Searchable abstracts of presentations at key conferences in endocrinology

ea0044ep17 | (1) | SFEBES2016

Please don’t operate on this patient - A case of ‘Adrenaline running high’

Khan Irfan , Hasan Faisal , Lonnen Kathryn

Phaeochromocytomas are rare catecholamine secreting tumours arising from the chromaffin cells of the adrenal medulla. The annual incidence is approximately 0.8 per 100,000 person-years. Most of them are sporadic but in about 25–30% of patients, they are part of a familial disorder. The classic clinical features are episodic headache, sweating and tachycardia (with or without hypertension). However, a minority of patients are asymptomatic. We present a clinical case in whi...

ea0050p067 | Bone and Calcium | SFEBES2017

Playing tennis with off the chart Calcium levels !!

Ahmed Shaza , Hasan Faisal , Lonnen Kathryn , Cheyne Elizabeth , Johnson Andrew

Severe Hypercalcaemia can present as a life threatening emergency requiring urgent measures to lower the calcium. Usually, this is associated with Primary Hyperparathyroidism. It can result in obtundation, oliguria, anuria, collapse or arrhythmias. It is important to act fast and decisively to prevent fatal complications.We describe a 39 year old gentleman who was a tennis coach, who was brought after he collapsed in his bathroom. ...

ea0050p067 | Bone and Calcium | SFEBES2017

Playing tennis with off the chart Calcium levels !!

Ahmed Shaza , Hasan Faisal , Lonnen Kathryn , Cheyne Elizabeth , Johnson Andrew

Severe Hypercalcaemia can present as a life threatening emergency requiring urgent measures to lower the calcium. Usually, this is associated with Primary Hyperparathyroidism. It can result in obtundation, oliguria, anuria, collapse or arrhythmias. It is important to act fast and decisively to prevent fatal complications.We describe a 39 year old gentleman who was a tennis coach, who was brought after he collapsed in his bathroom. ...

ea0059ep84 | Neuroendocrinology and pituitary | SFEBES2018

A clinically functioning gonadotroph adenoma presenting with abdominal pain, bilateral multi-cystic ovaries and fibromatosis

Broughton Chloe , Sorour Mohammad , Mears Jane , Williams Adam , Lonnen Kathryn

Introduction: We present the case of a clinically functioning gonadotroph adenoma in a pre-menopausal woman with abdominal pain, bilateral multi-cystic ovaries and fibromatosis. To our knowledge, this is the first case of fibromatosis associated with a functioning gonadotroph adenoma.Case: A 36 year old female presented on three occasions with acute abdominal pain. She was previously well and had two normal pregnancies. On the first admission, she underw...

ea0050ep042 | Clinical Biochemistry | SFEBES2017

A rare cause of acute severe hyponatraemia secondary to the syndrome of inappropraite anti-diuretic hormone (SIADH) secretion

Wordsworth Georgina , Hasan Faisal , Parfitt Vernon , Chau Fong , Cheyne Elizabeth , Tatovic Danijela , Lonnen Kathryn , Johnson Andrew

Hyponatremia is the commonest electrolyte abnormality presenting to Medical Admissions and when acute, severe and symptomatic, is associated with high mortality. The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common underlying disorder in hospitalised patients with euvolaemic hyponatraemia and is a complication of many clinical conditions and drug therapies.We discuss the cases of two patients...

ea0050ep042 | Clinical Biochemistry | SFEBES2017

A rare cause of acute severe hyponatraemia secondary to the syndrome of inappropraite anti-diuretic hormone (SIADH) secretion

Wordsworth Georgina , Hasan Faisal , Parfitt Vernon , Chau Fong , Cheyne Elizabeth , Tatovic Danijela , Lonnen Kathryn , Johnson Andrew

Hyponatremia is the commonest electrolyte abnormality presenting to Medical Admissions and when acute, severe and symptomatic, is associated with high mortality. The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common underlying disorder in hospitalised patients with euvolaemic hyponatraemia and is a complication of many clinical conditions and drug therapies.We discuss the cases of two patients...

ea0077p227 | Neuroendocrinology and Pituitary | SFEBES2021

Ectopic Cushing’s syndrome: challenging the stereotype

Wordsworth Georgina , Talbot Fleur , Cheyne Elizabeth , Chau Fong , Lonnen Kathryn , Tatovic Danijela , Russell Georgina , Kahal Hassan , Parfitt Vernon

Ectopic Cushing’s syndrome (CS) is commonly caused by malignancy, often behaves aggressively and may not clinically manifest with features of hypercortisolism due to its rapid course and associated cachexia. This may mislead clinicians into discounting the diagnosis in patients with more indolent features of CS. We present a 41 year old woman with an 8 year history of Cushingoid features with associated hypertension, obesity and Type 2 Diabetes. Investigations confirmed C...