Searchable abstracts of presentations at key conferences in endocrinology

ea0050s5.3 | Beyond paragangliomas | SFEBES2017

Surveillance imaging strategies in SDHx

Akker Scott

The increased testing for key genes associated with familial paraganglioma syndromes has, in turn, led to a rapid increase in the identification of asymptomatic carriers through cascade screening. Mutations in SDH subunits B and D account for approximately 50% of the ‘gene positive’ index case results, yet there remains significant controversy and variability with respect to the screening strategies for their asymptomatic relatives. For SDHD at risk carriers, surveil...

ea0050s5.3 | Beyond paragangliomas | SFEBES2017

Surveillance imaging strategies in SDHx

Akker Scott

The increased testing for key genes associated with familial paraganglioma syndromes has, in turn, led to a rapid increase in the identification of asymptomatic carriers through cascade screening. Mutations in SDH subunits B and D account for approximately 50% of the ‘gene positive’ index case results, yet there remains significant controversy and variability with respect to the screening strategies for their asymptomatic relatives. For SDHD at risk carriers, surveil...

ea0082wd14 | Workshop D: Disorders of the adrenal gland | SFEEU2022

Adrenal insufficiency after unilateral adrenalectomy for Cushing”s Syndrome

Subramaniam Yuvanaa , Akker Scott

We present a 38-year-old patient who had adrenal insufficiency following laparoscopic removal of 3.2 cm cortisol-secreting right adrenal tumour. His biopsy showed adrenocortical adenoma in keeping with Cushing’s syndrome. He had a history of hypertension with suboptimal control despite being on 3 anti-hypertensives. His early morning cortisol (by GP to investigate secondary causes) were elevated and this prompted Endocrine referral. Clinical history and examination were ...

ea0082wh4 | Workshop H: Miscellaneous endocrine and metabolic disorders | SFEEU2022

Severe hyponatraemia related to ACTH deficiency and SIADH from lymphocytic hypophysitis

Subramaniam Yuvanaa , Akker Scott

A fit and well 41-year-old lady who was 10-days post-partum was referred to our Endocrine team for hyponatraemia (serum sodium 117 mmol/l). She had a spontaneous vaginal delivery but had 1.5L blood loss due to difficulty with placenta removal. Her baby is well with no medical issues. During pregnancy, she was started on aspirin due to maternal age and had diet-controlled gestational diabetes. She presented to hospital with extreme lethargy. She also reported lightheadedness a...

ea0104p6 | Adrenal & Cardiovascular | SFEIES24

Benefits of medical therapy with alpha-adrenergic inhibition pre-operatively for secretory paragangliomas – more than just blood pressure control

Tufton Nicola , Akker Scott

Many symptoms of phaeochromocytomas and paragangliomas (PPGL) are due to the effects of excess catecholamines. Catecholamines exert their effect on alpha- and beta-adrenergic receptors. Before patients undergo curative surgery, guidelines recommend medical management is commenced to provide cardiovascular stability. This blockade allows restoration of normotension and normal circulating volume (reducing the risks of an intraoperative hypertensive crisis and postoperative hypot...

ea0055p28 | Poster Presentations | SFEEU2018

Eponymous mischief: A syndrome within a syndrome

Tufton Nicola , Cross Susan , Akker Scott

Case history: A 32 year old male diagnosed with McCune-Albright syndrome aged 18, presented with a painful left knee and difficulty in walking, limiting his usual activities. He was diagnosed with Acromegaly (IGF-1 451 ng/ml, mean GH 2.71 ug/L) aged 26 years and had multiple sites of fibrous dysplasia, causing bone pain. On examination he had tall stature and features of acromegaly with normal visual fields and palpable masses behind his left knee and upper thigh.<p class=...

ea0055wh2 | Workshop H: Miscellaneous endocrine and metabolic disorders | SFEEU2018

An unexpected cause of hypoglycaemia post-bariatric surgery

O'Toole Sam , Coppack Simon , Akker Scott

Case history: A 54 year-old gentleman was transferred as an inpatient from another centre for investigation and management of refractory hypoglycaemia following a revision gastric bypass. He was requiring a continuous infusion of 20% dextrose on transfer to maintain normoglycaemia. He had a complex bariatric surgical history dating back 7 years. His initial procedure had been a sleeve gastrectomy that was subsequently converted to a gastric bypass which had then been reversed ...

ea0082p18 | Poster Presentations | SFEEU2022

A case of Severe and Chronic Vitamin D Toxicity: when all treatment options are exhausted

Mansukhbhai Shekhda Kalyan , Akker Scott , Rathore Ali

Case History: A 68-year-old gentleman was admitted to the hospital following a history of weight loss, lethargy, tiredness for about 6 months. His past history includes hiatus hernia, esophagitis and kidney stones. He reported taking over the counter vitamin D (60,000 IU daily) for more than 2 years. He was not on any other regular medications.Investigations: His initial investigations showed acute kidney injury with severe PTH independent hypercalcaemia...

ea00100wd4.3 | Workshop D: Disorders of the adrenal gland | SFEEU2024

A case of phaeochromocytoma-optimisation of alpha and beta blockage

Thinn Yu Thinn , Akker Scott , Parvanta Laila

A 42-year-old man from Colchester was referred to our endocrinology service in January 2023. He was having abdominal pain for a year, unresponsive to a trial of PPI. He was also found to have hypertension for one year which was controlled by Amlodipine. An ultrasound organised by his GP revealed gallstones and a substantial right supra-adrenal mass, leading to a referral to the local urology team. Subsequently, CT scan was performed which characterised as a likely phaeochromoc...