Searchable abstracts of presentations at key conferences in endocrinology

ea0074oc10 | Oral Communications | SFENCC2021

An unusual case of raised PTH

Jamsheed Mohammed , Lambert Kimberley

60 year old gentleman referred to endocrine clinic from Rheumatology for raised PTH 23.5 pmol/l, in the context of normal calcium 2.2 mmol/l, low vitamin D 27.3 nmol/l, raised ALP 273 U/l, low phosphate 0.57 mmol/l and normal renal function. Past medical history of hypertension, Barrett’s oesophagus, cluster headaches and previous left femur fracture secondary to motor cross accident. The ALP isoenzyme for bone was raised. He was complaining of backache which he had for s...

ea0015p366 | Thyroid | SFEBES2008

Radioactive iodine (I131) treatment in thyrotoxicosis- audit of local experience

Lambert Kimberley , Al-Mrayat Maen

We reviewed the outcomes of 40 patients (30F, 10M; mean age 56 years) with thyrotoxicosis who were referred for radioactive iodine treatment (RAI) via our department (catchment area of 130 000 people) over a period of 3 years (February 2004–March 2007). Twenty-three patients had Graves (GD); 6 had single toxic adenoma (STA); 11 had toxic multinodular goitre (MNG). Thirty-six patients (90%) had a preceding isotope scan, and 2 patients (5%) had previous partial thyroidectom...

ea0082wh2 | Workshop H: Miscellaneous endocrine and metabolic disorders | SFEEU2022

Postpartum Hyponatremia

El Abd Souha , Parsad Meenakshi , Lambert Kimberley

Background: Severe hyponatremia can be associated with oxytocin infusion. The incidence of hyponatraemia after oxytocin is around 5%. There are reported cases of serious neurological complications including seizures, coma and maternal death.Case report: A 37-year-old female with known partial central diabetes insipidus following a head injury was established on Desmopressin nasal spray 10 mg twice a day. She had an uneventful pregnancy on the same dose. ...

ea0091p8 | Poster Presentations | SFEEU2023

A rare case of FGF23 producing tumour

Munisamy Narmadha , Azman Nur , Lambert Kimberley

Case history: A 67-year-old lady was referred to endocrinology with an 8-year history of mild hyperparathyroidism with Parathyroid hormone of 7.4 -15.3 pmol/l (Normal -1.95-8.49). Her corrected calcium ranged from 2.46-2.66 mmol/l (Normal 2.2 -2.62), phosphate 0.63 -1.0 mmol/l (normal 0.8-1.5), normal renal function and normal vitamin D. Her urine calcium to creatinine ratio was 0.7 mmol/mmol (Normal 0-0.4).Investigations and treatment: She had myalgia d...

ea0059ep115 | Thyroid | SFEBES2018

Case Series of unusual presentations of Thyrotoxicosis

Parsad Meenakshi , King Samuel , Lambert Kimberley

Thyrotoxicosis is a relatively common condition affecting 1–2% of women and 0.1–0.2% of men. Common symptoms are usually straightforward and easily identified. Rarer presenting features such as confusion and headache have been published in the literature as case reports. We hereby report two cases of Graves Thyrotoxicosis presenting unusually and therefore misleading the initial diagnostic pathway. The first case is a 45-year-old female with a 4-day history of headac...

ea0034p30 | Bone | SFEBES2014

An ectopic parathyroid adenoma presenting with reduced conscious level and severe hypertension

Wiebel Rediet , Lambert Kimberley , Nasruddin Azraai

A 77-year-old lady presented with reduced conscious state, dysphasia and profound confusion on a background of behavioural change and anorexia over the previous 10 days. She was previously independent with history of hypertension controlled on atenolol (100 mg). She was significantly hypertensive 200/100. Her serum calcium was elevated at 4.01 mmol/l (2.05–2.60). The serum parathyroid hormone (PTH) was also significantly elevated at 26 pmol/l (0.5–6.4) consistent wit...

ea0028p95 | Clinical practice/governance and case reports | SFEBES2012

Recurrent atypical adrenocorticotrophic hormone (ACTH) secreting carcinoid tumour causing Cushing’s syndrome

Mlawa Gideon , Lambert Kimberley , Norris Andrea , Li Voon Chong Jimmy

Background: Atypical carcinoid tumours are rare which account for about 15% of all carcinoid tumours. Some of those tumours secrete adrenocorticotrophic hormone (ACTH) causing Cushing's syndrome. We present a case which recurred 16 years after being first diagnosed.Case: A 39 years old woman was referred with few months history of weight gain, irregular menstrual periods, muscle aches, difficult going up the stairs, headaches and blurred vision.She was i...

ea0044p28 | Adrenal and Steroids | SFEBES2016

Incidence and outcomes of hormone-secreting adrenal tumours in pregnancy: a UK 4 year prospective cohort study

Quartermaine Georgia , Lambert Kimberley , Rees Kate , Seed Paul , Dhanjal Mandish , Knight Marian , McCance DR , Williamson Catherine

Objective: To examine the monitoring, management and outcomes of adrenal tumours in pregnancy.Design: A national, prospective observational, cohort study over 4 years using the UK Obstetric Surveillance System (UKOSS).Setting: Consultant led obstetric units.Patients: Women with hormone-secreting adrenal tumours (pheochromocytoma, primary aldosteronism or Cushing’s syndrome) diagnosed before or during pre...

ea0091p16 | Poster Presentations | SFEEU2023

Oncocytic parathyroid adenoma presenting with refractory hypercalcaemia and multiple incidental Brown tumours

Azman Nur , Munisamy Narmadha , Le Carpentier Dana , Syed Maria , Spraggs Paul , Li Voon Chong Jimmy , Lambert Kimberley , Parsad Meenakshi

Case History: A 61-year-old Caucasian female from Ukraine presented with severe hypercalcaemia following routine blood tests performed by the GP. She reported symptoms of back pain and joint pains. She had renal stones 10 years prior. No history of thiazide or lithium use. No red flags; no change in appetite or weight loss. There was no familial history of Multiple Endocrine Neoplasia (MEN). Examination of her neck, cardiorespiratory, abdomen and breasts were normal. <p cl...