Searchable abstracts of presentations at key conferences in endocrinology

ea0073ep118 | Diabetes, Obesity, Metabolism and Nutrition | ECE2021

The traditionnel bath: it’s time to put an end to this dangerous ritual for diabetics!

Ijdda Sara , Joel Rudy Ekondzoula , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

IntroductionIn Morocco, the Moorish bath is an important social ritual. All categories of society frequent it very regularly. The traditionnel bath can lead in the diabetic, by the means of acute decompensations, serious falls and burns, with heavy functional, social and psychological consequences. Through this observation, we report the risks associated with the Moorish bath, and we underline the value of educating diabetic patients and making them awar...

ea0073ep212 | Thyroid | ECE2021

Ectopic thyroid tissue: about 2 cases

Sara Chtioui , Sanaa Bammou , Sanaa Rafi , Mghari Ghizlane El , Ansari Nawal El

IntroductionAccessory thyroid is defined as the presence of thyroid tissue in locations other than the normal anterior neck region between the second and fourth tracheal cartilages. It is a congenital disease caused by the abnormal migration of thyroid tissue in the embryonic stage. Lingual thyroid is the most common form of ectopic thyroid, extra lingual thyroid tissue is commonly located in the anterior cervical area, along the path of the thyroglossal...

ea0099ep89 | Adrenal and Cardiovascular Endocrinology | ECE2024

Pheochromocytoma associated with pregnancy. Diagnostic difficulties and management

Ismail Zahra , ibrahim Fod moustapha , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Pheochromocytoma is a rare cause of hypertension in pregnancy. Its prevalence ranges from 0.2% to 0.002% of cases of hypertension in pregnancy. Early diagnosis and appropriate management can reduce mortality and morbidity. Were report a case of pheochromocytoma diagnosed during pregnancy.Observation: 34-year-old diabetic patient, 29 weeks pregnant. Admitted for hypertensive peaks up to 170 mmHg of systolic, initially mistaken for pre-eclamp...

ea0099ep294 | Adrenal and Cardiovascular Endocrinology | ECE2024

Jaw Tumor syndrome revealing hyperparathyroidism: about a case report

Hassan Neima , Ouakrim Hind , Rafi Sana , Mghari Ghizlane El , El Ansari Nawal

Introduction: Hyperparathyroidism is a common medical condition, but in 5-10% of cases, it is part of Jaw Tumor syndrome, an autosomal dominant syndrome linked to a mutation in the HRPT2 gene. This syndrome is characterized by the presence of mandibular brown tumors and primary hyperparathyroidism.Case report: A 24-year-old patient with a history of severe chronic renal failure in the left single kidney, presenting ureterohydronephrosis, underwent mandib...

ea0099ep296 | Adrenal and Cardiovascular Endocrinology | ECE2024

Adrenal insufficiency due to adrenal involvement in non-hodgkin’s lymphoma

Ait Si Ali Zineb , oussama jaddi , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: The non-Hodgkin lymphomas (NHL) involve extralymphatic sites more often than does Hodgkin lymphoma; consequently, tumor involvement of almost every abdominal organ has been recorded. Adrenal involvement in patients with NHL may be present at the time of initial assessment. however, adrenal insufficiency as a consequence of adrenal invasion is rare. We report a case of a patient diagnosed with NHL with breast and bilateral adrenal involvement.<p class="abstext...

ea0099ep416 | Adrenal and Cardiovascular Endocrinology | ECE2024

Idiopathic unilateral genycomastia in a child

Hassan Neima , Ouakrim Hind , Rafi Sana , Mghari Ghizlane El , El Ansari Nawal

Introduction: Gynecomastia, marked by mammary gland hypertrophy, arises from an imbalance between androgens and estrogens. Notable etiologies include hypogonadism, tumors, iatrogenic causes, and idiopathic factors.A case report: A patient aged 8 years and 10 months, with no pathological history, was admitted for further management of right unilateral gynecomastia. The functional signs included unilateral right hypertrophy in the retroareolar region. On p...

ea0099ep1095 | Adrenal and Cardiovascular Endocrinology | ECE2024

Adrenal insufficiency revealing multifocal tuberculosis

Alahyane Meryam , Rafi Sana , Bari Manar , El Mghari Ghizlane , El Ansari Nawal

Background: Multifocal tuberculosis is defined as the involvement of at least two extra-pulmonary sites, with or without pulmonary involvement. The most commonly involved endocrine organ is the adrenal gland. We report a case of adrenal insufficiency revealing multifocal tuberculosis.Case report: A 65 year old female patient with no context of immunosuppression, presented to emergency department with Consciousness disturbance associated with severe hypon...

ea0099ep1164 | Adrenal and Cardiovascular Endocrinology | ECE2024

Adrenal fusion during renal transplantation: A challenging situation

Dassoufi Rania , Nyogushima Eleazar , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Adrenal-renal fusion is a rare entity wherein the capsule of the adrenal gland is fused to the kidney. Generally asymptomatic, it is only in pathological situations or in cases of adrenal or renal resection that this situation can cause problems. Adrenal transplantation has long been studied in rats solely to treat adrenal insufficiency, but no cases of accidental transplantation have been reported. Here, we report a case of adrenal-renal fusion making intraopera...

ea0099ep1168 | Adrenal and Cardiovascular Endocrinology | ECE2024

Testicular adrenal rests in a patient with congenital adrenal hyperplasia: a case report and literature review

Ouakrim Hind , Ettalibi Fatiha , Rafi Sana , El Mghari Ghizlane , El Mghari Nawal

Introduction: Congenital adrenal hyperplasia (CAH) is a group of rare inherited autosomal recessive disorders, CAH is caused by a mutation in the CYP21A2 gene that leads to a deficiency of 21-hydroxylase (CYP21), due to CYP21A2 gene mutations. Testicular adrenal rest tumors (T-ARTs) is a rare kind of benign tumor in the testis, which occurs mainly secondary to congenital adrenal hyperplasia (CAH). We report a rare case of bilateral TART in a patient with CAH whose diagnosis wa...

ea0099ep288 | Calcium and Bone | ECE2024

Hyperparathyroidism: secondary to myeloma or concomitant association

Ouakrim Hind , Hassan Neima , Rafi Sana , El Mghari Ghizlane , El Ansari Nawal

Introduction: Hyperparathyroidism is a pathological condition characterized by the excessive secretion of parathyroid hormone (PTH), resulting from the hyperactivity of one or more parathyroid glands. This condition can manifest as primary, secondary, or tertiary hyperparathyroidism. However, determining the primary or tertiary origin of hyperparathyroidism can pose challenges in certain complex situations. In this report, we present a clinical case where identifying the prima...