A Case of Stevens-Johnson Syndrome with Vanishing Bile Duct Syndrome
- Author:
Ji Hae AN
1
;
Seon Gu LEE
;
Dong Hyun KIM
;
Moon Soo YOON
;
Hee Jung LEE
Author Information
1. Department of Dermatology, CHA Bundang Medical Center, CHA University, Seongnam, Korea. derma97@gmail.com
- Publication Type:Case Report
- Keywords:
Stevens-Johnson syndrome;
Vanishing bile duct syndrome
- MeSH:
Bile Ducts;
Bile;
Cholestasis;
Drug Hypersensitivity;
Humans;
Korea;
Stevens-Johnson Syndrome
- From:Korean Journal of Dermatology
2019;57(5):258-261
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Stevens-Johnson syndrome (SJS) is a serious and potentially life-threatening disease. Vanishing bile duct syndrome (VBDS) is a rare cause of progressive cholestasis. Both syndromes are usually associated with the use of specific drugs. VBDS in patients with SJS is most commonly associated with drug hypersensitivity. To our knowledge, to date, the literature contains only a single report of toxic epidermal necrolysis associated with VBDS in Korea. We report a case of drug-induced SJS with acute onset of VBDS and present a review of the literature in this context. This case highlights the importance of awareness among clinicians regarding drug reactions, their severity, as well as diagnostic modalities and optimal management strategies in these cases.
