomas are very rare in children and adolescents. They are supposed to be more invasive (invasion of cavernous sinuses or meninges±compression of adjacent neural structures) than adults’ones. We aimed to analyze their characteristics, and their complications.Patients and subjects: are studied subjects whose clinical symptoms began before 20 years old. They all had biological, hormonal, ophthalmological, radi...