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Endocrine Abstracts (2014) 36 OC7.4 | DOI: 10.1530/endoabs.36.OC7.4

BSPED2014 Oral Communications Oral Communications 7 (5 abstracts)

Hyperosmolar hyperglycaemic state: an unusual presentation of type 2 diabetes mellitus in children

Prabhakaran Kalaivanan 1 , David Inwald 2 , Kumar Somasundaram 3 & Joseph Raine 1


1Whittington Health NHS Trust, London, UK; 2St Mary’s Hospital, London, UK; 3East Surrey Hospital, Redhill, UK.


Background: Hyperosmolar hyperglycaemic state (HHS) is a life-threatening condition that can be the initial presentation of type 2 diabetes mellitus. This condition is characterized by severe hyperglycaemia, a high serum osmolality and dehydration without accumulation of ketoacids. We report two patients who presented with mixed features of HHS and DKA.

Case 1: An 11-year-old Afro-Caribbean boy with severe developmental delay presented with a 4-week history of polyuria, polydipsia, and drowsiness. Investigations showed severe hyperglycaemia (blood glucose 100 mmol/l), hyperosmolar dehydration (corrected Na 197 mmol/l) metabolic acidosis (pH 7.04, base excess −15.4 mmol/l) and renal failure (urea 40 mmol/l and creatinine 310 μmol/l). HbA1c was 9.8% with blood ketones of 5.4 mmol/l. The patient’s clinical course was complicated by multiorgan failure and rhabdomyolysis requiring ventilation, inotropes, and haemofiltration. He was rehydrated and required i.v. insulin for 2 weeks. GAD and insulin antibodies were negative. There was a strong family history of type 2 DM. His HbA1c normalised (5.4%) 5 weeks later. His diabetes remains diet controlled.

Case 2: 17-year-old girl with Wolf–Hirschhorn syndrome presented in an obtunded state. She had a 2-week history of polyuria, polydipsia and sudden deterioration with drowsiness and agitation. Investigations showed blood glucose >40 mmol/l, corrected Na 187 mmol/l, metabolic acidosis (pH 7.20, base excess of −10.4 mmol/l), and renal failure (urea 30 mmol/l and creatinine 163 μmol/l). HbA1c was 10.5% with moderate ketonuria (3+). She required high dependency care and received i.v. insulin for 2 days and her hypernatraemic dehydration resolved slowly over the next 3 days. Her antibodies were negative. She was discharged 2 weeks on dietary treatment alone.

Conclusion: Children with type 2 diabetes can present with features of HHS and DKA. Learning difficulties and co-morbidities may lead to a delay in presentation and more severe illness. HHS can result in profound hyperglycaemia, hypernatraemia, and severe dehydration and may require intensive care.

Volume 36

42nd Meeting of the British Society for Paediatric Endocrinology and Diabetes

British Society for Paediatric Endocrinology and Diabetes 

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