Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep240 | Bone & Osteoporosis | ECE2017

Trabecular bone score is negatively associated with bone resorbtion markers in patients with primary hyperparathyroidism

Grigorie Daniel , Ivan Mirela , Caragheorgheopol Andra , Paun Diana , Sucaliuc Alina

Objectives: Mean TBS (Trabecular Bone Score) values are generally lower in PHPT (primary hyperparathyroidism) patients than controls. The aim of this study was to assess TBS from spine DXA images in patients with PHPT and look at its correlates.Methods: This was a cross-sectional study conducted in an osteoporosis referral center. One hundred and thirty six patients with PHPT were selected from our database (2010–2016) if they had a valid LS DXA sca...

ea0070ep526 | Thyroid | ECE2020

Central hypothyroidism secondary to oxcarbazepine therapy in children-a clinical case report

Mirica Alexandra , Mirica Radu , Monica Preda Diana , Loreta Paun Diana

Introduction: The change in thyroid parameters is described in the case of antiepileptic treatment in the pediatric population, due to interferences within the hypothalamo-pituitary-thyroid axis and due to the increase in the rate of hepatic metabolism of thyroid hormones.Case presentation: We present the case of a 10-year-old boy who addressed our outpatient pediatric endocrinology department for endocrine evaluation in the context of weight growth abou...

ea0026p110 | Female reproduction | ECE2011

MTHFR mutations in female patients with autoimmune thyroiditis

Bulgar Alexandra , Brehar Andreea , Paun Diana , Dumitrache Constantin

Introduction: Methylenetetrahydrofolate reductase (MTHFR) is a key regulatory enzyme involved in folate and homocysteine metabolism. The enzyme is encoded by a gene located on chromosome 1p36.3. MTHFR mutations frequently met in the population are C667T and A1298C. The impairment of homocysteine metabolism due to MTHFR gene polymorphism influences the risk for diseases such as CVS diseases, certain types of cancer and is associated with certain complications of pregnancy inclu...

ea0016p325 | Endocrine tumours | ECE2008

Mutations in the ret proto-oncogene in Romanian patients with multiple endocrine neoplasia type 2

Paun Diana , Duta Carmen , Mohora Maria , Dogaru Cristian , Dumitrache Constantin

Multiple endocrine neoplasia (MEN) is characterized by the occurrence of tumors involving two or more endocrine glands; MEN 2 is defined by medullary thyroid carcinoma in association with phaeochromocytoma and appears in several clinical variants, which may be inherited as autosomal dominant syndromes. Mutational analysis of RET protooncogene has been use in the diagnosis and management of patients and families with MEN 2 variants.Aim: In this study, we ...

ea0014p442 | (1) | ECE2007

Neuropsychiatric manifestations in patients of primary hyperparathyroidism and outcome following surgery

Raceala Alexandra , Ivanov Paul , Octavian Vasiliu , Paun Diana

Background: Primary hyperparathyroidism (PHPT) associates many psychiatric symptoms and is therefore important to find out if surgery can alleviates the psychiatric symptoms and improve the quality of patient’s life.Objectives: To study the nature and severity of neuropsychiatric manifestations in patients diagnosed with hyperparathyroidism before and after surgery, as well as to evaluate the correlation of such symptoms with levels of serum calcium...

ea0014p522 | (1) | ECE2007

L-thyroid hormone enhancement of antidepressant treatment in major depressive episode

Ivanov Paul , Raceala Alexandra , Vasiliu Octavian , Paun Diana

Objective: To determine the impact of combined antidepressant drugs and LT4 enhancers in treatment of patients with Major Depressive Disorder.Method: We conducted a randomized, placebo-controlled trial to determine whether LT4 supplementation had any augmentation effect on selective serotonin reuptake inhibitors (SSRIs). The study involved 70 patients with major depressive disorder; patients with hypothyroidism were excluded. Of the participants, 38 were...

ea0073ep143 | Pituitary and Neuroendocrinology | ECE2021

Pituitary stalk interruption syndrome: a clinical case report

Mirica Alexandra , Luiza Vitan , Monica Preda Diana , Loreta Paun Diana

IntroductionPituitary stalk interruption syndrome (PSIS) is a rare entity characterized by a triad of thin or interrupted pituitary stalk, aplasia or hypoplasia of the anterior pituitary and absent or ectopic posterior pituitary seen on magnetic resonance imaging (MRI). We are presenting the clinical case of a child who presented for short stature.Case presentationWe present the case of a 4 year and 8 months ...

ea0049ep122 | Clinical case reports - Pituitary/Adrenal | ECE2017

A rare case of a patient with MEN 4 phenotype and associated pheochromocytoma

Mirica Alexandra , Petris Rodica , Mirica Radu , Paun Sorin , Paun Diana Loreta

Introduction: MEN4 syndrome is a recently described form of MEN in patients with parathyroid and anterior pituitary tumors, which may also develop bronchial, gastric and pancreatic neuroendocrine tumors. In general, the patients present with clinical signs of primary hyperparathyroidism and simptoms caused by pituitary hormones hypersecretion or due to the tumor mass. However, clinical cases with the coexistence of pituitary tumors and pheochromocytoma are very rare described....

ea0041ep1163 | Thyroid cancer | ECE2016

Biphasic synovial sarcoma: an exceptional rare cervical mass

Ghemigian Adina , Carsote Mara , Petris Rodica , Dumitrascu Anda , Valea Ana , Terzea Dana , Paun Diana Loreta

Introduction: Synovial sarcoma represents a type of cancer derived from soft tissues; young males are more affected.Material and methods: This is a case report of a male with a cervical mass confirmed as sarcoma. Later on the investigations lead to the discovery of a thyroid nodule challenging the differential diagnosis. We assessed thyroid ultrasound, computed tomography (CT) at the cervical, thorax, mediastinum and abdomen; TSH (Thyroid Stimulating Hor...

ea0037ep1109 | Endocrine tumours | ECE2015

Papillary thyroid carcinoma in a patient with MEN 1 syndrome

Dumitru Alina , Paun Diana , Dragomir Adina , Nistor Mihaela , Taujan Georgiana , Dumitrache Constantin

Introduction: MEN1 is a rare syndrome characterised by hyperplasia or neoplasm of the parathyroid glands, pituitary, pancreas or duodenum and can associate, less frequently, phaeochromocytoma, thymic or bronchial carcinoids, multiple lipomas, cutaneous angiofibromas and thyroid adenomas.Case report: A 47-year-old woman with MEN1 presenting parathyroid recurrent adenomas, a pituitary prolactin-growth hormone cosecreting macroadenoma, associated with an in...