Searchable abstracts of presentations at key conferences in endocrinology

ea0044ep113 | (1) | SFEBES2016

A big price for a little mistake: similar presentations but diverse management of thyroid storm

Iftikhar Mawara , Crown Anna

Introduction: Thyroid storm is a rare endocrine emergency associated with the reported mortality rate ranging from 10 to 20%. We discussed the management of two cases of thyroid storm with different outcomes. It also showed the successful use of ECMO in the management of severe hyperthyroidism related cardiomyopathy and circulatory collapse.Case History 1: A 36 years old female with known history of Graves’ disease, presented with palpitations and s...

ea0037ep156 | Reproduction, endocrine disruptors and signalling | ECE2015

An audit of prevalence and management of erectile dysfunction and LUTS in a diabetes clinic?

Haley Anna , De Parijat

Introduction: UK NICE guidelines recommend that men with diabetes mellitus (DM) should be reviewed annually regarding symptoms of erectile dysfunction (ED) in view of possible phosphodiesterase-5 (PDE-5) inhibitor treatment. Previous studies have shown that 70% of men with ED have concomitant lower urinary tract symptoms (LUTS). It has been suggested that there may be some common patho-physiology accounting for the improvement in LUTS seen in men with ED and LUTS treated with ...

ea0037ep320 | Diabetes (pathiophysiology & epitemiology) | ECE2015

Changing of expression of NOD-like receptors in GALT of rats at an experimental diabetes mellitus and pentoxifylline administration

Kamyshny Alex , Degen Anna

Introduction: Changing of expression of pattern-recognition receptors (PRR) of innate immune response by the gut-associated lymphoid tissue (GALT) can play a critical role in an induction and progression of T1DM.Aim: To study the peculiarities of NOD2 receptors in gut-associated lymphoid tissues (GALT) of rats with experimental STZ-induced diabetes mellitus and pentoxifylline (PTX) administration.Methods: Researches were made on Wi...

ea0037ep335 | Diabetes (pathiophysiology & epitemiology) | ECE2015

Relationship between adiponectin and anthropometric parameters, insulin resistance and transaminase levels in patients with nonalcoholic fatty liver disease and type 2 diabetes

Zhuravlyova Larysa , Zhuravlyova Anna

The basis of the pathogenesis of nonalcoholic fatty liver disease (NAFLD) is insulin resistance (IR) which appears on the background of abdominal obesity (AO) which, in turn, is a key factor in the emergence of an imbalance between adipocytokines entailing a disturbance of lipid and carbohydrate metabolism, which ultimately leads to the damage of the liver cells, the development of inflammation, fibrosis and apoptosis. The goal – to study features of changes in the level ...

ea0037ep444 | Diabetes (complications & therapy) | ECE2015

Prevalence and management of peripheral diabetic neuropathic pain in a hospital diabetes clinic: how are we doing?

Haley Anna , De Parijat

Introduction: Peripheral diabetic neuropathic pain (PDNP) as a significant complication of diabetes mellitus (DM), which is present in 16–26% of patients. NICE UK guidelines recommend that physicians should make an formal enquiry about distressing neuropathic symptoms annually and that either duloxetine, amitriptyline, gabapentin, or pregabalin should be used as first-line treatment for neuropathic pain.Aims: To assess the prevalence PDNP in a diabe...

ea0037ep828 | Pituitary: clinical | ECE2015

A case of adrenal crisis secondary to ipilimumab-induced autoimmune hypophysitis

Todd Anna , Thiraviaraj Athinyaa

A 42-year-old man undergoing ipilimumab therapy for stage IV metastatic melanoma presented after his third dose with vomiting, abdominal pain, hypotension, and pyrexia. He was treated as a presumed line sepsis. Four days prior to admission, thyroid function test showed T4 of 7.9 pmol/l and TSH 0.02 mU/l and he was treated with levothyroxine. A pituitary profile was carried out on admission and the results were as follows, cortisol was 24 nmol/l, testosterone <0....

ea0036P54 | (1) | BSPED2014

Transient hyperphosphatemia and hyperparathyroidism in a preterm neonate

Power Anna-Louise

Introduction: I report the case of a premature neonate who developed a transient hyperphosphatemia at 1 month of age with associated hyperuremia, hypercreatininemia and hyperparathyroidism.Case report: This baby girl was born by emergency caesarean section for maternal APH at 27+6 weeks. She had an uneventful neonatal period with minimal ventilation. She was treated with ibuprofen, amilorone and frusemide for a PDA with associated heart failure. Her ente...

ea0035p787 | Obesity | ECE2014

The association between metabolic syndrome and android fat mass and android to gynoid fat mass ratio- are Classification and Regression Trees models helpful?

Brona Anna , Milewicz Andrzej

The aim of the study was to estimate thresholds of android fat mass and android to gynoid fat mass ratio at which metabolic disorders and blood pressure typical of metabolic syndrome appear. Classification and Regression Trees models were used to estimate these thresholds for glucose, HDL cholesterol, triglycerides and systolic and diastolic blood pressure.Methods: healthy postmenopausal women were recruited for the study. Blood samples were collected fo...

ea0070aep935 | Thyroid | ECE2020

Thyroglossal duct cyst papillary thyroid cancer in a 40-year-old female: Case report

Dabrowska Anna , Dudka Jaroslaw

Introduction: The thyroglossal duct develops during thyroid gland formation and usually involutes at 7–10 weeks gestation. Its residue can lead to formation of cysts as well as to develop neoplasms within the mass.Case report: A 40-year-old woman was admitted to Department of Otolaryngology because of an enlarging midline neck mass for the last few months, without other worrisome symptoms. A neck ultrasound and CT scan showed a cystic lesion with s...

ea0032p238 | Clinical case reports – Pituitary/Adrenal | ECE2013

Craniofacial fibrous dysplasia and pituitary gigantism in a 10-year-old boy: clinical case

Gusova Anna , Mazerkina Nadezhda

Introduction: The combination of poly/monostotis fibrous dysplasia, café-au-lait pigmentation of the skin and endocrine hyperfunction (mostly precocious puberty) is known as McCune–Albright syndrome (MAS), a genetic origin syndrome with low incidence. The molecular basis of MAS is a mosaic activating mutation of the α subunit of the G protein (Gsα) gene.We present a clinical case of a 10-year-old boy with partial MAS and GH-secreting ...