Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep1064 | Thyroid (non-cancer) | ECE2015

Endocrine involvement in systemic amyloidosis.

Oueslati Ibtissem , Khessairi Nadia , Nacef Ibtissem Ben , Mchirgui Nadia , Khiari Karima , Kaaroud Hayet , Abdallah Nejib Ben

Introduction: Systemic amyloidosis leads to functional compromise of various organs through infiltration of these tissues by amyloid protein.The aim of this study was to determine the endocrine disorders in patients with systemic amyloidosis.Methods: During the period from 1975 to 2006, we collected 580 patients with renal amyloidosis confirmed by histological exam. We selected 123 patients with hormonal exploration. 55 patients ha...

ea0037ep1065 | Thyroid (non-cancer) | ECE2015

Amyloid goitre as the first manifestation of systemic amyloidosis

Oueslati Ibtissem , Hassen Hana Ben Hadj , Nacef Ibtissem Ben , Mchirgui Nadia , Khiari Karima , Abdallah Nejib Ben

Introduction: Thyroid gland may be asymptomatically involved in most patients with secondary systemic amyloidosis. However, clinically detectable amyloid goiter is quite rare; often it is seen in patient with kidney involvement. We report one case of amyloid goitre without kidney manifestation.Case report: A 30-year-old male diagnosed with bilateral bronchiectasis since 1992 was admitted with rapidly growing goiter associated with dysphagia for solids, c...

ea0035p840 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

TSH-secreting pituitary adenomas: a rare cause of hyperthyroidism

Oueslati Ibtissem , Khiari Karima , Mchirgui Nadia , Lakhoua Youssef , Abdallah Nejib Ben

TSH-secreting pituitary tumors (TSH-omas) are a rare cause of hyperthyroidism and account for < 1% of all pituitary adenomas. They are usually benign adenomas arising from a monoclonal expansion of neoplastic thyrotropes.We report two patients’ cases with thyrotropinoma.The first case is a 73-year-old woman, who presents a TSH-secreting pituitary adenoma in the setting of multiple endocrine neoplasia syndrome type 1 (TSH-o...

ea0070aep35 | Adrenal and Cardiovascular Endocrinology | ECE2020

A rare presentation of salt wasting in congenital adrenal hyperplasia with 11β-hydroxylase deficiency.

Belaid Rym , Oueslati Ibtissem , Chehida Anaam Ben , Khessairi Nadia , Yazidi Meriem , Chaker Fatma , Chihaoui Melika

Introduction: Steroid 11β-hydroxylase deficiency (11-OHD) is the second most common causeof congenital adrenal hyperplasia (CAH),characterized by the overproduction of adrenal androgens and deoxycorticosterone (DOC).It usually presents with virilization of the female fetus, precocious puberty in male infants and hypertension with or without hypokalemia in both genders. Because of high levels of mineralocorticoids, patients rarely present with salt wasting (SW). We herein ...

ea0070aep178 | Bone and Calcium | ECE2020

Management of severe hypercalcemia secondary to primary hyperparathyroidism: The efficiency of saline hydration, furosemide, and bisphosphonates.

Mellassi Seifeddine , Oueslati Ibtissem , Belaid Rym , Khessairi Nadia , Yazidi Meriem , Grira Wafa , Chaker Fatma , Chihaoui Melika

Introduction: Severe hypercalcemia is a life-threatening condition which should be managed urgently. Its pharmacological treatment consists of intravenous saline hydration, loop diuretic and intravenous administration of bisphosphonates. However, data evaluating these treatments are very limited.The aim of this study was to assess the efficiency of saline hydration, furosemide, and bisphosphonates in the management of severe hypercalcemia secondary to a ...

ea0070aep637 | Pituitary and Neuroendocrinology | ECE2020

A rare association of hypogonadotropic hypogonadism and GH deficiency in a patient with Addison’s disease

Chatti Hiba-Allah , Oueslati Ibtissem , Yazidi Meriem , Khessairi Nadia , Grira Wafa , Chaker Fatma , Chihaoui Melika

Introduction: Primary adrenal insufficiency is a classically rare but potentially serious disease due to the risk of acute adrenal crisis. Although autoimmune origin is the first etiology in adults, genetic causes are most common in children.Herein, we reporta case of coexisting hypogonadotropic hypogonadism and growth hormone (GH) deficiency in a patient with Addison’s disease.Observation: A 15-year-old boy was referred to o...

ea0070aep714 | Pituitary and Neuroendocrinology | ECE2020

Short stature in turner syndrome: Should we assess growth hormone secretion?

Kamoun Elyes , Oueslati Ibtissem , Chiboub Marwa , Yazidi Meriem , Grira Wafa , Chaker Fatma , Chihaoui Melika

Introduction: Short stature is a common feature in Turner syndrome. It is caused by haplo-insufficiency of the SHOX gene. Growth hormone deficiency does not occur in this disorder as confirmed by the normal GH response to stimulation tests. However, few cases of coexisting GH deficiency and Turner syndrome have been reported. We herein describe two cases of GH deficiency in patient with Turner syndrome.Observation 1: A 20-year-old patient was referred fo...

ea0070aep767 | Pituitary and Neuroendocrinology | ECE2020

Severe hyponatremia revealing hypopituitarism of undetermined etiology

Zargni Asma , Oueslati Ibtissem , Skouri Wafa , Abidi Sahar , Yazidi Meriem , Khessairi Nadia , Chaker Fatma , Chihaoui Melika

Introduction: Hyponatremia represents a frequent electrolyte disorder. It is defined as a serum sodium level below 135 mmol/L and it is severe when serum level is below 125 mmol/l. Endocrine disorders including adrenal deficiency and hypothyroidism are uncommon causes of hyponatremia. Secondary adrenal insufficiency is related with hyponatremia through increased ADH secretion.Herein, we report a case of severe hyponatremia revealing hypopituitarism.<...

ea0070ep34 | Adrenal and Cardiovascular Endocrinology | ECE2020

Clinical, paraclinical features and outcome of adrenocortical carcinoma

Zargni Asma , Oueslati Ibtissem , Abidi Sahar , Khessairi Nadia , Chaker Fatma , Yazidi Meriem , Grira Wafa , Chihaoui Melika

Introduction: Adrenocortical carcinoma (ACC) is a rare aggressive endocrine neoplasm. It’s a heterogeneous malignant tumor with incompletely understood pathogenesis and poor prognosis. The aim of our study was to assess clinical and paraclinical characteristics of ACC and to determine its outcome.Methods: In a retrospective and descriptive study, we included patients with adrenocortical carcinoma confirmed with histopathological examination. Clinic...

ea0070ep147 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Ramadan fasting affects body composition and anthropometric parameters in type 2 diabetic patients.

Boukhayatia Fatma , Oueslati Ibtissem , Cheikh Meriem , Kardi Asma , Chaker Fatma , Yazidi Meriem , Khessairi Nadia , Chihaoui Melika

Introduction: Fasting the month of Ramadan is practiced by more than one billion Muslims worldwide, including type 2 diabetic patients. Its effects on body composition and body weight in type 2 diabetic patients are controversial.The objective of our study was to assess the evolution of anthropometric parameters as well as the body composition in type 2 diabetic patients who fasted the month of Ramadan.Methods: We conducted a prosp...