Authors
Yosuke Oshima, Naohiro Saito, Takahisa Kawaguchi, Mikio Okayama, Hiroaki Taguchi, Hideki Orikasa, Takashi Ando
Published in
Internal medicine (Tokyo, Japan). Oct 08, 2026. Epub Oct 08, 2026.
Abstract
We present the case of a 73-year-old man diagnosed with insulin autoimmune syndrome (IAS) during an investigation of hypoglycemia. This disease is a rare cause of hypoglycemia induced by autoantibodies against insulin. The patient was diagnosed with IgG4-related disease (IgG4-RD). Moreover, the patient had myelodysplastic syndrome (MDS). We hypothesized that immunological dysregulation driven by MDS may have contributed to the coexistence of these two rare conditions in our patient. Treatment with prednisolone promptly resolved hypoglycemia and improved the disease activity of IgG4-RD. We present this case as, to the best of our knowledge, it is the first peer-reviewed case report of coexisting IAS and IgG4-RD.
PMID:
42844187
Bibliographic data and abstract were imported from PubMed on 08 Oct 2026.
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