Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep487 | Thyroid | ECE2020

The association between thyroid anaplastic carcinoma and papilar carcinoma folicular version – longer life expectancy?

Nechita Mirela-Claudia , Tudurean-Olteanu Anca-Georgiana , Dumitru Teodora , Florescu Alexandru , Christina Ungureanu Maria

Introduction: Anaplastic thyroid carcinoma are highly aggressive solid tumors, with a median survival of less than 6 months after diagnosis. They typically occur in patients who are 65 years of age or older. On the other hand, papillary thyroid carcinoma and follicular thyroid carcinoma are generally indolent, with very few progressive cases.Case report: A 64-year-old patient with no significant pathological history, known with goiter for about 40 years ...

ea0070ep490 | Thyroid | ECE2020

Solitary fibrous tumour of the thyroid, features of a very rare tumour: A case report

Dumitru Teodora , Hrisa Anamaria , Nechita Mirela-Claudia , Ciobanu Delia , Danila Radu , Ungureanu Maria-Christina

Introduction: Solitary fibrous tumor (SFT) is a sporadic tumor, commonly found in the pleural cavity. It is like a large well-circumscribed mass, arising from mesenchymal tissue, with spindle cells proliferation, arranged in various patterns. SFT of the thyroid is exceptionally rare, with only about 28 cases being reported in the international literaterature.A 34-year-old woman presented in the Department of Endocrinology with the diagnosis of a multinod...

ea0063p490 | Calcium and Bone 2 | ECE2019

Hyperparathyroidism – jaw tumor syndrome – differential diagnostic traps

Nechita Mirela Claudia , Tudurean-Olteanu Anca Georgiana , Costan Victor Vlad , Danila Radu , Preda Cristina , Ungureanu Maria Christina

Introduction: Hyperparathyroidism-Jaw Tumor (HPT-JT) syndrome is a rare genetic disorder bearing a germline and a somatic CDC73 mutation. The features of HPT-JT are clinically difficult to ascertain because the parathyroid disease, ossifying fibroma in the jaw and other abnormalities, often occurs asynchronously and may be diagnosed and treated separately. The association of jaw ossifying fibroma with primary hyperparathyroidism (PHPT) is typical of HPT-JT.<p class="abstex...

ea0056p149 | Neuroendocrinology | ECE2018

Diagnostic difficulties, management and treatment in neuroendocrine tumors

Nechita Mirela Claudia , Tudurean-Olteanu Anca Georgiana , Hrisca Anamaria , Stefanescu Cipriana , Stolniceanu Cati Raluca , Florescu Alexandru , Ungureanu Maria Christina

Introduction: Diagnosis of NETs (neuroendocrine tumors) is based on clinical manifestations, peptide and amine secretion, specialized radiological and nuclear imaging, secured by detailed histology and immunohistochemistry, which should be obtained whenever possible. Biomarkers are still the mainstay in the diagnosis and follow-up of patients with NETs.Case report: We present the case of a 36-year-old patient with no significant pathological personal his...

ea0056p708 | Clinical case reports - Pituitary/Adrenal | ECE2018

Bromocriptine for management of a patient with cranipharyngioma and central hyperthermia after neurosurgery: a case report

Tudurean-Olteanu Anca-Georgiana , Hrisca Anamaria , Nechita Mirela Claudia , Rotariu Daniel , Preda Cristina , Leustean Letitia , Ungureanu Maria Christina

Introduction: Central hyperthermia is frequent in patients with brain injury and is characterized by a rapid onset with high temperatures, marked temperature fluctuations and poor response to antipyretics. It is associated with worse outcomes in the injured brain, thus it is important to aggressively manage it.Case-report: We report a case of a 9-year-old boy diagnosed with sellar and suprasellar adamantimomatous craniopharyngioma at the age of 5 when he...

ea0056p96 | Clinical case reports - Pituitary/Adrenal | ECE2018

From gastric sleeve to diagnosis of a rare familial multiple endocrine neoplasia type 1

Tudurean-Olteanu Anca Georgiana , Danila Radu , Nechita Mirela Claudia , Dumitrascu Andreea-Nicoleta , Preda Cristina , Leustean Letitia , Hrisca Anamaria , Ungureanu Maria Christina

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal-dominant hereditary disorder characterized by the presence of two of the three main endocrine tumors that are parathyroid, pituitary adenomas and enteropancreatic tumors.Case-report: We report a case of a 71-year-old obese patient with repeated unsuccessful attempts to weight loss who was admitted to the surgical department for the bariatric treatment of obesity (BMI=48,22 kg/m...