증례

베체트 병으로 오인된 스티븐스 존슨 증후군 1예

이정우1, 김승균1, 박찬흠1, 홍석민1,*
Jung Woo Lee1, Seung Kyun Kim1, Chan Hum Park1, Seok Min Hong1,*
Author Information & Copyright
1한림대학교 의과대학 이비인후-두경부외과학교실
1Department of Otorhinolaryngology-Head & Neck Surgery, College of Medicine Hallym University, Chuncheon, Korea
*교신저자: 홍석민, 200-704 강원도 춘천시 교동 153 한림대학교 의과대학 이 비 인후-두경 부외과학교실 전화:(033) 240-5181· 전송:(033) 241-2909 E-mail: thecell@medimail.co.kr

© Copyright 2012 The Busan, Ulsan, Gyeoungnam Branch of Korean Society of Otolaryngology-Head and Neck Surgery. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Nov 28, 2011; Revised: Feb 02, 2012; Accepted: Mar 02, 2012

Published Online: May 31, 2020

ABSTRACT

Stevens-Johnson syndrome (SJS) is a rare, but fatal and acute drug-induced cutaneous reaction which presents dramatic, unforgettable manifestations. Though the characteristic features of the disease are well known generally, many clinicians have not experienced a case of SJS frequently, which may result in delay in diagnosis and treatment of it. The authors report a rare case of SJS, which was initially misdiagnosed as Behcet’s disease, with literature review. (J Clinical Otolaryngol 2012;23:121–124)

Keywords: 스티븐스 존슨증후군; 베체트병
Keywords: Stevens-Johnson syndrome; Behcet’s disease