Searchable abstracts of presentations at key conferences in endocrinology

ea0065cc7 | FEATURED CLINICAL CASE POSTERS | SFEBES2019

Arg798Ter BRIP-1 mutation associated with metastatic phaeochromocytoma

Gohil Shailesh , Barwell Julian , Levy Miles

Case: A 69 year old gentleman with a past medical history of essential hypertension presented to medical services with symptoms of weight loss, muscle weakness and fatigue. Following blood tests, a CT scan, liver biopsy and biochemical screening, a metastatic phaeochromocytoma was diagnosed. He was commenced on alpha and beta blockade. Further imaging, including a MIBG scan, showed non-resectable disease therefore he underwent therapeutic MIBG treatment. Following a good respo...

ea0063p329 | Reproductive Endocrinology 1 | ECE2019

Randomised Controlled Trials in women with polycystic ovary syndrome do not represent the majority of patients who are in a primary care setting: systematic review and meta-analysis

Liarakos Alexandros Leonidas , Levy Miles , Mani Hamidreza

Introduction: Polycystic Ovary Syndrome (PCOS) is the most common endocrinopathy in women of reproductive age, with important long term health consequences such as higher chance of developing Type 2 diabetes, reduced overall wellbeing with poor quality of life. Such a common condition is mainly treated and investigated in the primary care setting.We therefore set out to see if the randomized controlled trials (RCT) represent the most common setting of care.<p class="abstex...

ea0044ep2 | (1) | SFEBES2016

Cushing’s disease detected following an adrenal incidentaloma

Gohil Shailesh , Kieffer Veronica , Levy Miles

Background: Adrenal incidentalomas are classified as adrenal lesions picked up on imaging performed due to reasons other than to look at the adrenals. With cross sectional imaging becoming more frequent, the frequency of adrenal lesions being detected and referred to endocrine services is increasing and dedicated adrenal incidentaloma clinics are being set up to screen these patients for potential pathology.Case: We present a 63 year old lady who underwe...

ea0059p066 | Clinical practice, governance &amp; case reports | SFEBES2018

Cranial Diabetes Insipidus – A survey of patient safety concerns in secondary care

Gohil Shailesh , Reddy Narendra , Levy Miles

Background: Knowledge of Cranial Diabetes Insipidus (CDI) is poor amongst healthcare professionals. Intra-nasal Desmopressin sprays are often mistaken for pulmonary inhalers, and Diabetes Insipidus mistaken for Diabetes Mellitus, leading to incorrect management and harm. Correct Desmopressin administration and fluid management is paramount in inpatients, especially in reduced conscious states.Aim: To explore Clinicians’ concerns regarding safety iss...

ea0038p428 | Steroids | SFEBES2015

Complications of CAH in pregnancy

Archer Natasha , Roy Chandrima , Levy Miles

Case: A 32 year old with known classical 21 hydroxylase deficiency was planning her first pregnancy. She had a history of clitoral reduction and vaginal reconstructive surgery as a baby. Pre-conception control on prednisone and fludrocortisone was good: 17(OH) progesterone 8.3 nmol/l, androstenedione 9.8 nmol/l (0.7–10.8), testosterone 3.0 nmol/l (0.2–3). EUA showed a small vaginal opening and she was given vaginal dilators. She conceived successfully and was counsel...

ea0036oc7.5 | Oral Communications 7 | BSPED2014

The relationship of vibration perception threshold with metabolic control and duration of disease in British children with type 1 diabetes

Kallampallil Jins , Goodwin Simon , Riddle Miles

Introduction: Type 1 diabetes affects a large number of children and adolescents, and its incidence is on the rise worldwide. The most devastating and important consequence of diabetes is its role in the development of long-term microvascular complications. This study aimed to study the role of the non-invasive vibration perception threshold (VPT) test in detecting subclinical peripheral neuropathy, and its correlation with metabolic control and duration of disease in British ...

ea0036P13 | (1) | BSPED2014

Development of a premature adrenarche management guideline

Kiff Sarah , Bath Louise , Miles Harriet

Introduction/aims: Adrenarche, the gradual increase in adrenal androgen secretion resulting in clinical features of pubic hair, axillary hair, body odour and acne, is independent from gonadotrophin-dependent central puberty. It is important that children presenting with these features are not unnecessarily investigated, whilst ensuring significant pathology is not overlooked.There is variation in practice in management of adrenarche. We identified curren...

ea0028p151 | Neoplasia, cancer and late effects | SFEBES2012

Biochemical screening of adrenal incidentalomas may lead to early detection of MEN2A

Hamblin Ross , Gleeson Helena , Levy Miles

A forty-three year old woman (SR) presented to her GP in 2004 with persistent back pain. Following MRI, an incidental right adrenal mass was discovered. Laparoscopic adrenalectomy was performed in the private sector and histology was consistent with a phaeochromocytoma. No further biochemical investigations were performed at that stage. Six years later, her fourteen year old daughter presented with a solitary neck lump. Fine needle aspiration was inconclusive and subsequent le...

ea0015p69 | Clinical practice/governance and case reports | SFEBES2008

A case of hypercalcaemia due to ectopic PTH secretion

Witherall Ruth , Levy Miles , Howlett Trevor

A 67-year-old lady with no significant past medical history presented with a left-sided neck swelling. An FNA under ultrasound scan guidance revealed malignant cells of indeterminate origin. Left neck exploration revealed an enlarged left lobe of thyroid and a retrosternal mass extending into the aortic arch. A left thyroid lobectomy and removal of retrosternal mass was performed and the histology showed a thyroid colloid goitre and low grade paraganglioma respectively. She wa...

ea0013p59 | Clinical practice/governance and case reports | SFEBES2007

How do we manage adrenal “incidentalomas” – an audit of referrals to a teaching hospital endocrine unit

Higgins Kath , Levy Miles , Howlett Trevor

We audited the management of adrenal incidentaloma (AI) in our hospital.29 patients (12 male) were referred with AI, mean age 68y (48–87 years). Mode of detection: 7 ultrasound (2 no mass on subsequent CT/MRI), 20 CT, 1 MRI and 1 lumbar XR. Site of tumour: 18 right, 7 left, 1 bilateral, 1 N/A. Size: <4 cm in 17, 4–6 cm in 4, >6 cm in 2, “large” in 1, not stated in 4. History: 8 had clinical features of possible hormone excess....