Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep640 | Growth hormone IGF axis - basic | ECE2017

Insulin resistance and acromegaly: about 15 cases

Nawal El Ansari , Askaoui Sara

Contexte: Acromegaly is a rare disease, usually caused by hypersecretion of growth hormone (GH) by a pituitary adenoma and very rarely by ectopic secretion of GHRH. It remains a serious disease reduces life expectancy because of its cardiovascular and metabolic impact.Objective: The objective of this study is to report the glycemic profile in patients followed for acromegaly in the endocrinologic center of CHU Med VI of Marrakech.P...

ea0049ep888 | Male Reproduction | ECE2017

Delayed puberty revealing an uncommon genetic disease: about one case

Nawal El Ansari , Askaoui Sara

Contexte: Kallmann syndrome is a rare genetic disease which can affect both men and women. It combines hypogonadotropic hypogonadism which characterised by a failure to start or to fully complete puberty naturally; olfactory disorders such hyposmia or anosmia, impaired color vision, deafness, unilateral or bilateral renal aplasia and midline anomalies.Objective: We report a case of this rare syndrome, responsible of delayed puberty view of infertility.</...

ea0063p231 | Pituitary and Neuroendocrinology 1 | ECE2019

Growth hormone deficiency, which etiologies?

Askaoui Sara , Elmghari Guizlane , El Ansari Nawal

Introduction: Growth hormone deficiency is a rare cause of stunting; its diagnosis is often delayed by severe growth retardation; confirmed by non-response to GH stimulation tests (insulin and glucagon-propranolol test). The absence of early diagnosis and treatment can lead to severe growth retardation. We propose to determine the prevalence of different etiologies of growth hormone deficiency in patients followed for a saturo-weight delay at the Arrazi Hospital, Medical Unive...

ea0063p893 | Diabetes, Obesity and Metabolism 3 | ECE2019

Necrosis of the nasal pyramid in a type 1 diabetic after prolonged intubation: in the light of a case

Askaoui Sara , Lmghari Guizlane , Ansari Nawal El

Introduction: Necrosis of the nasal pyramid is mainly of traumatic origin, among the other possible causes, those induced by systemic diseases, in particular Wegener’s granulomatosis…We report a case of necrosis of the nasal pyramid secondary to prolonged intubation in a type 1 diabetic.Observation: Patient T.T, 28 years old, followed for a poorly balanced type 1 diabetes, admitted to a blood clot in a table of diabetic ketoacidosis. The patie...

ea0063ep1 | Adrenal and Neuroendocrine Tumours | ECE2019

Pheochromocytoma in the setting of a neurofibromatous type 1

Askaoui Sara , Lmghari Guizlane , El Ansari Nawal

Introduction: Neurofibromatosis type 1 (NF1) is the most common autosomal dominant disease. The endocrine manifestations of NF1 are represented by pubertal abnormalities and pheochromocytoma. We report a case.Observation: Mr. G.A, age 28, consulling for a grade 2 HTA evolving for 3 years. The anamnesis notes paroxysmal crises made of Ménard triad. The exam notes a correct blood pressure, 18 coffee latte tasks, lentiginous tasks. Two neurofibromas of...

ea0063p72 | Calcium and Bone 1 | ECE2019

Severe hypocalcemia: when the skin expresses itself

Askaoui Sara , Lmghari Guizlane , Rafi Sana , Ansari Nawal El

Introduction: Impetigo herpetiformis is a rare dermatological disorder, mimicking generalized pustular psoriasis. It is characterized by a generalized erythema-pustular eruption accompanied by fever. Its etiopathogenesis is poorly coded but triggers have been identified such as hypocalcemia in more than half of cases and pregnancy. We report a case of severe hypocalcemia secondary to hypoparathyroidism revealed by impetigo herpetiformis.Case report: Fort...

ea0063p146 | Diabetes, Obesity and Metabolism 1 | ECE2019

Metabolic profile and diabetes in prison

Askaoui Sara , Oukit Loubna , Lmghari Guizlane , El Ansari Nawal

Introduction: The prison environment is a space that involves certain restrictions on prisoners. The diabetic subject requires, however, special attention. The aim of this work is to evaluate the impact of this medium on the glycemic balance and the metabolic profile.Patients and method: Descriptive cross-sectional study carried out on a health campaign day in a penitentiary center, in the men’s sector, and concerned patients with known diabetes fro...

ea0063p232 | Pituitary and Neuroendocrinology 1 | ECE2019

Mammosomatotropic adenoma and acromegaly: about 3 cases

Askaoui Sara , El Mghari Guizlane , Raiss Hanane , El Ansari Nawal

Introduction: Somatotropic adenomas are clinically expressed either by acromegaly or by gigantism according to age of onset. Several histological types are involved. Immunohistochemistry provides conclusive evidence that significant diversity exists between growth hormone secreting (GH) tumors in excess. We report three observations of a particular histological type: mammosomatotropic adenoma.Observation 1: Mrs. M.H., aged 56, hypertensive for 10 years, ...

ea0063p233 | Pituitary and Neuroendocrinology 1 | ECE2019

Silent somatotropic adenoma: about a case

Askaoui Sara , Lmghari Guizlane , Rafi Sana , El Ansari Nawal

Introduction: Somatotropic adenomas are classically a source of hypersecretion of GH and consequently of IGF1 responsible for the clinical signs of acromegaly. Rarely, these adenomas remain ‘silent’, without any obvious clinical manifestation. They can then be detected on the basis of a routine determination of growth hormone under oral glucose tolerance test (GH/OGTT) and insulin growth factor 1 (IGF1) or be diagnosed only to immunohistochemical study as is the case...

ea0063p348 | Thyroid 1 | ECE2019

Thyroid angiosarcoma: in the light of a case

Askaoui Sara , Lmghari Guizlane , Rafi Sana , Ansari Nawal El

Introduction: Angiosarcoma is a highly malignant tumor, very rare and even more so when it comes to a thyroid localization. It is characterized morphologically by its vascular differentiation and cytological polymorphism. The objective of this study is to report a case of this entity with its evolution in the postoperative period.Observation: patient of 54-year-oldm, with no pathological history. Operated (total thyroidectomy) for compressive multihetero...