ISSN 1470-3947 (print) | ISSN 1479-6848 (online)

Endocrine Abstracts (2014) 34 P245 | DOI: 10.1530/endoabs.34.P245

Case report: the role of somatostatin analogue therapy in nesidioblastosis following Roux-en-Y bypass surgery

Rajamani Manikandan, Shiva Mongolu & Azraai Nasruddin


University Hospital Southampton, Southampton, UK.


Background: Postprandial hyperinsulinemic hypoglycaemia due to nesidioblastosis is a significant and debilitating complication after Roux-en-Y gastric bypass surgery (RYGB). There is growing evidence suggesting this is due to increased incretin hormones secretion. Nesidioblastosis can be difficult to manage with variable response to different pharmacological therapies and some requiring partial/total pancreatectomy or revision of bypass surgery pouch. We present a patient who has had partial response to octreotide.

Case report: A 45-year-old lady had RYGB 18 months ago for significant reflux symptoms. She also lost 35 kg but developed severe postprandial neuroglycopenic symptoms that occurred 90–120 min after meals. She gained 10 kg. During oral glucose tolerance test (OGTT) her blood glucose dropped to 1 mmol/l at 90 min with insulin 11.1 μu/l and C-peptide 2595 pmol/l. She did not have any benefit from dietetic advice, low GI diet, acarbose, and Guar gum. Pancreatic CT scans and calcium stimulation test did not localize a cause for her hyperinsulinemia. Her symptoms improved partially with diazoxide but it was withdrawn due to side effects. Repeating OGTT on diazoxide, her glucose dropped to 1.4 mmol/l in 90 min with peak insulin 158.1 μu/l and peak C-peptide 5826 pmol/l. Her symptoms improved with octreotide 50 μg TDS. OGTT done after 6 months on octreotide therapy showed peak glucose of 14.9 mmol/l at 90 min with blunted insulin response with peak levels of 33.5 μu/l. However, she continued to report intermittent postprandial hypoglycaemia. We switched her to octreotide LAR but hypoglycaemia got worse.

Discussion: Our case highlights the difficulties in managing the symptoms of nesidioblastosis. Subcutaneous octreotide worked well initially but the effects became attenuated. Her symptoms could be episodes of rebound hypoglycaemia when octreotide effect wore off. It is unclear why octreotide LAR did not work. Pasireotide with its potent suppression of incretin release is likely to work well. We have obtained funding for a trial of pasireotide therapy.

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