Insulin Autoimmune syndrome is a very rare endocrinal disease characterized by repeated hypoglycemia in the presence of elevated serum insulin and positive insulin autoantibodies, in the absence of administration of exogenous insulin, commonly patients with insulin autoimmune syndrome will be harboring other autoimmune diseases that could be active clinically or inactive and only diagnosed by positive serological markers.
In this chapter, we will discuss two clinical cases followed
by discussions and my personal clinical approach in the absence of guidelines.
Due to the disease's rarity, Hirata disease is frequently
misdiagnosed, which exposes patients to needless testing and surgery. Hirata
disease is an insulin autoimmune disease marked by non-exogenous
hyperinsulinemic postprandial hypoglycemia caused by elevated insulin
autoimmune antibodies (IAS), without exogenous insulin and without pathological
abnormalities of pancreatic islets cells.
The disease is uncommon in non-Asian populations, among the
Caucasian population, most of the cases are due to drug exposure, autoimmune
diseases or hematological malignancies, sometimes Hirata disease can be triggered
by viral infection.
In this manuscript, we presented a case of autoimmune
insulin hypoglycemia, the patient was subjected to a few unnecessary
investigations before reaching the correct diagnosis, we reviewed the recent
literature about autoimmunity of endogenous insulin hypoglycemia, we also will
suggest the best practice based on our experience given that there are no
guidelines to follow due to the rarity of the disease. Autoimmune insulin
syndrome and insulin syndrome type B should be in the differential diagnosis of
hyperinsulinemia hypoglycemia, and should be ruled out before proceeding with
any expensive investigations or surgery.
Author (s) Details
Adel Ekladious
Acute Medical Unit, Canberra Hospital, ACT Health, Australia, University of
Western Australia, Australia and Australian National University, Australia.
Please see the book
here:- https://doi.org/10.9734/bpi/mria/v7/321
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