Searchable abstracts of presentations at key conferences in endocrinology

ea0034p175 | Neoplasia, cancer and late effects | SFEBES2014

Adrenocortical cancer: rare but gloomy cause of adrenal lesions

Falinska Agnieszka , Vakilgilani Tanaz , Woods David , Ling Yong Yong , Tanday Raj , Todd Jeannie F

We present a case of 50-year-old female who presented to a local hospital with sudden onset severe sharp left flank pain. Urgent CT revealed a mass in the left adrenal gland which was thought to be a supra-renal bleed. It measured 6 cm at this point. She was discharged with paracetamol and re-assured. As she was not feeling well, she had an US kidney in private sector 1 month later revealing static appearance of presumed haematoma. Following the period of observation to allow ...

ea0034p176 | Neoplasia, cancer and late effects | SFEBES2014

Metastatic paraganglioma with unknown genetics: to screen or not to screen the family?

Falinska Agnieszka , Vakilgilani Tanaz , Woods David , Tanday Raj , Yong Ling Yong , Todd Jeannie F

We present a family of a 45-year-old patient who presented to hospital acutely unwell with metastatic paragangliomas. Unfortunately due to rapidity of his presentation, no genetic testing was performed. He was found to have 5 cm right carotid body tumour. His urine collections confirmed raised (seven times normal) 24 h urine metanephrines 24.55 μmol (normal <3.47 μmol). Shortly after the initial diagnosis he was found to have extensive vertebral body metastases i...

ea0034p177 | Neoplasia, cancer and late effects | SFEBES2014

Clinical dilemmas in diagnosing pheochromocytoma

Falinska Agnieszka , Vakilgilani Tanaz , Tanday Raj , Ling Yong Yong , Todd Jeannie F

A 43-year-old gentleman was referred from a local hospital with biochemical and radiological suspicion of pheochromocytoma. He admitted to a 10-year history of palpitations, flushing, sweating, and tremors. He was intermittently feeling stressed, anxious and angry with mood swings. He had difficulty sleeping and suffered from headaches. He was treated for hypertension and 10 years prior he was admitted to the local hospital with malignant hypertension. He was drinking up to 40...

ea0034p293 | Pituitary | SFEBES2014

GH excess of unknown origin

Falinska Agnieszka , Ling Yong Yong , Tanday Raj , Vakilgilani Tanaz , Todd Jeannie F

A 68-year-old patient was noted to have prognathism, broad fingers and toes and coarse facial features during her admission for a hip replacement 2 years ago. Her family noted change to her facial features and she admitted to increase in her shoe size over 10 years. Her past medical history included treated hypertension only. Her oral glucose tolerance test (OGTT) confirmed paradoxical rise of GH with peak 6.23 μg/l. Her initial IGF1 was raised at 131 nmol/l (6–30 nm...