Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep758 | Pituitary and Neuroendocrinology | ECE2022

Severe growth retardation due to pituitary stalk agenesis: a case report

Rifai Kaoutar , Azriouil Manale , Kamel Farah , Elmoatamid Kaoutar , Guissi Loubna , Iraqi Hinde , Gharbi Mohamed Elhassan

Introduction: Growth retardation is considered severe when the height of the child is -3 standard deviation (SD) below the average height in reference to the growth curves of children of the same sex and age. Pituitary stalk interruption syndrome (PSIS) is one of the most common conditions in children with short stature.Case report: We report the case of a 12-years old boy with no clinical history of perinatal injury or traumatic birth, who was admitted ...

ea0090ep36 | Adrenal and Cardiovascular Endocrinology | ECE2023

Adrenal incidentaloma revealing a cystic pheochromocytoma

Dounia Talbi , Zakaria Cheibete , Elmoatamid Kaoutar , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Pheochromocytomas are rare neuroendocrine tumors producing catecholamines, they are usually unilateral. However, they can be located bilaterally. They still pose several problems in their diagnosis if they are associated with an adrenal cyst, which is the case in our patient.Case Report: A 34-years-old male patient, his medical and family histories were non specific, admitted to the emergency room for lumbar pain, with no other associated s...

ea0090ep498 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Stiff person syndrome revealing a LADA

Dounia Talbi , Elmoatamid Kaoutar , Amira Ikram , Azriouil Manal , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Stiff-Person Syndrome (SPS) is a rare autoimmune neurological disorder that can be associated with other autoimmune diseases including type 1 diabetes mellitus (T1DM). The presence of alternative forms of autoimmune diabetes, such as latent autoimmune diabetes in adults (LADA) in SPS, is not well described.Case Report: A 63 years old male patient, his medical and family histories were non-specific. He developed progressive rigidity in trunc...

ea0099ep913 | Pituitary and Neuroendocrinology | ECE2024

HTA and hypokalemia: always think of cushing’s disease

Dounia Talbi , Kaoutar Elmoatamid , Ghizlane Sebbar , Kaoutar Rifai , Hinde Iraqi , Mohamed El Hassan Gharbi

Introduction: Arterial hypertension of endocrine origin remains a rare and curable cause of hypertension. The association of hypertension and hypokalemia should always prompt us to consider cushing’s disease.Case Report: A 39-year-old female patient, followed for 9 years for hypertension on dual therapy. Clinical examination was unremarkable, in whom the diagnosis of ACTH-dependent cushing’s syndrome was made on the basis of clinical and biolog...

ea0099ep1272 | Late Breaking | ECE2024

Dilated cardiomyopathy: an unusual revelation of autoimmune hypothyroidism; case report

Qasdi Ikrame , Ouirar Hasna , Elmoatamid Kaoutar , Toulali Fatima , Rifai Kaoutar , Hinde Iraqi , Elhassan Gharbi Mohamed

Introduction: The occurrence of Dilated Cardiomyopathy (DCM) and hypothyroidism induced systolic dysfunction is rare, especially when it presents as an initial manifestation of hypothyroidism Case We report the case of a 57-year-old patient, a known chronic smoker, who was admitted to the emergency department reporting asthenia, NYHA class III dyspnea, cardiac angina, and periorbital oedema. The ECG reveals a regular rhythm at 50 bpm and diffuse low voltage with firstdegree at...

ea0099ep1309 | Late Breaking | ECE2024

Malignant pheochromocytoma unmasked by paralyzing sciatic symptoms: a case report

Ouirar Hasna , Zouna Caimae , Qasdi Ikrame , Elmoatamid Kaoutar , Toulali Fatima , Sabbar Ghizlane , Rifai Kaoutar , Hinde Iraqi , Elhassan Gharbi Mohamed

Introduction: Developing in the adrenal medulla’s chromaffin cells, pheochromocytoma (PC) is an infrequent tumor Illustrating the instance of a patient diagnosed with malignant adrenal pheochromocytoma (PCM) following the onset of paralyzing sciatic painCase: A 60-year-old patient managing hypertension with triple therapy and type 2 diabetes using metformin and insulin glargine. The patient sought emergency care due to recurrent and disabling sciati...

ea0099p407 | Late-Breaking | ECE2024

Schmidt’s syndrome: think about it in males too: A case report

Ouirar Hasna , Qasdi Ikrame , zouna Caimae , Meryem Karimi , Azagouagh Hajar , Elmoatamid Kaoutar , Toulali Fatima , Sabbar Ghizlane , Rifai Kaoutar , Hinde Iraqi , Elhassan Gharbi Mohamed

Introduction: Autoimmune polyendocrine syndrome type 2 is a rare autosomal dominant life-threatening syndrome. It is defined by the presence of Addison’s disease in combination with at least one of the known autoimmune diseases: thyroid autoimmune disease, type 1 diabetes, and hypogonadism. The coexistence of Addison’s disease and autoimmune thyroid disease has been known as Schmidt’s syndrome. We are detailing the case of a patient who exhibited this syndrome a...

ea0099ep1273 | Late Breaking | ECE2024

When an ectopic and hyperfunctional thyroid nodule appears 2 decades after subtotal thyroidectomy: A case report

Ouirar Hasna , Qasdi Ikrame , Zouna Caimae , Riad Amal , Elmoatamid Kaoutar , Toulali Fatima , Sabbar Ghizlane , Rifai Kaoutar , Hinde Iraqi , Elhassan Gharbi Mohamed

Introduction: A toxic thyroid nodule refers to a nodule that functions autonomously, causing an overabundance of thyroid hormones. It is generally considered non-malignant. Making a decision regarding surgery in hyperthyroid patients necessitates the accurate localization of the toxic region. Here we report a case of an intrathoracic toxic thyroid nodule causing hyperthyroidism with a normally functioning cervical thyroid nodule.Case: A 63 year-old femal...