Searchable abstracts of presentations at key conferences in endocrinology

ea0034p147 | Clinical practice/governance and case reports | SFEBES2014

Non islet cell tumour hypoglycaemia: management strategies for a rare and challenging condition

Kalathil Dhanya , Roughneen Simon , Shah Momin , Akram Ali , Zaidi Reza , Purewal Tejpal , Ahmad Aftab , Weston Philip

We previously reported a case of non islet cell tumour hypoglycaemia (NICTH) due to increased ‘big’-IGF2 production in a lady with haemangiopericytoma (HAP). We now describe the challenges in managing this lady who had recurrent, disabling hypoglycaemia requiring frequent hospitalisation.This patient presented with symptomatic hypoglycaemia 15 years after the diagnosis of parasaggital HAP. At presentation she had tumour recurrence with liver an...

ea0021p202 | Endocrine tumours and neoplasia | SFEBES2009

A rare case of steroid responsive non-islet cell tumour hypoglycemia (NICTH) secondary to metastatic haemangiopericytoma

Mon Aung , Ahluwalia Rupa , Tehseen Saffia , Rathore Ali , Weston Philip , Ahmad Aftab

Introduction: Spontaneous hypoglycaemia is very rarely related to non-islet cell tumours. Most of them are due to mesenchymal tumours including haemangiopericytoma (HAP). It has been reported that, in patients with NICTH who have inoperable tumours, high doses of glucocorticoid or recombinant human growth hormone may be effective in treating hypoglycaemia. We present, with relevant imaging, a rare case of metastatic HAP causing an increased level of insulin like growth factor ...