Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep412 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

An inaugural diabetic ketoacidosis revealed by odontogenic facial cellulitis

Boukhalfa Ahmed , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Odontogenic facial cellulitis (OFC) is a soft cellulo fatty tissue infection of lesser resistance in different spaces, delimited by the musculoaponeurotic insertions on the maxillary and mandibular bone cortices. when patients have underlying diseases such as diabetes mellitus (DM) or cancer, compromised immune systems may lead to the opportunistic progression of seemingly minor infections. We report the case of a patient who presented an inaugural diabetic ketoa...

ea0099ep1223 | Adrenal and Cardiovascular Endocrinology | ECE2024

Primary aldosteronism: clinical presentation and management about 2 cases

Boukhalfa Ahmed , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Primary aldosteronism (PA) is widely recognized as the most common form of secondary hypertension (1). PA, also known as Conn syndrome, is a group of pathological conditions associated with an aldosterone secretion inappropriate for sodium intake, that is relatively autonomous from renin–angiotensin system activity and potassium levels.Clinical Case 1: Thirty two year-old patient, diagnosed since 11 months with arterial hypertension wi...

ea0099ep1123 | Endocrine-Related Cancer | ECE2024

Abdominal paraganglioma: diagnostic and therapeutic challenge! about 2 cases

Boukhalfa Ahmed , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Paragangliomas (PGL) are rare neuroendocrine tumors of the chromaffin cells of the sympathic and parasympathic ganglia. They are responsible for catecholaminergic hypersecretion syndrome. Clinical presentation and malignant potential are variable and closely linked to the genetic profile.Clinical Case 1: Fifty three year old patient, diagnosed with diabetes and high blood pression for 4 years, she reported a Menard’s Triad evolving for...

ea0099ep903 | Pituitary and Neuroendocrinology | ECE2024

Craniopharyngioma in children: a therapeutic challenge! (about 2 cases)

Boukhalfa Ahmed , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Craniopharyngioma (CP) is a rare epithelial tumor of the sellar and suprasellar region, histologically of low grade (WHO grade I). Significant locoregional invasion explains the frequency of recurrence, mainly due to incomplete surgical resection. We report two cases of craniopharyngioma in children, in order to outline the therapeutic difficulties encountered during management.Case 1: Eleven years-old patient reported frontal headache with...

ea0099ep245 | Thyroid | ECE2024

Thyroid storm: One major endocrine emergency revealing another !!

Boukhalfa Ahmed , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Thyroid storm (TS) is a severe manifestation of thyrotoxicosis, (1). It is most commonly seen in Graves’ disease and can occur due to a non-compliance to anti-thyroid medications Management includes both addressing end organ damage and attaining a euthyroid state. We report the case of a patient who presented a thyroid storm complicating a grave’s disease and unmasking, during its management, a corticotropic insufficiency.Clinical...

ea0081ep592 | Endocrine-Related Cancer | ECE2022

Pheochromocytoma associated with type 1 neurofibromatosis

Sara Chtioui , Boukhalfa Ahmed , Sanaa Rafi , Mghari Ghizlane EL , Ansari Nawal EL

Introduction: Compared to normal population, patients with neurofibromatosis are at higher risk for the development of benign and malignant tumors. Pheochromocytomas are relatively rare in neurofibromatosis type 1 (NF1), and malignant ones are even rarer.Aim of the presentation: Our aim was to report a malignant pheochromocytoma with multiple metastases in a patient with NF1.Case report: A male patient aged 23 years old, with lapar...

ea0081ep1167 | Late Breaking | ECE2022

Silent giant pheochromocytoma : about a rare entity

Sara Chtioui , Boukhalfa Ahmed , Sanaa Rafi , Ghizlane El Mghari , Nawal El Ansari

Introduction: Pheochromocytomas are catecholamine producing tumors which arise from chromaffin cells within the adrenal medulla. Silent pheochromocytomas are rare entities that do not present with the classical symptoms commonly seen in catecholamine-secreting tumors. Case report: We report a case of 70-year-old-woman patient who presented with left sided abdominal pain and discomfort for 6 months. A preoperative Computed tomography (CT) scan showed a hu...

ea0090ep74 | Adrenal and Cardiovascular Endocrinology | ECE2023

Malignant pheochromocytoma : A therapeutic challenge !

Sara Chtioui , Boukhalfa Ahmed , Rafi Sana , Tabib Ghizlane El Mghari , El Ansari Nawal

Introduction: Pheochromocytomas are rare catecholamine-producing neuroendocrine tumors that are usually benign, but which may also present as or develop into a malignancy. Predicting such behavior is notoriously difficult and there are currently no curative treatments for malignant tumors.Case Report: A male patient aged 23 years old who was investigated for headaches, flushing and palpitations. The patient presented with classic clinical features of NF-...

ea0090ep427 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Autoantibody-negative insulin-dependent diabetes mellitus after COVID 19: Case report

Ismail Zahra , Boukhalfa Ahmed , Rafi Sana , Mghari Ghizlane El , El Ansari Nawal

Introduction: The COVID pandemic was a challenge in terms of physiopathology and therapeutics. Diabetics represent more than 40% of patients hospitalized for COVID. There was many new cases of diabetes declared during or after a COVID. The purpose of this report is to raise the link between Sars-Cov-2 infection and the appearance of glycemic disorders and new cases of diabetes.Case Presentation 1: A 28-years-old man who had a serious COVID-19 a month ago...

ea0090ep530 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Diabetic osteoarthropathy: A case report

Boukhalfa Ahmed , Ismail Zahra , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Diabetic osteoarthropathy (D.O) commonly referred to as Charcot’s foot is a complication secondary to neuropathic and inflammatory osteolysis, occurring in a setting of old and/or poorly controlled diabetes. Its pathophysiology remains poorly understood and its diagnosis must be systematically evoked in the presence of any inflammatory sign that localised to the foot or ankle occurring on a background of diabetic neuropathy.Clinical ca...