Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep104 | Adrenal and Cardiovascular Endocrinology | ECE2023

When pheochromocytoma occurs in the elderly: A case report

Toulali Fatima , El Hafiani Asmae , Echchad Lamya , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Pheochromocytoma is a rare neuroendocrine tumor. It is usually diagnosed in subjects between 40 and 50 years of age. The occurrence of pheochromocytoma in the elderly is much rarer and has its own particularities. We report the case of a 70-year-old female patient with invasive pheochromocytoma.Case presentation: A 70-year-old female patient with a history type 2 diabetes for 18 years on oral antidiabetics and insulin. The history of his di...

ea0090ep222 | Calcium and Bone | ECE2023

Femoral fracture revealing primary hyperparathyroidism in a very young patient and multiple lytic bone lesions: A case report

El Hafiani Asmae , Gharbi Mohamedelhassan , Hinde Iraqi , Kaoutar Rifai , Fatima Toulali , Hamza Elqandili

Introduction: Primary hyperparathyroidism is the most common endocrinopathy after diabetes and thyroid diseases. Most often, the diagnosis is made at the asymptomatic stage due to the frequent phosphocalcic assessment objectifying hypercalcemia. Much more rarely, primary hyperparathyroidism is diagnosed at the stage of digestive, renal or bone complications. We report the case of a young patient with a femoral fracture that revealed primary hyperparathyroidism.<p class="ab...

ea0090ep537 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Keto-acidosis decompensation and centropontic myelinolysis: incidental finding-a case report

El Hafiani Asmae , Hinde Iraqi , Gharbi Mohamedelhassan , Kaoutar Rifai , Fatima Toulali , Soukaina El Harouni

Introduction: Centropontic myelinolysis (CPM) is a neurological pathology related to axonal demyelination lesions, often localized at the pontine level. For a long time, this condition was attributed to rapid correction of hyponatremia. A few cases of PCM with normal natraemia have been described, in a context of undernutrition, chronic alcoholism, hypokalaemia or hyperglycaemia.Patient and observation: We report the case of an 18 years old patient, type...

ea0090ep819 | Pituitary and Neuroendocrinology | ECE2023

Noonan syndrome associated with SOS1 gene mutation with autosomal dominant RASopathy : a case report

El Hafiani Asmae , Azriouil Manal , Echchad Lamya , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Noonan syndrome (NS) is an autosomal dominant genetic disorder characterized by the combination of facial dysmorphia, short stature and congenital heart disease. The mutation of the PTPN11 gene is present in 50% of cases, recently the mutation of other genes was found, notably KRAS and SOS1. We report the case of a patient followed in our department for NS with a SOS1 gene mutation.Case report: A 4 years old male patient, referred to our de...

ea0090ep1023 | Thyroid | ECE2023

Association of Basedow and primary biliary cholangitis : a case report

El Hafiani Asmae , Hinde Iraqi , Gharbi Mohamedelhassan , Kaoutar Rifai , Meryem Karimi , Fatima Toulali

Introduction: Primary biliary cholangitis (PBC) is a rare chronic cholestatic liver disease, which is most likely of autoimmune origin. It is often associated with other autoimmune diseases, although it is rarely seen with Basedow.Observation: We report the case of a 38 years old patient, chronic smoker, who presents clinical and biological hyperthyroidism related to Basedow, treated with synthetic antithyroid drugs for years with poor compliance and not...