An eight-year-old girl with autoimmune polyglandular syndrome type3A that developed during the course of primary Epstein-Barr virus (EBV) infection: clinical implication of EBV in autoimmune thyroid disease

Immunol Med. 2020 Mar;43(1):57-60. doi: 10.1080/25785826.2019.1701365. Epub 2019 Dec 18.

Abstract

An eight-year-old girl was admitted for prolonged fever and general fatigue. Bilateral reddened and swollen tonsils covered with white fur and increased numbers of atypical lymphocytes in blood led to a diagnosis of infectious mononucleosis (IM) due to primary Epstein-Barr virus (EBV) infection, which was confirmed by a positive anti-EBV viral capsid antigen IgM antibody reaction. She had a swollen thyroid gland and glycosuria at admission, which persisted after IM resolved. Undetectable thyroid-stimulating hormone (TSH), increased thyroid hormone and elevated HbA1c levels led to a diagnosis of autoimmune polyglandular syndrome type3A, based on the presence of antibodies for TSH receptor and glutamic acid decarboxylase. The clinical significance of EBV infection in the development of autoimmune endocrine disorders has been discussed.

Keywords: EB virus; Graves’ disease; autoimmune polyglandular syndrome; type 1 diabetes mellitus.

MeSH terms

  • Biomarkers
  • Child
  • Epstein-Barr Virus Infections / complications*
  • Epstein-Barr Virus Infections / immunology*
  • Female
  • Glycated Hemoglobin
  • Humans
  • Immunoglobulin M
  • Lymphocyte Count
  • Polyendocrinopathies, Autoimmune / diagnosis
  • Polyendocrinopathies, Autoimmune / etiology*
  • Polyendocrinopathies, Autoimmune / immunology*
  • Thyrotropin / blood

Substances

  • Biomarkers
  • Glycated Hemoglobin A
  • Immunoglobulin M
  • hemoglobin A1c protein, human
  • Thyrotropin