Wiley Acta Medica Okayama 2050-0904 12 3 2024 Vogt-Koyanagi-Harada disease in pregnancy: Case report and review of 32 patients in the literature e8643 EN Toshihiko Matsuo Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University Kasumi Takahashi Division of Obstetrics and Gynecology, Ochiai Hospital Tsunemasa Kondo Division of Obstetrics and Gynecology, Ochiai Hospital A 30-year-old woman in 31 weeks of pregnancy with metamorphopsia and headache was diagnosed Vogt-Koyanagi-Harada disease. She underwent steroid pulse therapy and oral prednisolone 20 mg daily for 3 weeks until complete resolution of serous retinal detachment monitored by optical coherence tomography. Oral prednisolone was tapered and discontinued until uneventful delivery. No potential conflict of interest relevant to this article was reported.