Korean J Med.  2009 Apr;76(Suppl 1):S122-S126.

A case of insulin autoimmune syndrome

Affiliations
  • 1Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea. tazzina@paran.com
  • 2Department of Occupational and Environmental Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.

Abstract

Insulin autoimmune syndrome is an uncommon cause of hypoglycemia. According to the type of antibody, it can be classified as caused by insulin or insulin receptor autoantibodies. Generally, insulin autoimmune syndrome develops following exposure to exogenous insulin or sulfhydryl medications, although insulin or insulin receptor antibody may also occur spontaneously. We treated a 54-year-old woman who developed spontaneous hypoglycemia. The patient had repeated hypoglycemia despite the infusion of dextrose solution. Her serum insulin, c-peptide, and insulin autoantibody were elevated, even during the hypoglycemic periods. Insulin receptor autoantibody and HLA-cw4/B62/DR4 were positive. After steroid and diazoxide treatment, the hypoglycemic symptoms improved gradually. No further hypoglycemic episodes occurred after tapering the medication over 1 year. We present a case of insulin autoimmune syndrome with positive insulin and insulin receptor autoantibodies.

Keyword

Hypoglycemia; Insulin autoimmune syndrome; Insulin autoantibody; Insulin receptor autoantibody

MeSH Terms

Autoantibodies
C-Peptide
Diazoxide
Female
Glucose
Humans
Hypoglycemia
Insulin
Middle Aged
Receptor, Insulin
Autoantibodies
C-Peptide
Diazoxide
Glucose
Insulin
Receptor, Insulin
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