Authors

BUNYAMIN AYDIN1, OGUZHAN AKSU1, MEHMET NUMAN TAMER1, BANU KALE KOROGLU1, AYSE YIGIT2

Departments

1Suleyman Demirel University, Faculty of Medicine, Department of Internal Medicine, Division of Endocrinology and Metabolism 2Suleyman Demirel University, Department of Medical Biology and Genetics, Isparta, Turkey

Abstract

Insulin Autoimmune Syndrome (IAS) is a rare cause of hypoglycemia. We present the case of a 54-year-old male patient who was admitted to the emergency department with blurred consciousness approximately 6 weeks after the initiation of the methimazole therapy due to the diagnosis of Graves’ disease. The blood glucose level was 40 mg/dL and levels of fasting insulin, C-peptide, and anti-insulin antibodies were increased. The patient was considered to have IAS and the methimazole therapy was terminated. Following the termination of the treatment, the complaints disappeared and the insulin antibodies gradually decreased to normal levels in approximately 8 months.

Keywords

Hypoglycemia, Insulin autoimmune syndrome, Methimazole

DOI:

10.19193/0393-6384_2016_2_70