Searchable abstracts of presentations at key conferences in endocrinology

ea0016p281 | Endocrine tumours | ECE2008

An unusual case of painful gynaecomastia due to large adrenocortical tumour

Lakshmi Santhosh , Foote John

We present an unusual case of painful gynaecomastia due to a large adrenocortical tumour secreting oestradiol and other steroid hormones.A 46 years old man presented with a 6 months history of progressive, painful gynaecomastia. He had no other specific symptoms and had previously been well. Alcohol intake was not excessive. Interestingly, his sister had presented with a phaeochromocytoma 2 years previously.Examination demonstrated...

ea0021p92 | Clinical practice/governance and case reports | SFEBES2009

A case of spontaneously resolving occult ectopic ACTH-dependent Cushing's syndrome

Browne Duncan , Foote John , Fox Thomas

A 70-year-old woman was referred to the endocrine clinic with recently diagnosed diabetes mellitus and poorly controlled systemic hypertension. At presentation she had clinical features of Cushing’s syndrome including central obesity, Cushingoid facies and marked proximal myopathy. BP was 220/190. Initial biochemistry revealed plasma sodium 140 mmol/l, potassium 3.6 mmol/l and creatinine 82 mmol/l. Overnight 1 mg dexamethasone suppression test revealed cortisol 1148 mmol/...

ea0028p68 | Clinical practice/governance and case reports | SFEBES2012

Acute presentation of ectopic Cushing’s syndrome due to Phaeochromocytoma co-secreting ACTH

Kankara ChenchiReddy , Creely Steven , Foote John , Dugal Tabinda

We present a case of Phaeochromocytoma co-secreting ACTH as a rare cause of Cushing’s syndrome. Our patient is a 49 year lady admitted acutely with sudden onset headache and severe hypertension. CT brain and CSF analysis were normal. Her urinary catecholamines were found to be elevated. Noradrenaline 709 and 972 nmol/ mmol of creatinine (ref range 0–48), Adrenaline 215 and 256 (ref range 0–10). CT abdomen revealed 4.2 cm left adrenal mass, MIBG scan confirmed ph...

ea0021p91 | Clinical practice/governance and case reports | SFEBES2009

Failure of renin determined by immunoassay to suppress in a case of adrenocortical carcinoma secreting excess mineralocorticoid

Fox Thomas , Mihai R , Fisher Roy , Foote John

A 48-year-old woman presented to her GP with polyuria and proximal muscle weakness. She was found to have newly developed hypertension at 180/96 and her serum potassium was 2.7 mmol/l. Lisinopril 40 mg od and Slow-K 1 tablet bd were started and she was referred for further investigation.On clinic review blood pressure was 188/110 supine and 190/110 standing. Serum sodium was 147 mmol/l, potassium 3.7 mmol/l and total bicarbonate 29 mmol/l. Her Lisinopril...

ea0015p341 | Thyroid | SFEBES2008

Specialist endocrine care for all hyperthyroid patients?

Evans Kate , Coupe Aileen , Mascas Ramona , Pilianidis George , Foote John , Browne Duncan , Pinkney Jon

Objectives: To establish the proportion of patients locally with potentially significant thyroid pathology not receiving specialist endocrine input. To look at the management of hyperthyroid patients within the Endocrinology service.Patients and methods: Utilising the laboratory database, 121 patients identified (97 female, 24 male; age range 17–93 years, average 55 years) with TFTs suggesting hyperthyroidism (raised fT4/fT3, and/or suppressed TSH) ...