Abstract

Volume.122 Number.9

Original article : Case report

A Case of Stevens-Johnson Syndrome Requiring Differentiation from Kawasaki Disease in the Acute Phase
Kaori Matsumoto1,2, Hideki Fukuoka1, Akimasa Tomida3, Risa Mineoka4, Tsutomu Inatomi1, Mayumi Ueta1, Chie Sotozono1
1 Department of Ophthalmology, Kyoto Prefectural University of Medicine
2 Baptist Eye Clinic
3 Department of Pediatrics, Kyoto Prefectural University of Medicine
4 Department of Dermatology, Kyoto Prefectural University of Medicine

Background: Stevens-Johnson syndrome (SJS) causes ocular disease in the acute stage and severe visual impairment in the late stage. Severe ocular findings during the acute phase are more likely to be noted when the age of onset is younger, making early, appropriate diagnosis important. Herein, we report the case of a patient who was initially diagnosed with Kawasaki disease by a pediatrician and was later correctly diagnosed with SJS by a dermatologist and an ophthalmologist.
Case report: The patient was an 8-year-old boy who initially presented at Clinic A due to a fever, sore throat, and conjunctival hyperemia in both eyes. Antihistamine agents, expectorants, bronchodilators, antiplasmin agents, and third-generation cephem antibiotics were administered because of presumed common cold-like symptoms. However, his sore throat worsened the following day, and a systemic rash developed over his entire body. He subsequently visited General Hospital B and was admitted with suspected Kawasaki disease. After admission, the on-duty ophthalmologist discovered that he was afflicted with bilateral pseudomembranous conjunctivitis, and he was then transferred to our hospital due to suspected SJS. He was finally diagnosed with SJS due to atypical target-shaped erythema, flare/swelling and erosion of oral/labial mucosa with blood crust and bleed, bilateral pseudomembranous conjunctivitis, and conjunctival epithelial defect. We successfully treated the patient with pulse steroid therapy and the topical administration of betamethasone eye drops, with no continued visual impairment.
Conclusion: Examination by both a dermatologist and an ophthalmologist is useful for the early diagnosis and treatment of SJS.
Nippon Ganka Gakkai Zasshi (J Jpn Ophthalmol Soc) 122: 705-710, 2018.

Key words
Stevens-Johnson syndrome (SJS), Toxic epidermal necrolysis (TEN), Kawasaki disease, Pediatrics, Epithelial defect
Reprint requests to
Kaori Matsumoto, M.D. Baptist Eye Clinic. 12 Kamiikeda-cho, Kitashirakawa, Sakyo-ku,, Kyoto 606-8287, Japan