Searchable abstracts of presentations at key conferences in endocrinology

ea0050p298 | Neuroendocrinology and Pituitary | SFEBES2017

Diagnostic challenges in Cyclical Cushing’s syndrome presenting with Bilateral Central Serous Retinopathy

Freudenthal Bernard , Bouloux Pierre-Marc , Dorward Neil , Khoo Bernard , Cohen Mark

Case summary: A 55 year-old lady was referred by ophthalmology following diagnosis of bilateral central serous retinopathy, an accumulation of sub-retinal fluid at the fundus associated with Cushing’s syndrome. She also had proximal myopathy, bruising, centripetal weight gain and hypertension. Cushing’s was confirmed by 1 mg overnight DST (cortisol 581 nmol/L) and 48 hr-LDDST (407 nmol/L). 24 hr UFC was raised at 2666 nmol/L (12...

ea0050p298 | Neuroendocrinology and Pituitary | SFEBES2017

Diagnostic challenges in Cyclical Cushing’s syndrome presenting with Bilateral Central Serous Retinopathy

Freudenthal Bernard , Bouloux Pierre-Marc , Dorward Neil , Khoo Bernard , Cohen Mark

Case summary: A 55 year-old lady was referred by ophthalmology following diagnosis of bilateral central serous retinopathy, an accumulation of sub-retinal fluid at the fundus associated with Cushing’s syndrome. She also had proximal myopathy, bruising, centripetal weight gain and hypertension. Cushing’s was confirmed by 1 mg overnight DST (cortisol 581 nmol/L) and 48 hr-LDDST (407 nmol/L). 24 hr UFC was raised at 2666 nmol/L (12...

ea0082wd10 | Workshop D: Disorders of the adrenal gland | SFEEU2022

Cushing”s crises arising from a neuroendocrine tumour treated with etomidate infusion

Islam Quazi , Eltayeb Randa , Eldigair Hiba , Khoo Bernard , Yousseif Ahmed , Karra Efthimia , Patel Dipesh

Introduction: Ectopic ACTH syndrome is rare but is frequently severe condition because of the intensity of the hypercortisolism that may be dissociated from the tumoral condition. It should often be considered as an endocrine emergency requiring an emergency response both in terms of diagnostic procedures and therapeutic interventions. Patient management is complex and necessitates dual skills, in the diagnosis and treatment (1). Etomidate, an imidazole-derivative anesthetic a...

ea0037ep732 | Pituitary: clinical | ECE2015

Efficacy and safety of tolvaptan in treatment of SIADH; case-series from 2 UK hospitals

Tzoulis Ploutarchos , Waung Julian , Khoo Bernard , Cohen Mark , Bouloux Pierre-Marc

Introduction: Contrary to US guidelines, recent European guidelines do not recommend tolvaptan for the treatment of SIADH.Methods: Retrospective data collection of all inpatients treated with tolvaptan for SIADH in two UK hospitals between November 2010 and February 2014. All values were calculated as mean±S.D.Results: This case series included 61 patients (33 females, 28 males) aged 74.4±15.3 years with se...

ea0037ep745 | Pituitary: clinical | ECE2015

A 5 years retrospective studies looking at trends in water deprivation tests and roles for endocrine specialist nurses

Yeoh Phillip , Bouloux Pierre , Chew Shern , Khoo Bernard , Carroll Paul , Grossman Ashley

Performing water deprivation test (WDT) and prolonged water deprivation test (PWDT) is some of the roles undertaken by endocrine nurse in specialist endocrine units. These tests need to be done in a safe and control environment.Objectives: To provide safe information to patients to avoid fluids overload when they arrive for the tests. Can the specialist endocrine nurse make clinical decision to terminate the test base on clinical evidence and at what poi...

ea0031p111 | Clinical practice/governance and case reports | SFEBES2013

Adrenal incidentalomas: who requires further testing?

Paterson Fiona , Theodoraki Aikaterini , Amajuoyi Adaugo , MacLachlan Jody , Bouloux Pierre , Khoo Bernard

Adrenal incidentalomas are common and guidelines recommend testing to exclude functioning lesions and malignancy. Their increasing prevalence results in a number of investigations usually conducted in the Endocrinology clinic.In 2011 we audited the prevalence and management of adrenal incidentalomas identified on abdominal CT imaging over one calendar month in our centre. Consequently, a decision pathway for new adrenal lesions was introduced in the Radi...

ea0028p56 | Clinical practice/governance and case reports | SFEBES2012

Secondary adrenal suppression and Cushing’s syndrome caused by ritonavir boosted effects of inhaled fluticasone, injected triamcinolone and topical clobetasol: A case series of 11 patients.

Gurazada Kalyan , Marshall Neal , Johnson Margaret , Hillman Tobias , Bouloux Pierre , Khoo Bernard

The HIV protease inhibitor (PI) ritonavir is used in conjunction with other antiretroviral treatments as a pharmacokinetic booster due to its potent inhibition of hepatic cytochrome P450 3A4 (CYP3A4). Co-administration of glucocorticoids metabolized by CYP3A4, with ritonavir leads to accumulation of these glucocorticoids, markedly increasing the risk of iatrogenic Cushing’s syndrome and suppression of the Hypothalamic-Pituitary-Adrenal axis. We present 11 patients receivi...

ea0028p67 | Clinical practice/governance and case reports | SFEBES2012

Adrenal incidentalomas outside the Endocrinology clinic

Amajuoyi Adaugo , Theodoraki Aikaterini , MacLachlan Jody , Bouloux Pierre-Marc , Khoo Bernard

Adrenal masses discovered incidentally during imaging (adrenal incidentalomas) are common and constitute a common reason for referral in the Endocrinology clinic. Our aim was to audit the prevalence of adrenal masses discovered in all computerised tomography (CT) abdominal imaging done over one calendar month in our centre. A secondary aim was to identify the underlying diagnosis and fate of the discovered adrenal nodules. All 690 CT scans done in March 2011 in our centre that...

ea0025p105 | Clinical biochemistry | SFEBES2011

Review of 125 individuals with adrenal incidentalomas: a single centre cohort

Theodoraki Aikaterini , Khoo Bernard , Perera Sithara , Schwappach Anna , Hamda Arif , Vanderpump Mark , Bouloux Pierre-Marc

Background: Adrenal masses discovered incidentally during imaging studies (adrenal incidentalomas – AIs) are common and prompt investigations to exclude secretory lesions and malignancy. Uncertainty exists over the best management strategy of AI.Objective: To monitor the current practice against the local protocol and existing guidelines; to identify the biochemical and imaging outcomes in a single centre cohort.Methods: Retro...

ea0013p198 | Endocrine tumours and neoplasia | SFEBES2007

An unusual phaeochromocytoma crisis presenting with profound hypoglycaemia and subsequent hypertension

Davis Katherine , Khoo Bernard , Drake William M , Grossman Ashley B , Frankton Sarah

A 47 year old Macedonian Personal Trainer presented with 4 days of vomiting, abdominal pain and profuse sweating. He admitted abusing anabolic steroids 20 years previously but never insulin. The presenting capillary blood glucose (CBG) was 1.7 mmol/L, blood pressure (BP) 182/106 mmHg, pulse 62 bpm. On examination, he was sweaty, pale and cold. Blood was drawn for measurement of insulin, C-peptide, glucose, cortisol and thyroid function tests. He was treated with 50% dextrose a...