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Doege-Potters syndrom er en solitær fibrøs tumor associeret med svær hypoglykæmi

Forfatter(e)
Astrid Uttenthal Larsen1 & Hanne Krogh Rose2
1) Medicinsk Afdeling, Regionshospitalet Viborg 2) Kræftafdelingen, Aarhus Universitets-hospital

Ugeskr Læger 2019;181:V02190082
Reference: 
Ugeskr Læger 2019;181:V02190082
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Astrid Uttenthal Larsen & Hanne Krogh Rose:

Doege-Potter syndrome is a solitary fibrotic tumour often leading to hypoglycaemia

Ugeskr Læger 2019;181:V02190082

Doege-Potter syndrome is a rare paraneoplastic syndrome, in which a solitary fibrotic tumour secretes insulin-like growth factor II leading to hypoglycaemia. In this case report, a 70-year-old woman known with a big intra-abdominal tumour was admitted to hospital, unconscious with a blood sugar of 1.8 mmol/l. She was treated with intravenous glucose until surgery, which cured her temporarily. After four months she had relapse and no effect of chemotherapy. Surgery is the only curative treatment for Doege-Potter syndrome, which is important to remember, if a patient has unexplained hypoglycaemia and a tumour.

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