Searchable abstracts of presentations at key conferences in endocrinology

ea0050ep049 | Clinical Biochemistry | SFEBES2017

‘2’ much of a problem with hypoglycaemia

Sukumar Nithya , Venkataraman Hema , Ayuk John

Background: An 88 year old gentleman was referred to the endocrine team as an inpatient with recurrent episodes of spontaneous hypoglycaemia. These occurred in the early hours of the morning when he was found to be unrousable from sleep. There was no background history of diabetes. He was under the oncology team on this admission with pyrexia post-palliative chemotherapy with trabecitidine. Significant past medical history include metastatic solitar...

ea0050ep049 | Clinical Biochemistry | SFEBES2017

‘2’ much of a problem with hypoglycaemia

Sukumar Nithya , Venkataraman Hema , Ayuk John

Background: An 88 year old gentleman was referred to the endocrine team as an inpatient with recurrent episodes of spontaneous hypoglycaemia. These occurred in the early hours of the morning when he was found to be unrousable from sleep. There was no background history of diabetes. He was under the oncology team on this admission with pyrexia post-palliative chemotherapy with trabecitidine. Significant past medical history include metastatic solitar...

ea0087p6 | Poster Presentations | UKINETS2022

The impact of the COVID-19 pandemic on Neuroendocrine tumour (NET) services and patients in the pandemic recovery period: A quantitative and qualitative analysis

Dabke Tanvi , Finnen John , Munir Alia

Introduction: The COVID-19 pandemic has affected the delivery of NET services and patient care. We retrospectively analysed the recovery of NET service provision over the COVID-19 recovery period 2020-2021.Method: The NET database was searched using 3 NET physician codes. Anonymised data was analysed, including PRRT, MIBG, endoscopy and bronchoscopy rates. In February 2022, patient satisfaction questionnaires were posted out to 87 randomly selected NET p...

ea0091p14 | Poster Presentations | SFEEU2023

Hypercalcaemia and delusions of blood poisoning: a parathyroid adenoma refractory to ultrasound-guided ethanol ablation

Conti Alessandro , Anderson John , Goodchild Emily

Case history: An 85-year-old man with primary hyperparathyroidism, resistant to cinacalcet, presented to hospital with paranoid delusions, weakness, constipation and thirst. His past medical history was of vitamin D deficiency and arthritis of the spine. Regular medications were lansoprazole, senna, and fluticasone nasal spray. He was a never-smoker and had no relevant family history. Neck examination was unremarkable.Investigations: Corrected serum calc...

ea0069p55 | Poster Presentations | SFENCC2020

‘A Case Report on Eruptive Xanthoma as the First Presentation of Undiagnosed Diabetes Mellitus’

Mahmood Taha , Samarasinghe Suhaniya , John Laurence

Case history: A 33 year old gentleman presented with a 4 month history of an evolving rash. This initially appeared on the extensor surfaces of the knees bilaterally and progressed to involve both arms and the trunk. This rash was not associated with fever, pain, pruritis or any other symptoms. These lesions were diffuse erythematous crops of yellow papules visible over the knees, arms and trunk. The patient was initially diagnosed with folliculitis and treated with oral flucl...

ea0065p388 | Reproductive Endocrinology and Biology | SFEBES2019

When dehydration cured Conn’s !

Musharraf Adeel , Ahmad Adeeba , Milles John

62 year-old lady with a long history of hypokalaemia, hypertension and a random aldosterone of 786 pmol/l with suppressed renin of <8.0 mU/l at a time when she was taking Nebivolol, perindopril and Felodipine. Her Hypokalaemia improved after addition of Spironolactone and remained above 3.5 mmol/l. Biochemical work up confirmed a diagnosis of Conn’s syndrome and her BP control improved after addition of Aldosterone antagonist as above. Adrenal MRI revealed a 13 mm adr...

ea0062wa8 | Workshop A: Disorders of the hypothalamus and pituitary | EU2019

Pituitary apoplexy in a non-functioning pituitary adenoma: A case of favorable outcome in conservative management approach

Wijesinghe Achini , Sinha Saurabh , Newell-Price John

Introduction: Pituitary apoplexy presents as a medical emergency, and usually occurs in people with pituitary macroadenomas. Immediate multidisciplinary expertise and timely intervention is needed to mitigate the associated morbidity. There is controversy regarding the role and the timing of neurosurgical intervention versus conservative management approach to obtain best visual and endocrine outcomes. Here we present a case of a man presenting with pituitary apoplexy and mana...

ea0049ep124 | Clinical case reports - Pituitary/Adrenal | ECE2017

An unusual cause of unilateral adrenal haemorrhage

Jayaweera Jayamalee , Symington Emily , Clark John

A 24 year old man was admitted by the Surgeons with left sided abdominal pain. He was febrile and tachycardic and found to have raised inflammatory markers. Abdominal CT scan revealed a 6 cm left adrenal haemorrhage with no evidence of an underlying lesion. Initial endocrine investigations were unremarkable for Cushings, Conn’s and adrenal insufficiency. Norepinephrine levels were high but settled subsequently. He had a coagulopathy and evidence of reactivation of EB viru...

ea0044ep61 | (1) | SFEBES2016

A rare case of Follicular Stimulating Hormone (FSH) secreting pituitary adenoma in male

Kempegowda Punith , Ayuk John , Toogood Andrew

A 61-year-old man presented to his primary care service with complains of frequent hot flushes, dizziness and headache. Following initial screening, an incidental pituitary lesion was diagnosed on computed tomography (CT) scan and hence was referred to specialist review. Further detailed history revealed similar presentation with dizziness and hot flushes two and a half years ago. He was then diagnosed with essential hypertension after a negative work-up for Cushing disease. H...

ea0041gp205 | Thyroid - Translational &amp; Clinical | ECE2016

One in four patients with adequately treated primary hypothyroidism continue to be symptomatic and persisting symptoms related to ongoing thyroid auto-immunity

Jacob Jubbin , Sebastain Ivy , John Mary

Background: A significant percentage of patients with adequately replaced primary hypothyroidism (PH) continue to be symptomatic. Some of these persisting symptoms maybe attributed to non-restoration of neurocognitive functions and psychological well-being.Objectives: To estimate the prevalence of persisting hypothyroid symptoms in patients with PH on biochemically adequate replacement therapy. To correlate persistent symptoms with thyroid hormone levels...