Searchable abstracts of presentations at key conferences in endocrinology

ea0012p128 | Thyroid | SFE2006

Pulverised thyroxine could be the answer

Elmalti Akrem , Hammond Peter

A 36 year old lady referred to the endocrinology clinic, with a history of tiredness, fatigability and abnormal thyroid function. She had no significant past medial history, no family history of thyroid disease and her only medication was an oral contraceptive pill (Ovranette). She had experienced fatigue over a period of 5 years, since returning from a visit to Pakistan, during which she had developed diarrhoea which had persisted for about 12 months. Thyroid function tests a...

ea0074ncc42 | Highlighted Cases | SFENCC2021

Lithium-induced polyendocrinopathy in a single patient

Shah Preet , Hammond Peter

Case history: A 50-year-old lady, on Lithium for 30 years, presented with a history of progressively increasing thirst since 12 months; associated with polyuria and nocturia. She had been having some joint aches and was finding it more difficult to get up and down stairs. She was found to be hypothyroid few months back and prior to that had been falling asleep easily. There had been an improvement in her energy levels after starting Levothyroxine. She gave no history of renal ...

ea0074ncc52 | Highlighted Cases | SFENCC2021

Unmasking of hyperthyroidism by Takotsubo cardiomyopathy

Shah Preet , Hammond Peter

Case History: A 74-year-lady with a background of COPD presented to the emergency department with precordial chest pain radiating to the left arm. The pain had been ongoing since a few hours, and was associated with diaphoresis. She was hemodynamically stable, with no tachycardia Investigations: ECG showed significant ST-segment elevations, predominantly in the chest leads, with elevated troponins. Assuming it to be STEMI, she was transferred to the tert...

ea0032p963 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Pasireotide in treatment of Cushing’s disease: our first experience

Vanuga Peter , Kentos Peter , Pavai Dusan , Pura Mikulas

Background: Although the excision of ACTH-producing tumors is the principal treatment for Cushing’s disease (CD), pharmacologic treatment has a well-established role. As corticotroph adenomas express somatostatin (SST) receptors (SSTRs), pasireotide – a pluripotent somatostatin analogue, acting on four of five SSTRs has a potential role in treatment of CD among various medical agents.Case report: We report a 39-year-old female with recurrence o...

ea0026p546 | Bone/calcium/Vitamin D | ECE2011

Conservative therapy by cinacalcet for primary hyperparathyroidism management: first results of two center prospective study

Kentos Peter , Banarova Adriana , Pura Mikulas , Vanuga Peter , Payer Juraj

Introduction: Parathyroid hormone (PTH) secretion is regulated by the concentration of extracellular ionized calcium. The calcium sensing receptors (CaSR) of parathyroid chief cells play a central role in calcium homeostasis. Their activity is reduced by calcimimetics, the compounds that directly increase the sensitivity of CaSR to extracellular ionized calcium. Cinacalcet hydrochloride, an oral calcimimetic, is indicated in treatment of primary hyperparathyroidism (PHP), for ...

ea0022p66 | Adrenal | ECE2010

The HLA-DRB1 shared epitope and trans-encoded HLA-DQ-heterodimers hypothesis in autoimmune Addison disease

Pura Mikulas , Kuba Daniel , Kentos Peter , Chrenova Silvia , Vanuga Peter

Background: The MHC is the most important susceptibility locus for human autoimmune diseases (AID). Although associations between MHC class II DRB1 alleles and Addison disease (AD) have been repeteadly proven in various populations, the biological mechanisms underlying this association remains unknown. Peptide presentation to T cells may be important in the initiation or progression of AID. Disease-linked polymorphisms map to the peptide-binding sites of MHC molecules class II...

ea0099ep924 | Pituitary and Neuroendocrinology | ECE2024

Experiences with pasireotide treatment in subjects with acromegaly

Kužma Martin , Vanuga Peter , Jackuliak Peter , Payer Juraj

Currently, acromegaly is treatable by 3 groups of drugs available for the treatment of acromegaly: dopamine agonists (DA), somatostatin analogues (SRL) and a growth hormone receptor blocker (GH receptor antagonist GHRA). More recently, pasireotide and pasireotide-LAR were developed as multi-receptor targeted SRLs with higher potency than 1st generation SRLs/octreotide-LAR and lanreotide/and until now were considered second generation SRLs. Pasireotide, unlike first-generation ...

ea0065p408 | Thyroid | SFEBES2019

Weight trajectory during treatment for hyperthyroidism

Dicasillati Gaia Alhena , Taylor Peter

Objectives: Hyperthyroidism is associated with a high basal metabolic rate and weight loss is a common symptom. However, it has been observed, that once patients are treated, they gain back the lost weight and may also put on more. Given that weight gain is a health factor, there’s interest in studying the effect that the thyroid levels have on weight gain and potential harmful health consequences.Methods: 79 patients (58 female) with hyperthyroidis...

ea0016p100 | Bone and calcium | ECE2008

Agressive course of primary hyperparathyroidism caused by parathyroid carcinoma: case report

Vanuga Peter , Kentos Peter , Gres Alojz , Kalis Andrej , Povinec Peter , Pura Mikulas

Parathyroid carcinoma (PTCa) is an uncommon cause of primary hyperparathyroidism (PHP), statistically representing <1–2% of all cases of PHP. Early resection of the primary tumor is the only curative treatment, however this is frequently incomplete. As a consequence, recurrence of PTCa presenting as locally invasive tumor and/or metastatic process is not rare. Morbidity and mortality are generally caused by the effects of unremitting hypercalcemia rather than tumor gr...

ea0055p21 | Poster Presentations | SFEEU2018

A catastrophic case of adrenal insufficiency

van Heeswijk Isabelle , Robinson Robert , Toth Peter

Case history: A 50 year old female presented with diarrhoea, facial rash and hyponatraemia. In addition, she described a 3 week history of headaches, malaise, intermittent joint pain and swelling. On examination, the patient was noted to have a malar rash and over the subsequent 2–3 days began to develop necrotic patches on both ears. She had no evidence of cutaneous pigmentation. She took no regular medication, other than dabigatran. Past medical history of note included...