Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep751 | Pituitary and Neuroendocrinology | ECE2023

Every post op hyponatremia is not a SIADH; missed case of hypopituitarism after TBI

Azad Fatima , Meeking Darryl

Introduction: The incidence of hospitalised and fatal traumatic brain injury(TBI) is 235/100 000 with an average mortality rate of 15/100 000. A meta-analysis from 19 studies showed a prevalence of hypopituitarism after TBI of 27.5%.Case report: We report case of 72-year-old man, who suffered traumatic brain injury in October 2021, sustaining multiple skull fractures, with traumatic subarachnoid haemorrhage and subsequent pneumocephalus. He underwent bur...

ea0021p245 | Pituitary | SFEBES2009

Lymphocytic hypophysitis or Sheehan's syndrome?

Partridge Helen , Meeking Darryl

A 34-year-old lady attended clinic-requesting information on recombinant prolactin to assist with breast feeding as she was 32 weeks gestation with her third pregnancy having failed to lactate after her first two pregnancies.In 2003 she developed pre-eclampsia during her first pregnancy and required delivery by Ventouse extraction. She had a significant post-partum haemorrhage of 1200 mls with haemoglobin 7g/dl but no evidence of cardiovascular compromis...

ea0050p060 | Bone and Calcium | SFEBES2017

Review of parathyroid imaging and subsequent surgical findings in primary hyperparathyroidism – do they correlate?

Whicher Clare Alexandra , Karathanasi Eleni , Meeking Darryl

Introduction: Primary hyperparathyroidism is the most common cause of hypercalcemia in the ambulatory setting. Once the diagnosis has been confirmed, imaging of the parathyroid glands is performed locally with a combination of ultrasound scan (USS) and sestamibi/single-photon emission computed tomography (SPECT CT) to localise a parathyroid adenoma prior to surgery.Method: Data was collected on patients undergoing parathyroid surge...

ea0050p060 | Bone and Calcium | SFEBES2017

Review of parathyroid imaging and subsequent surgical findings in primary hyperparathyroidism – do they correlate?

Whicher Clare Alexandra , Karathanasi Eleni , Meeking Darryl

Introduction: Primary hyperparathyroidism is the most common cause of hypercalcemia in the ambulatory setting. Once the diagnosis has been confirmed, imaging of the parathyroid glands is performed locally with a combination of ultrasound scan (USS) and sestamibi/single-photon emission computed tomography (SPECT CT) to localise a parathyroid adenoma prior to surgery.Method: Data was collected on patients undergoing parathyroid surge...

ea0025p87 | Clinical biochemistry | SFEBES2011

A case of complete androgen insensitivity syndrome (CAIS), late presentation and difficult management

Mongolu Shiva , Bujanova Jana , Meeking Darryl

Introduction: Complete androgen insensitivity syndrome (CAIS) is an X-linked genetic disorder characterised by normal female appearance, including external genitalia and the presence of 46XY karyotype. We report a case of CAIS, diagnosed in adulthood, and discuss ethical issues surrounding the disclosure of diagnosis and associated difficulties in further management.Case history: A 33-year-old Nigerian lady was referred to our endocrine service with Prim...

ea0015p44 | Clinical practice/governance and case reports | SFEBES2008

A case of insulinoma presenting with low serum insulin levels

Atkin Marc , Meeking Darryl , Medbak Sami

Insulinoma is a rare but potentially treatable cause of hypoglycaemia. We present a case where achieving a diagnosis of insulinoma was complicated by evidence of low serum insulin levels during documented biochemical hypoglycaemia.A 58 year old lady presented with weight gain and daily episodes of shaking, hot flushes and disorientation that were relieved by the ingestion of food. During symptomatic episodes home capillary blood glucose measurements sugg...

ea0015p184 | Endocrine tumours and neoplasia | SFEBES2008

A case of ‘pseudophaeochromocytoma’: a noradrenaline reuptake disorder

Simon Godwin , Litwic Anna , Meeking Darryl

A 12-year-old girl presented with dizziness, palpitations, headaches and sweating associated with hypertension (170/100 mmHg) and tachycardia (180 beats per minute). Repeated urinary and serum catecholamines were initially unremarkable. Routine biochemical and haematological testing was normal as were serum gut peptides. The patient was commenced on phenoxybenzamine, nifedipine and propranolol. This improved her symptoms, and corrected her tachycardia and raised blood pressure...

ea0063gp10 | Adrenal and Neuroendocrine - Tumour | ECE2019

Brown fat proliferation- A rare complication of Phaeochromocytoma

Sim Sing Yang , Haider Najaf , Meeking Darryl , Flowers David

Phaeochromocytoma is a catecholamine producing tumour arising from the adrenomedullary chromaffin cells. It produces hormones such as epinephrine, norepinephrine, catecholamine and dopamine. (1) There have been some case reports describing an association between Brown adipose tissue (BAT) accumulation due to catecholamine excess caused by a phaeochromocytoma. We present a similar case in this abstract. A 77 year old lady was referred to the community geriatricians with symptom...

ea0021p10 | Bone | SFEBES2009

Recurrence of spontaneously resolving hypercalcaemia, an unusual case

Jaleel Nihad , Meeking Darryl , Albon Lorraine , Chong Lina

A 67-year male presented to his GP with polydypsia, ployuria and bone pains. Routine blood tests showed hypercalcemia (corrected calcium 2.77 mmol/l). Patient was otherwise well. He had a history of ethanol abuse, hypertension and gout.Medications: Allopurinol, ramipril simvastatin and co-dydramol. Repeat blood tests after 4 weeks show a rising calcium of 3.24 mmol/l with intact PTH 33.6 pmol/l (<6.4). He was referred to our endocrinology department ...

ea0021p49 | Clinical practice/governance and case reports | SFEBES2009

Severe hypoglycaemia leading to death in a patient with type 2 diabetes: insulinoma, sulphonylurea overdose or some other cause?

Pui Lin Chong Lina , Jaleel Nihad , Meeking Darryl

We present a 52-year-old lady with type 2 diabetes mellitus, referred by her GP with poor glycaemic control. Her past medical history included haemochromatosis, undifferentiated connective tissue disorder, depression, hypothyroidism, pernicious anaemia and alcohol abuse. Relevant medications were metformin 1 g bd, novorapid 28 units tds, levemir 30 mg od and prednisolone 5 mg od. Her HbA1c was 8.1%, renal function and baseline pituitary function was normal. Following an admiss...