Case Reports in Ophthalmology (Aug 2019)

A Case of IgG4-Related Bilateral Palpebral Conjunctivitis

  • Toshiya Nagai,
  • Tatsuya Yunoki,
  • Atsushi Hayashi

DOI
https://doi.org/10.1159/000502411
Journal volume & issue
Vol. 10, no. 2
pp. 299 – 303

Abstract

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The most common sites of IgG4-related ocular disease are the lacrimal glands, infraorbital nerve, and extraocular muscles. Other ocular adnexal sites are relatively rare. We report a rare case of an 83-year-old man who developed palpebral conjunctivitis following bilateral hypertrophic ectropion of the eyelid. Tissue immunostaining revealed many IgG4-positive plasma cells (67 IgG4/74 IgG cells/high-power field). The serum IgG4 level was 76.9 mg/dL, which was within the normal range. The diagnosis was probable IgG4-related disease. The possibility of IgG4-related disease should be considered in a patient presenting with refractory conjunctivitis and hyperemia or hypertrophy of the lower eyelid.

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