Kosin Medical Journal (Dec 2013)

A Case of Type III Autoimmune Polyglandular Syndrome

  • Sangeon Gwoo,
  • Young Sik Choi,
  • Bu Kyung Kim,
  • Yo Han Park,
  • Keun Tae Kim,
  • Jun Seop Lee

DOI
https://doi.org/10.7180/kmj.2013.28.2.167
Journal volume & issue
Vol. 28, no. 2
pp. 167 – 170

Abstract

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The autoimmune polyglandular syndromes (APS) are groups of syndromes comprising a combination of endocrine and nonendocrine autoimmune diseases. Among of those four types of APS, the main characteristics of the 3 APS are autoimmune thyroid diseases associated to other autoimmune diseases, excluding Addison’s disease. Type 3 APS are also subdivided into 3A, 3B, 3C, and 3D. Recently, we experience a case of APS manifesting 3A, 3C, and 3D subtype. A 28-year-old woman developed type I diabetes. According to her medical history, she had Graves’ disease, vitiligo, auimmune hemolytic anemia and systemic lupus erythematosus (SLE). The antoantibodies associated with Graves’ disease, SLE, and type I diabetes showed positive findings. We report this case with literatures review.

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