Searchable abstracts of presentations at key conferences in endocrinology

ea0014p147 | (1) | ECE2007

Acromegaly due to a lung carcinoid: a case report

malika Rezzoug , Farida Chentli

Acromegaly secondary to a lung carcinoïd is a very rare entity. Secretion of GHRH (Growth hormone releasing hormone) or GHRH like by neuroendocrine tumor induces pituitary hyperplasia and a production of Growth hormone (GH) with or without others anterior pituitary hormones. Total resection of lung tumor induces normalisation of pituitary function as in our observation.AD, 37 years, male, came to our unit for diabetes mellitus and acromegaly. His ch...

ea0011p98 | Clinical case reports | ECE2006

Hypocalcemic cardiomyopathy in a patient with primary hypoparathyroidism and Fahr’s disease

Azzoug S , Chentli F

Hypocalcemic cardiomyopathy due to hypoparathyroidism is a very rare condition which responds favorably to vitaminocalcic treatment.We report the case of a 50 years old man who presented to our unit for general fatigue, apathy and cough lasting several years with a worsening during the last months, there was biological evidence of hypoparathyroidism with profound hypocalcemia (21 mg/l) hyperphosphoremia (53 mg/l) and undetectable PTH levels the CT scan s...

ea0011p655 | Reproduction | ECE2006

Aetiologies of galactorrheas

Chentli F , Meskine D

Galactorrhea (G) is a frequent symptom in endocrinology when breast are systematically examined. In literature there is few works about aetiologies of G. The aim of our work is to evaluate prevalence of G and to study it’s cause in 170 subjects with nipple discharge.Our methodology is based on anamnestic history, clinical exam and a complete hormonal exploration. Women with normal cycle has a temperature curve, endometrial biopsy and progesterone ev...

ea0044ep10 | (1) | SFEBES2016

Pediatric Cushing‘s Syndrome due to primary pigmented nodular adrenocortical disease

Boudiaf Dia Eddine , Chentli Farida

Introduction: Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing’s syndrome in pediatric population. This entity due to genetic mutation has specific histological appearance and can be associated to Carney’s complex and McCune Albright syndrome. Our aim was to report a pediatric case in order to specify clinical and biological characteristics.Case report: A 6 year-old boy with no family or perso...

ea0032p1134 | Thyroid cancer | ECE2013

Brain metastases of papillary thyroid cancer: a case report and literature review

Ahmed-Ali Leila , Chentli Farida

Introduction: Papillary thyroid carcinoma is characterized by a good prognosis and a slow progression. Its metastases are usually located in cervical lymph nodes. But, sometimes they can reach the lung and bones. Cerebral metastases are exceptional as they have been reported in only 4%. Single or multiple, they can be totally symptomatic, but they are life threatening and require specific care as in the following caseCase report: A man aged 56, was refer...

ea0029p124 | Adrenal medulla | ICEECE2012

Incidentally discovered pheochromocytoma (PH)

Kesri N. , Boudiba A. , Chentli F.

The main concern of endocrinologist exploring an adrenal incidentaloma (AI) is the identification of malignant and/or secretant AI leading to rapid cure by removal of the tumor. PH remains one of the most difficult lesions to diagnose. In this study we analyze PH clinic, morphologic and secretory profile. Among a series of 91 AI recruited between 1987 and 2007 having benefited from an adrenal exploration, 56 have been removed and 18/56 were diagnosed as tumors of medullar orig...

ea0029p862 | Endocrine tumours and neoplasia | ICEECE2012

Malignant adrenal incidentaloma

Kesri N. , Boudiba A. , Chentli F.

With the development of medical imaging, many malignant lesions of the adrenal lodge are incidentally discovered. In this prospective monocentric study we are looking for factors of presumption of malignancy in the preoperative stage on a non-oncological series of 91 IS.Monocentric prospective study, AI revealed by TDM±echo supplemented by a clinic/hormonal adrenal exploration ±isotopic. In the absence of against indications, the indication of ...

ea0029p999 | Growth hormone IGF axis - basic | ICEECE2012

Hypertension and cardiovascular risk factors in GH deficiency

Fedala N. , Chentli F. , Haddam A.

Studies showed an increase of cardiovascular risk (CVR) and reduction of the life expectancy observed in the anterior pituitary insufficiency (API) subjects. The morbimortality would be related to GH deficiency not substituted.Aim: To seek the frequency of the hypertension and analyse the predictive factors in subjects with API.A retrospective study relating 55 (47 women, eight men) subjects with API: interrupted pituitarystalk n:6...

ea0011p466 | Endocrine tumours and neoplasia | ECE2006

Diabetic retinopathy in acromegaly

Azzoug S , Adem A , Chentli F

The GH/IGF axis has been implicated in the pathogenesis of retinopathy in diabetic subjects, the aim of this study is to evaluate the prevalence of diabetic retinopathy in hypersomatotropic patients.Subjects and methods: Twenty four hypersomatotropic patients (12 females, 12 males mean age =49 years, mean hypersomatotropic duration =11 years) have diabetes for 7.25 years in average. To search for diabetic retinopathy a funduscopy was performed in all pat...

ea0049ep1267 | Thyroid (non-cancer) | ECE2017

Prevalence of the thyroiditis in childbearing age women

Amani Mohammed El Amine , Chentli Farida

Background and aims: It has been demonstrated that the thyroid autoimmunity, during pregnancy, adversely affects the course of the pregnancy. The anomalies may be prior to the conception, hence the interest of studying the women during the genital activity period. Our objective was to determine the prevalence of the thyroiditis in childbearing age women.Materials and methods: Prospective study, on 270 childbearing age women. Study protocol: clinical exam...