Searchable abstracts of presentations at key conferences in endocrinology

ea0029p267 | Calcium & Vitamin D metabolism | ICEECE2012

Vitamin D status in primary hyperparathyroidism

Yazidi M. , Kammoun I. , Ben Said R. , Gharsallah G. , Haouet E. , Turki Z. , Ben Slama C.

Vitamin D deficiency seems to be more prevalent in patients with primary hyperparathyroidism (PHPT) than in general population. This association has many clinical and therapeutic implications.The aim of this study was to assess the vitamin D status of patients with PHPT and to describe the clinical presentation of the disease when vitamin D deficiency is associated.Methods: We studied in a retrospective manner, the case of seven pa...

ea0029p884 | Endocrine tumours and neoplasia | ICEECE2012

Special diagnostic, therapeutic and evolutive aspects of insulinoma: a tunisian experience

Oueslati I. , Kammoun I. , Riahi T. , Ouannes S. , Kandara H. , Turki Z. , Ben Slama C.

Insulinoma is a very rare type of islet cell tumor. The aim of our study is to report our clinical experience with insulinoma in order to determine clinical, biological, radiological and therapeutic particularities of this tumor type.It’s a retrospective study, including five patients (three women and two men) referred to our department between 2005 and 2011 for hypoglycemia exploration. Mean age of our group is 39.8±15.4 years (ranges: 20&#150...

ea0029p1512 | Pituitary Clinical | ICEECE2012

Sleep apnoea syndrome in acromegaly

Khemiri H. , Turki Z. , Yazidi M. , Kammoun I. , Turki M. , Ben Salem L. , Ben Slama C.

Sleep apnoea syndrome (SAS) is common in acromegaly and both diseases are independently associated with hypertension and insulin resistance contributing to increased morbidity and mortality.The aim of this study was to assess the prevalence and risk factors of SAS in acromegaly, to study clinical and polysomnographic particularities of SAS in acromegaly and to analyze the effects of acromegaly treatment on SAS.It’s a retrospec...

ea0011p659 | Reproduction | ECE2006

Clinical, hormonal, neuroradiological characteristics and response to treatment in 29 macroprolactinomas

Bouguerra R , Ben Salem L , Turki Z , Smida H , Kammoun I , Saidi Ch , Ben Slama C

Most macroprolactinomas are responsive to dopamine against drugs. Bromocriptine (BRC) has been available and extensively used in our country. The aims are to assess the outcome in 29 patients with macroprolactinomas who were treated with BRC.Material and methods: A multicentric study of 29 patients with macroprolactinoma (19 female; 10 males). The mean age was 33 years. The pituitary mass was larger than 10 mm in diameter. There was no endocrinological e...

ea0056p144 | Female Reproduction | ECE2018

Female fertility in congenital adrenal hyperplasia

Gargouri Imen , Mnif Fatma , Ajili Rihab , Hadjkacem Faten , Sessi Salwa , Kammoun Mahdi , Mnif Mouna , Abid Mohamed

Introduction: Congenital adrenal hyperplasia (CAH) is a genetic disease with autosomal recessive inheritance. The deficit in 21-hydroxylase (21-OH) is by far the most common enzyme deficiency CAH, since it represents 95% of the cases. Fertility in wome is found to be reduced due to hormonal, mechanical and psychological factors.Patients and methods: It is about a descriptive and prospective study conducted in 15 patients collected in the endocrinology de...

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...

ea0073aep709 | Thyroid | ECE2021

Antithyroid drugs as treatment of neutropenia in hyperthyroidism

Essayeh Sawsen , Jemel Manel , Chatti Hiba , Madhi Wiem , Gharbi Radhouane , Kandara Hajer , Kammoun Ines

IntroductionHematological abnormalities are frequently observed in hyperthyroidism and are part of complex, multifactorial pathogenetic mechanisms that are still poorly understood, which can affect the three hematopoietic lineages in isolation or in combination. For the endocrinologist, they raise the issue of the risk of their aggravation under the hamatotoxic effect of antithyroid drugs (ATDs).Case presentation<p class="abste...