Searchable abstracts of presentations at key conferences in endocrinology

ea0073aep813 | Late Breaking | ECE2021

Three faces of the metabolic syndrome in children

Ioana Arhire Amalia

IntroductionAs the incidence of pediatric obesity is increasing, so is the incidence of metabolic syndrome in the pediatric population. We present the management of 3 such cases.Case reportThree 14 (D.D), 15 (C.A.), 16 (C.M) year-old males presented for weight and metabolic management.DD had a medical history weight gain since 2 years old, obesity, dyslipidemia, hyperuricemia. C.A., obese since 2018, with hyp...

ea0090ep1121 | Late Breaking | ECE2023

Vitamin D status in childhood obesity: prevalence and implications in a group of children from Romania

Ioana Arhire Amalia , Steluta Boroghina , Ancuta Ionita

Introduction: Obesity and vitamin D deficit are risk factors for inflammation, insulin resistance, hypertension and impeded bone mineralization and also cardiovascular disease. type 2 diabetes and osteoporosis. As globally both conditions reach pandemic levels and the level of vitamin D negatively correlates with obesity we studied this correlation and impact on a group of children suffering from obesity.Materials and method: We conducted a retrospective...

ea0063p785 | Thyroid 2 | ECE2019

Never too late for a papillary thyroid carcinoma recurrence

Ioana Arhire Amalia , Oprea Theodor , Stanciulescu Raducu , Gabriela Barbu Carmen

Introduction: We report a case of papillary thyroid carcinoma recurrence. According to most of the guidelines, patients with PTC have recurrences in the first 5 years after diagnosis and the most rigorous follow-up is indicated in this time; however metastasis are reported beyond this period and are associated mostly with lack of adherence to follow-up.Case report: A 76-year-old female was admitted in our department for the evaluation of a 5 cm laterocer...

ea0041ep118 | Bone & Osteoporosis | ECE2016

Incident fragility fractures under antiresorbtive therapy in a 76 year old lady: never too late to discover new causes

Ioana Arhire Amalia , Tudose Cornelia , Florea Suzana , Gabriela Barbu Carmen

Introduction: We report a case of severe osteoporosis with incident fragility fractures during antiresorbtive therapy in the presence of amiodarone induced hypothyroidism.Case report: A 76 year old female was admitted in our department for the evaluation of antiresorbtive therapy in the context of a recent rib fracture after coughing. Severe osteoporosis (lumbar T-score: −2.8DS, femoral neck T-score: −2.9DS with multiple fra...

ea0070ep489 | Thyroid | ECE2020

Thyroglobulin vs imaging in late recurrent metastatic thyroid carcinoma

Ioana Arhire Amalia , Gabriela Barbu Carmen , Theodor Oprea

Introduction: As the incidence of thyroid cancer is increasing, so are the cases of recurrence with RAI refractory metastasis of thyroid differentiated cancer. We present such a caseCase report: A 77-year-old female with a medical history of papillary thyroid carcinoma recurrence 10 years after surgery with successful 3 RAI sessions and normal thyroid cancer markers after treatment until her recurrence a year ago, with TSH unstimulated thyroglobulin of 1...

ea0049ep587 | Diabetes therapy | ECE2017

A rare pediatric presentation of type 1 diabetes mellitus with duchenne muscular dystrophy - what to expect in the future?

Elena-Iuliana Pascu-Gabara , Ioana Arhire Amalia , Sorin Ioacara , Simona Fica

Introduction: Duchenne muscular dystrophy (DMD) is a genetic condition caused by mutations in the X-linked dystrophin-gene leading to muscle degeneration and early death in males.Since DMD is characterized by aggressive inflammation it is recommended the use of pharmacological treatment with corticosteroids (CS). Type-1 diabetes mellitus (T1DM) is one of the most common chronic diseases in childhood and is caused by insulin deficiency resulting from the autoimmune destruction ...

ea0037ep1166 | Clinical Cases–Pituitary/Adrenal | ECE2015

A rare case of primary empty sella syndrome and growth hormone excess in a patient with neurofibromatosis type 1

Iuliana Pascu Elena , Mihaela Epure , Ioana Arhire Amalia , Sorina Martin , Simona Fica

Introduction: Neurofibromatosis type 1 (NF1) is the most common type of NF, and accounts for about 90% of all cases. Primary empty sella syndrome (ESS) results from herniation of arachnoid mater into the pituitary fossa. Since it has been demonstrated that the small anterior pituitary size reflects loss of neurofibromin expression in the hypothalamus, leading to reduced GHRH, pituitary GH and IGF1 production, we agree that IGF1 and GH increased in our patient can be challengin...

ea0070aep237 | Bone and Calcium | ECE2020

Is BMD still useful when we have FRAX?

Oprea Theodor-Eugen , Nistor Irina , Ioana Arhire Amalia , Alexandru Elena , Alice Albu , Sorina Martin Carmen , Sirbu Anca , Gabriela Barbu Carmen , Simona Fica

Introduction: The FRAX fracture risk assessment algorithm is able to integrate clinical risk factors independent of bone mineral density (BMD), evaluating the 10-years probability of fracture, therefore identifying patients in need for antiosteoporotic treatment, in which case bypassing the WHO (World Health Organization) criteria for densitometric diagnosis of osteoporosis.Material and Methods: We retrospectively analysed a total of 91 scans of women ag...