Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep940 | Reproductive and Developmental Endocrinology | ECE2023

Testicular Regression Syndrome: A Case Report

Amira Ikram , Azriouil Manal , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Testicular regression syndrome is defined as partial or complete absence of testicular tissue in the presence of a normal 46,XY male karyotype. This syndrome is very rare with an estimated prevalence of 1 case/20.000 males. Here we decribe a case of a testicular regression syndrome in an 18 years old patient. Case Report : We report the case of an 18 years old male patient followed for testicular regression syndrome since the age of 2, whic...

ea0081ep850 | Pituitary and Neuroendocrinology | ECE2022

Polyuro-polydipsia syndrome revealing a craniopharyngioma in a 60-year-old female patient following a surgery

Mhamdi Zineb , Amira Ikram , Rifai Kaoutar , Iraqi Hinde , El Hassan Gharbi Mohamed

Introduction: Craniopharyngioma is a benign, slow-growing epithelial tumor of embryonic origin, originating in the pituitary stem or pituitary gland and developing in the sellar and/or suprasellar region. It is characterized by its considerable potential for extension, its tendency to recur, and its adhesions to surrounding structures.Case report: We report the case of a 60-year-old female patient with secondary amenorrhea at the age of 38 years, neglect...

ea0081ep991 | Thyroid | ECE2022

Thyroid abscess as a complication of post-COVID-19 subacute thyroiditis: a case report

Guissi Loubna , Amira Ikram , Rifai Kaoutar , Iraqi Hind , Gharbi Mohamed Elhassan

Introduction: Thyroid abscess is a rare pathology, with the incidence of less than 1% of all thyroid diseases. We describe a unique case of thyroid abscess complicating post-covid-19 thyroiditis, which is the first case reported in Morocco to our knowledge.Case presentation: A 39-year-old man who had recently recovered from a mild episode of COVID-19 infection, consulted for weight loss, palpitations and neck pain. Examination of the neck revealed enlarg...

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...

ea0090ep757 | Pituitary and Neuroendocrinology | ECE2023

A dwarfism revealing a Pituitary stalk interruption syndrome (PSIS) at the age of 36 years

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

Introduction: Pituitary stalk interruption syndrome (PSIS) is a distinct developmental defect characterized by a thin or absent pituitary stalk, hypoplasia of the adenohypophysis, and ectopic location of the neurohypophysis.Case report: A 36 years old male patient, full term born by vaginal delivery, with birth asphyxia. Birth weight was 2800 g, length was 51 cm, and no other postnatal events were noticed. Psychomotor milestones were achieved normally. h...

ea0090ep939 | Reproductive and Developmental Endocrinology | ECE2023

An Intellectual Development Disorder Revealing A Rare Variant of the Klinefelter Syndrome – 48, XXXY: A Case Report

Amira Ikram , Guissi Loubna , Azriouil Manal , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Klinefelter syndrome is a sex chromosomal aneuploidy caused by an addition of X chromosome in males (47,XXY). 48,XXXY is a rare variant of this syndrome which is characterised by the presence of two additional X chromosomes in males and is estimated to occur in 1/50 000 male births. Here we describe a rare case of a 48, XXXY Klinefelter’s variant in a 17 years old patient revealed by an intellectuel development delay. Case Report : The...

ea0090ep1037 | Thyroid | ECE2023

Coexistence of thyroid carcinoma and graves’ disease: report of two cases

Azriouil Manal , Qasdi Ikrame , Amira Ikram , Rifai Kaoutar , Hinde Iraqi , Gharbi Mohamedelhassan

Introduction: Graves’ disease (GD) is a common autoimmune thyroid disease. The association between GD and thyroid carcinoma (TC) remains controversial. We describe two patients presenting this association.Case report: Case 1 a 46 years old woman with clinical history of type 2 diabetes, she was diagnosed with Graves’ disease and multiple nodules were found in her enlarged thyroid gland by ultrasonography. The patient underwent total thyroidecto...