SFEBES2007 Poster Presentations Clinical practice/governance and case reports (98 abstracts)
St.Peters Hospital, Chertsey, United Kingdom.
A 75-year old gentleman presented with symptoms of increasing lethargy, loss of appetite associated with weight loss and constant micturition. A CT scan showed extensive peritoneal mass in the lower abdomen and pelvis with disseminated intraperitoneal malignancy. A CT guided biopsy confirmed a poorly differentiated tumour. Immunohistochemistry showed that all the cytokeratin markers were negative, but vimentin was positive and CD117 (c-kit) was strongly positive, indicating that it was a malignant GIST. In the following two weeks, the patient experienced recurrent episodes of blackouts associated with excessive sweating and was admitted to hospital. The patient showed a suboptimal response to short synacthen test. Blood tests during an episode of spontaneous hypoglycaemia revealed.
Investigations | Results | Normal range |
Blood glucose | 1.4 mmol/L | 46.4 |
Insulin | 12 pmol/L | 0180 |
C-peptide | 154 pmol/L | 180630 |
ACTH | 20 ng/L | 050 |
Cortisol | 248 nmol/L | Reduced response to a glucose of 1.4 mmol/L |
Growth hormone | 4.6 mu/L | 05 |
IGF I | 2.9 nmol/L | 636 |
IGFII | 61.7 nmol/L | 37.282.1 |
IGF II:IGF I ratio | 21.3 | <10 |
While on the ward, he had recurrent episodes of spontaneous hypoglycaemia requiring correction with 10% dextrose infusion. There was no improvement in blood sugars despite treatment with hydrocortisone and octreotide. As an elevated IGF II:IGF I ratio confirmed the diagnosis of non-islet cell hypoglycaemia, the patient was commenced on Growth hormone 0.02 mg/kg subcutaneously daily with successful stabilization of blood sugars.