Searchable abstracts of presentations at key conferences in endocrinology

ea0050cmw5.5 | Workshop 5: How do I. . . (2) | SFEBES2017

How do I manage hypercalcaemia during pregnancy?

Sam Amir

Hypercalcaemia due to primary hyperparathyroidism during pregnancy may be associated with maternal and foetal complications as well as neonatal tetany. Asymptomatic women with mild hypercalcaemia may be managed conservatively. Symptomatic patients or those with severe hypercalcaemia should be offered parathyroidectomy in the second trimester. This session will summarise the current practice in the management of patients with hypercalcaemia during pregnancy at Hammersmith Hospi...

ea0050cmw5.5 | Workshop 5: How do I. . . (2) | SFEBES2017

How do I manage hypercalcaemia during pregnancy?

Sam Amir

Hypercalcaemia due to primary hyperparathyroidism during pregnancy may be associated with maternal and foetal complications as well as neonatal tetany. Asymptomatic women with mild hypercalcaemia may be managed conservatively. Symptomatic patients or those with severe hypercalcaemia should be offered parathyroidectomy in the second trimester. This session will summarise the current practice in the management of patients with hypercalcaemia during pregnancy at Hammersmith Hospi...

ea0044cmw3.5 | Workshop 3: How do I… | SFEBES2016

How do I prepare a patient for phaeo surgery?

Sam Amir

All patients with phaeochromocytoma should undergo surgical resection by an experienced surgeon. Surgery should only be carried out after adequate medical preparation to minimize catecholamine-related adverse events. Pre-operative pharmacologic treatment is aimed at controlling hypertension and tachycardia, and volume expansion. This session will summarise the current practice in the medical management of patients with phaeochromocytoma at Hammersmith Hospital....

ea0055wh3 | Workshop H: Miscellaneous endocrine and metabolic disorders | SFEEU2018

Somatostatin analogue therapy in a patient with von Hippel-Lindau disease and multiple pancreatic neuroendocrine tumours

O'Toole Sam , Drake William

Case history: An 11 year old girl was diagnosed with von Hippel-Lindau disease (VHL) on cascade genetic screening due to a positive family history and was enrolled in a VHL surveillance programme. She developed bilateral phaeochromocytomas and underwent staged bilateral adrenalectomies at the age of 12 and 14. At the age of 16, she was discovered to have a 2.5 cm tail of pancreas pancreatic neuroendocrine tumour (pNET) on routine surveillance imaging. This enlarged during foll...

ea0099ep447 | Thyroid | ECE2024

Hypothyroidism and bilateral foot droop

Nagarajah kalyani , Rice Sam

Introduction: Hypothyroidism and hyperthyroidism are commonly encountered medical disorders that can be associated with neurologic and neuromuscular dysfunction. Muscle involvement is a common manifestation of both clinical and subclinical hypothyroidism, although this may not always be clinically appreciated. Hypothyroid associated myopathy can cause weakness, cramps, aching and painful muscles, sluggish movements and Severe myopathy secondary to hypothyroidism leading to Rha...

ea00100p3 | Poster Presentations | SFEEU2024

An interesting case of hypothyroidism: hypothyroidism with bilateral foot drop

Nagarajah Kalyani , Rice Sam

Here we present a 49 year-old-male patient with known T1DM, hypothyroidism on Levothyroxine, with previous history of poor compliance with his Levothyroxine. He was admitted with 3 days history of bilateral feet swelling and foot droop. Following the improvement of his leg swellings, his bilateral foot droop became more prominent. He was diagnosed with Hashimoto hypothyroidism with anti TPO ab levels of 279 IU/Ml (reference range: <34 IU/ml) in 2012. His regular medication...

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 ...

ea0051p058 | Pituitary and growth | BSPED2017

Growth hormone treatment in children: an audit of compliance with NICE Guidance

Sotiridou Ellada , Gorman Sam , Williams Rachel

Background: In the UK, Growth Hormone (GH) is indicated for treatment of children with short stature secondary to growth hormone deficiency (GHD), Prader Willi syndrome (PWS), Turner syndrome (TS), SHOX gene mutation, chronic renal insufficiency and born small for gestational age (SGA).Objectives: The aim was to assess the compliance of our local practice with the NICE guidance for GH therapy in children in addition to local guidance that TFTs and IGF-I ...

ea0051p080 | Diabetes | BSPED2017

School based management of type 1 diabetes in Northern Ireland: A parent’s perception

Ethell Sam , Millar Sarinda , Liana Shifa

Type 1 diabetes is a significant condition affecting school aged children with an increasing incidence in the UK. The effects of a chronic condition such as diabetes on a child can be dramatic and are particularly evident within the school setting. The impact of this condition can also be seen on parents, affecting their career, income and quality of life. Hence, this audit aims to identify the difficulties encountered by children in mainstream education, the impact of school ...

ea0025p143 | Diabetes, metabolism and cardiovascular | SFEBES2011

Insulin-mediated pseudoacromegaly

Sam Amir , Tan Tricia , Meeran Karim

Patients with acromegaly have characteristic clinical features of soft tissue overgrowth. Both somatic and metabolic features of acromegaly are secondary to excess GH secretion and high circulating levels of insulin-like growth factor 1 (IGF1). However, an acromegaloid phenotype associated with severe insulin resistance is occasionally seen in the absence of biochemical hallmarks of acromegaly (insulin-mediated pseudoacromegaly). Here we present a case of ‘insulin-mediate...