Nihon Hifu Meneki Arerugy Gakkai Zasshi
Online ISSN : 2433-7854
Print ISSN : 2433-7846
Review
Genetic Predisposition and Pathogenesis of Stevens-Johnson syndrome/Toxic Epidermal Necrolysis with Severe Ocular complications
Genetic Predisposition and Pathogenesis of SJS/TEN
Mayumi UETA
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2020 Volume 3 Issue 2 Pages 282-293

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Abstract

 Stevens-Johnson syndrome(SJS)is an acute inflammatory vesiculobullous reaction of the skin and mucosa such as the ocular surface, oral cavity, and genitals. In patients with extensive skin detachment and a poor prognosis, the condition is called toxic epidermal necrolysis(TEN). Severe ocular complications(SOC)appear in about half of SJS/TEN patients diagnosed by dermatologists. Ophthalmologists tend to report both SJS and TEN with severe ocular complications as“SJS”in a broad sense. Cold medicines, including multi-ingredient cold medications and non-steroid anti-inflammatory drugs(NSAIDs)were the main causative drugs of SJS/TEN with SOC in all SJS and TEN patients.

 Cold medicine-related SJS/TEN(CM-SJS/TEN)with SOC was strongly associated with HLA-A02 : 06 in the Japanese populations, and significantly associated with some genes such as IKZF1 gene. As we found several HLA-SNP sets with a high odds ratio, we postulated that they may help to predict the possible development of SJS/TEN with SOC.

(日本皮膚免疫アレルギー学会雑誌, 3(2):282-293, 2020)

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© 2020 The Japanese Society for Cutaneous Immunology and Allergy
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