Searchable abstracts of presentations at key conferences in endocrinology

ea0090p799 | Thyroid | ECE2023

Idiopathic Intracranial Hypertension and Grave’s Disease

Zeguir Hadjer , Achir Safia , Arbouche Zakia

Introduction: Idiopathic intracranial hypertension (IIH) is characterized by increased intracranial pressure without a detactable cause. Risk factors for the development of this syndrome are obesity and young female population. IIH due to hyperthyroidism is rare in the literature, mentioned in few individual case reports. The exact mechanism of how hyperthyroidism causes IIH is not known. We are reporting the case of a young women with GravesÂ’ disease presenting with symp...

ea0081p438 | Reproductive and Developmental Endocrinology | ECE2022

Central precocious puberty developed after treatment of leydig cell tumor: case report

Hadjer Bouguerra , Amina Khellaf , Adimi Amel , Arbouche Zakia

Background: Leydig cell tumors (LCTs) are the most prevalent hormone-secreting testicular tumors, but overall, a rare testicular tumor subtype. Surgery is the main therapy with a favorable prognosis. Nevertheless, the development of central precocious puberty after surgery of the tumor has been observed on rare occasions.Case Report: An 8.5-year-old boy presented with symptoms of sexual precocity dating back to 4 years. He had pubic hair (P4), enlarged l...

ea0090p280 | Adrenal and Cardiovascular Endocrinology | ECE2023

Primary hyperparathyroidism and bilateral pheochromocytoma with MAX mutation: Case report

Benabid Chaima , Achir Safia , Nebti Numydia , Arbouche Zakia

Introduction: Pheochromocytomas(PC)are rare catecholamine-producing neuroendocrine tumors. Germline variants of the MYC-associated factor (MAX) gene have been associated with familial PC and paragangliomas (PGL) with an autosomal dominant pattern of inheritance and an overall frequency estimated at 1.9%. Other endocrine and non endocrine tumors can be associated to germline MAX mutations.Case presentation: We report a case of a 37 years old male patient,...

ea0090ep377 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Familial chylomicronemia syndrome: A case report

Seghir Angham , Nebti Numydia , Achir Safia , Arbouche Zakia

Background: Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism with an incidence of one per million in the general population. It is characterized by marked elevation of triglyceride and chylomicron levels, resulting in lipemic plasma and recurrent attacks of acute pancreatitis, eruptive xanthoma, hepatosplenomegaly, and lipemia retinalis.Case Presentation: We report the case of an 18 years old patient, an only son, from a can...

ea0073aep619 | Reproductive and Developmental Endocrinology | ECE2021

Leydig cell tumor in childhood: a case report

Bouguerra Hadjer , Khellaf Amina , Adimi Amel , Arbouche Zakia

BackgroundIn the pediatric population, the Leydig cell testicular tumor (TCL) is rare. It manifests communally in childhood with isosexual precocity gonadotropin-independent due to excess testosterone production.Case reportWe admitted a case of an 8.5 years old boy with the complaint of sexual precocity dating back to 4 years, which manifested by acne, hyper seborrhea, stature advance, penile enlargement, pub...