Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep307 | Calcium and Vitamin D metabolism | ECE2015

Hypercalcaemia in patient with primary hyperparathyroidism and acromegaly

Pemovska Gordana , Ilijevska Cvetanka Volkanovska , Krstevska Brankica

Introduction: Hypercalcaemia in acromegaly can be a result of several pathophysiological mechanisms. Multiple endocrine neoplasia type 1 (MEN1) syndrome, mitogenic effect of hyperactivated GH–parathyroid gland axis, i.e. primary hyperparathyroidism and hypercalcaemia mediated by elevated 1,25-dihydroxyvitamin D should be considered.Case report: We describe a case of acromegaly associated with primary hyperparathyroidism. A 52-year-old female was dia...

ea0037ep980 | Thyroid (non-cancer) | ECE2015

Effect of L-thyroxine on left ventricular function in subclinical hypothyroidism

Nakova Valentina Velkoska , Krstevska Brankica , Kostovska Elizabeta Srbinovska , Pemovska Gordana

Introduction: Thyroid hormone deficiency can lead to the impairment of cardiac function. Whether subclinical hypothyroidism (ScH) is a risk factor for left ventricular (LV) dysfunction is controversial. Aim of the study was to assess whether ScH is associated with LV systolic and diastolic dysfunction and it’s reversibility after treatment with L-thyroxine.Material and methods: Twenty-seven consecutive patients with newly diagnosed Sc...

ea0032p955 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Atypical McCune–Albright syndrome associated with GH secreting pituitary adenoma

Pemovska Gordana , Volkanovska - Ilijevska Cvetanka , Krstevska Brankica , Ahmeti Irfan

McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD), cutaneous cafe-au-lait pigmentation and autonomous hyper-secretory endocrinopathies. Association of acromegaly with MAS is very rare. We present a case of a 35-year-old men with MAS, diagnosed with poly-ostotic fibrous dysplasia at the age of 12, no history of premature puberty, with GH secreting cystic macroadenoma 40×35×45 mm big and clinical picture of acromegaly, hypopituitarism and b...

ea0081p225 | Thyroid | ECE2022

Comparison in lipid parameters before and after L-thyroxine treatment in subclinical hypothyroidism according to the presence of thyroid peroxidase antibodies

Velkoska Nakova Valentina , Krstevska Brankica , Cheshlaroska Markushoska Katerina , Jovanovska Mishevska Sasha , Milenkovic Tatjana

Objective: Subclinical hypothyroidism (ScH) is a common condition and may be associated with dyslipidemia. We investigated the effect of levothyroxine therapy (L-T4) on lipid parameters in patients with a mild form of subclinical hypothyroidism according to the presence of thyroid peroxidase antibodies (anti-TPO antibodies). Material and methods: Fifty-seven patients with newly diagnosed ScH (TSH levels between upper reference value and 10 mIU/l with nor...

ea0041ep1083 | Thyroid (non-cancer) | ECE2016

The beneficial effect of L-thyroxine on lipid parameters in mild form of subclinical hypothyroidism

Nakova Valentina Velkoska , Krstevska Brankica , Pemovska Gordana , Milenkovikj Tatjana , Vaskova Olivija

Introduction: Overt hypothyroidism and severe subclinical hypothyroidism (ScH) are associated with dyslipidaemia, and its condition is reversible after thyroid replacement therapy. We investigated the effect of levothyroxine therapy on lipid parameters in patients with mild form of subclinical hypothyroidism (ScH).Material and methods: Fifty-seven patients with newly diagnosed ScH with TSH levels below 10 mU/l and 30 age and sex-matched healthy subjects ...

ea0035p248 | Clinical case reports Pituitary/Adrenal | ECE2014

A primary adrenal adenomatoid tumor in a young woman

Krstevska Brankica , Misevska Sasha Jovanovska , Ahmeti Irfan , Jovanovska Biljana , Bitoska Iskra , Bogoeva Biljana

Adenomatoid tumors are relatively uncommon neoplasms of mesothelial origin, usually occuring in the male and female genital tracts. Rare extragenital adenomatoid tumor has been identified in adrenal gland. The differential diagnosis includes metastatic carcinoma and adrenocortical carcinoma.We present a case of 30 years old woman with incidentally radiological (ultrasound) finding of unilateral tumor in the right adrenal gland. CT and MRI were of great v...

ea0070aep92 | Adrenal and Cardiovascular Endocrinology | ECE2020

Cystic pheochromocytoma, a diagnostic challenge: A case report

Volkanovska Ilijevska Cvetanka , Hasan Taner , Malinovska-Nikolovska Liljana , Krstevska Brankica , Volkanovska Nikolovska Ance

We describe a case of cystic pheochromocytoma (PCC) with negative biochemical evaluation, diagnosed on the basis of hypertensive crises during operative management and histopathologic findings. A 57-year-old woman complained of several episodes of stabbing right upper abdominal pain accompanied by tachycardia, headache, lack of breath, elevated blood pressure and vomiting in the preceding three years. At presentation, blood investigations were significant only for mildly eleva...

ea0070ep518 | Thyroid | ECE2020

Management of subclinical hyperthyroidism presented by several cases

Velkoska Nakova Valentina , Krstevska Brankica , Pemovska Gordana , Ahmeti Irfan , Milenkovic Tatjana

Subclinical hyperthyroidism (ScHyper) is a condition with suppressed TSH, and normal free T3 and free T4 hormones, affecting 10% of the population. There are two subgroups of patients, the first group with TSH lower than 0.1 U/l, and the second group with mildly suppressed TSH between 0.1 and the lower assay reference limit. The patients from the first group should be treated, but there is no evidence for therapy for the second group of patients.We prese...