Searchable abstracts of presentations at key conferences in endocrinology

ea0056p44 | Adrenal cortex (to include Cushing's) | ECE2018

Adrenal insufficiency in treated PMR: The tip of the iceberg

Sagar Rebecca , Abbas Afroze

Background: Prolonged, high dose glucocorticoid therapy is used in to treat a number of rheumatological diseases, including polymyalgia rheumatica (PMR), giant-cell arteritis (GCA) and large vessel vasculitis (LVV). However there can be significant consequences of long-term glucocorticoid use, including iatrogenic adrenal insufficiency, due to suppression of the hypothalamic-pituitary-adrenal axis. This study aims to evaluate the prevalence, investigation and recovery of iatro...

ea0094p257 | Neuroendocrinology and Pituitary | SFEBES2023

A complex case of Acromegaly, resistant to treatment & discovered during pregnancy; A regional, collaborative approach

May Caroline , Kinton Rebecca

Background: Acromegaly is a rare Endocrine condition caused by excessive secretion of growth hormone; in 2022, there were approximately 3500 people with a known diagnosis in the UK. Patients with Acromegaly can achieve successful remission of the disease with medical therapy, pituitary surgery and radiotherapy (sometimes a single treatment, sometimes combination). However, these treatment options have associated risks, including side effects, late effects of r...

ea0027oc2.7 | Oral Communications 2 (Quick Fire) | BSPED2011

Selective reduction in trabecular bone mineral density during treatment for childhood acute lymphoblastic leukaemia

Sands Rebecca , Moon Rebecca , Doherty Lianne , Kohler Jan , Davies Justin

Introduction: Fracture incidence is increased during and after treatment for childhood acute lymphoblastic leukaemia (ALL). Studies using DXA, which measures a composite of both trabecular and cortical bone mineral density (BMD), have shown reduced BMD during treatment. We therefore used peripheral quantitative computed tomography (pQCT) to investigate changes in compartmental (cortical and trabecular) volumetric BMD (vBMD) and bone geometry, and evaluated the influence of tre...

ea0078OC7.5 | Oral Communications 7 | BSPED2021

Screening for eating disorders in young people with type 1 diabetes

Jacob Rebecca , Braha Nirit , Ladha Ruhina

Background: Eating disorders (ED) are more prevalent in young people with Type 1 diabetes than their peers and the combination is associated with higher levels of mortality. However, ED are often under-identified in paediatric diabetes services. Using quality improvement methodology, a screening pathway for ED was developed. Methods: Questionnaires and semi-structured interviews explored participants’ views regarding a screening pathway and choice o...

ea0053cd1.3 | Case Discussions: complex clinical cases 1.0 | OU2018

Early screening for gestational diabetes in obese pregnant women is associated with improved neonatal and maternal outcomes

Ryan David , Haddow Laura , Reynolds Rebecca

Gestational Diabetes (GDM) complicates 3–5% of all UK pregnancies but prevalence is increasing with rising rates of maternal obesity. Adaptions to the GDM screening protocol within NHS Lothian in August 2016 to screen high-risk women including women with obesity (BMI≥30 kg/m2) during early pregnancy (approximately 10 weeks gestation) allowed us to test the hypothesis that early screening of obese pregnant women would be associated with improved maternal a...

ea0051p015 | Gonadal, DSD and reproduction | BSPED2017

Consensus for UK principles of management of adolescents and infants with Disorders of Sex Development (DSD)

Matthews Rebecca , Crowne Elizabeth C , Skae Mars

Disorders of sex development (DSD) are a group of conditions caused by atypical development of chromosomal, gonadal or anatomical sex which pose complex, long-term diagnostic, investigative and management challenges requiring expert teams and close collaboration with families and peer groups. The lack of nationally agreed clinical standards for the management of DSD has been recognised by the British Society of Paediatric Endocrinology and Diabetes, and these are now in develo...

ea0085p59 | Diabetes 2 | BSPED2022

An Alternative Case of Diabetes

Alcorn Claire , Abid Noina , Heyburn Rebecca

AimsTo present a case of steroid induced diabetes and use this opportunity to review the diabetic resources we provide to other speciality teams in our hospital. CaseA fifteen year old patient was diagnosed with acute lymphoblastic leukaemia from a full blood count and bone marrow biopsy following a short history of lymph node swelling. He was started on a treatment regime that included dexamethasone at a dose of 6mg/m2</...

ea0086p19 | Adrenal and Cardiovascular | SFEBES2022

An Audit of Adrenal Vein Sampling in a large teaching hospital in Leeds

Lim Joyce , Sagar Rebecca , Abbas Afroze

Introduction: Primary hyperaldosteronism (PA) can affect up to 10% of patients with hypertension. Adrenal vein sampling (AVS) is used to distinguish between unilateral and bilateral aldosterone production. However, it is invasive, technically challenging and is only performed in a limited number of centres. This audit aimed to evaluate the effectiveness of AVS in informing the management of PA in a large teaching hospital.Methods: A retrospective audit o...

ea0068p34 | Abstracts | UKINETS2019

Neuroendocrine breast metastases: difficulties in interpretation of pathology and distinction from breast cancer

Kayani Mahaz , Anthoney Alan , Slater Rebecca Milican

Neuroendocrine tumours presenting in the bronchial or gastrointestinal tract often present with metastatic disease. Whereas well recognised sites of metastases include liver, lymph nodes and bones, they can also arise in unusual locations sometimes causing difficulties in diagnosis. The breast is an uncommon site for neuroendocrine tumour metastasis with estimates that it represents 0.1% of all breast tumours. Due to the low incidence of these neoplasms and due to difficulties...

ea0065p32 | Adrenal and Cardiovascular | SFEBES2019

An unusual case of adrenal cortical carcinoma presenting with hypogonadotrophic hypogonadism

Sagar Rebecca , Gibbons Stephen , Abbas Afroze

We report the case of a 52 year old gentleman who presented to Primary Care with a short history of gynaecomastia, loss of libido and erectile dysfunction. He was normally fit and well, with no past medical history and no regular medications. Initial blood tests showed low testosterone (0.7 nmol/l (normal 11–28)) with inappropriately low gonadotrophins (LH 1.2iU/l (1.5–9.3), FSH <0.1 iU/l (1.4–18.1)). Other blood tests were unremarkable (TFTs, prolactin, FBC...