Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep733 | Pituitary and Neuroendocrinology | ECE2023

Endogenous hyperinsulinemic hypoglycemia: A retrospective analysis of 10 cases

Belabed Wafa , Mnif Fatma , Missaoui Abdel Mouhaymen , Elleuch Mouna , Charfi Nadia , Mejdoub Nabila , Mnif Mouna , Abid Mohamed

Background and aim: Non-diabetic hypoglycemia is a rare entity that regroups several pathologies. Its exact diagnosis is mostly challenging. Endogenous hyperinsulinism is a curable cause that should be thoroughly screened. The objective of our study was to analyze the ethipathological aspects of hypoglycemia by endogenous hyperinsulinism.Patients and methods: We conducted a retrospective study at the Endocrinology department of Hedi Chaker University Hos...

ea0090ep855 | Pituitary and Neuroendocrinology | ECE2023

Risk of neoplasms in acromegaly : a monocentric retrospective study

Haj Kacem Akid Faten , Belabed Wafa , Mouhaymen Missaoui Abdel , Charfi Nadia , Mejdoub Nabila , Ben Salah Dhoha , Abid Mohamed

Background and aim: Acromegaly is a rare condition caused by an excessive secretion of growth hormone (GH) and insulin-like growth factor1 (IGF-1), which are responsible for exaggerated somatic growth, cardiometabolic disturbances and an increased neoplastic risk. This study aims to assess the tumorigenic potential of GH excessive secretion.Patients and Methods: We conducted a retrospective study (1997-2020) at the Endocrinology department of Hedi Chaker...

ea0063p834 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Familial multiple endocrine neoplasia type 1 revealed by a maxillary swelling

Salah Dhouha Ben , Gargouri Imen , Mnif Fatma , Elleuch Mouna , Charfi Nadia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder caused by mutations in the MEN1 tumor suppressor gene and is characterized clinically by tumors in two or more endocrine glands, such as the pituitary gland, parathyroid glands or pancreatic islets. We describe an atypical presentation of familial hyperparathyroidism evoking the diagnosis of MEN1 in the first place.Observations: We report a three-member family....

ea0049ep77 | Adrenal cortex (to include Cushing's) | ECE2017

Malignant androgen-secreting adrenocortical carcinoma with adrenal insufficiency: a case report

Mnif Fatma , Kalthoum Mehdi , Elleuch Mona , Wajdi Saafi , Charfi Nadia , Ammar Mouna , Feki Hamza , Mnif Mona , Abid Mohamed

Adrenocortical carcinoma (ACC) is a rare malignancy, accounting for 0.02% of all annual cancer. The majority of these tumors are benign, non-functioning adenomas that are incidentally discovered on abdominal image studies. Others are functional adenomas secreting cortisol, aldosterone, or less commonly androgens or estrogens. Pure androgen-secreting adrenal tumors are very rare.Case report: A 34-year-old female patient presented with pain in the left upp...

ea0049ep167 | Endocrine tumours and neoplasia | ECE2017

Corticotroph deficiency in patients with insulinoma

Kacem Faten Hadj , Ammar Mouna , Elleuch Mouna , ghorbel Dorra , Abdallah Rihab Ben , Charfi Nadia , Sefi Wajdi , Mnif Mouna , Abid Mohamed

Introduction: The metabolic stressor, hypoglycemia, elicits integrated counterregulatory responses, including activation of the hypothalamic–pituitary–adrenal axis. However, it is suggested that recurring insulin-induced hypoglycemia can impair this counter-regulation. Here we report three cases of patients with isulinoma and corticotroph deficiency.Case reports: The first case, 38-year-old man was referred because of recurrent episode...

ea0049ep189 | Endocrine tumours and neoplasia | ECE2017

An unknown giant neuroendocrine tumor

Rekik Nabila , Ghorbel Dorra , Mnif Fatma , Kalthoum Mahdi , Mrabet Houcem , Charfi Nadia , Elfekih Hamza , Mnif Mouna , Abid Mohamed

Introduction: Neuroendocrine tumors may develop in almost any organ. These types of tumors may present with giant and asymptomatic mass. We describe a case of a large non functional neuroendocrine tumor reported in the department of endocrinology and diabetology of Hedi Chaker hospital in Sfax-Tunisia in 2016.Presentation of case: A 28 years old male presented with asthenia, gastric heaviness and epigastric pain. Further computerized tomography, a large ...

ea0049ep1128 | Female Reproduction | ECE2017

Secondary amenorrhea after bone marrow transplantation and adjuvant chemotherapy misdiagnosed as disorder of sex development: a case report

Elleuch Mouna , Ammar Mouna , Kacem Faten Hadj , Ghorbel Dorra , Rekik Nabila , Charfi Nadia , Kalthoum Mahdi , Mnif Mouna , Abid Mohamed

Introduction: Disorders of sex development (DSD) is a congenital condition in which the development of chromosomal, gonadal or genital sex is atypical. A female appearance patient with secondary amenorrhea and 46 XY karyotype seems to be solid evidences to diagnose Y-chromosome-related DSD diseases, while it is not necessarily the accurate diagnosis. We here report a case of a 16- year-old girl with secondary amenorrhea and 46 XY karyotype after bone marrow transplantation (BM...

ea0049ep1349 | Thyroid (non-cancer) | ECE2017

Lymphoid hyperplasia in Graves’ disease: about 2 cases

Hadjkacem Faten , Ghorbel Dorra , Mnif Fatma , Elfekih Hamza , Rekik Nabila , Mrabet Houcem , Ammar Mouna , Charfi Nadia , Abid Mohamed

Introduction: Graves’ disease GD is an autoimmune disease, which can manifest with a variety of extrathyroidal clinical syndromes. Though quite rare, this disease can also manifest with lymphoid hyperplasia.Case report: Two cases are reported in the department of endocrinology and diabetology of Hedi Chaker hospital in Sfax-Tunisia from 2006 to 2016 associated GD with lymphoid hyperplasia reaction. The first case was a 32 years old male with history...

ea0037ep85 | Adrenal cortex | ECE2015

Subclinical Cushing's syndrome: report of 17 cases

Kacem Faten Haj , Cheikhrouhou Nesrine , Charfi Nadia , Lassoued Najwa , Mnif Fatma , Mnif Mouna , Rkik Nabila , Abid Mohamed

Introduction: Subclinical Cushing’s syndrome refers to autonomous cortisol secretion in patients who do not have the typical signs and symptoms of hypercortisolism. This study was undertaken to describe clinical, biological and radiological features of this disease and to evaluate the clinical outcome after surgical and medical treatment.Methods: Retrospective study conducted over a period of 12 years and including 17 patients hospitalised in our de...

ea0037ep534 | Diabetes (complications & therapy) | ECE2015

Diabetic foot infection: study of 109 patients

Kacem Faten Hadj , Ammar Mouna , Charfi Nadia , Cheikrouhou Nesrine , Mnif Fatma , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Diabetic foot infection (DFI) is a major public health problem, both for its morbid clinical consequences mainly ulcers and the economic social cost due to repeated hospitalisations and the high rate of amputation.Objectives: Analyse the clinical presentation of DFI, study risk factors of developing this infection and describe the therapeutic management.Materials and methods: Retrospective study spread over 8 years ol...