Stevens-Johnson syndrome: Pathogenesis, diagnosis, and management

被引:73
作者
Hazin, Ribhi [4 ]
Ibrahimi, Omar A. [3 ]
Hazin, Moustafa I. [2 ]
Kimyai-Asadi, Arash [1 ]
机构
[1] DermSurg Assoc, Houston, TX 77030 USA
[2] St Josephs Hosp, Dept Internal Med, Phoenix, AZ USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Dermatol, Boston, MA USA
[4] Harvard Univ, Fac Arts & Sci, Cambridge, MA 02138 USA
关键词
Stevens-Johnson syndrome; toxic epidermal necrolysis; erythema multiforme; intravenous immunoglobulins; adverse drug reaction; drug hypersensitivity; dermatological emergencies; mucocutaneous lesions; HLA B1501/HLA B1502; keratinocyte apoptosis;
D O I
10.1080/07853890701753664
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cutaneous drug reactions are the most common type of adverse drug reaction. These reactions, ranging from simple pruritic eruptions to potentially life-threatening events, are a significant cause of iatrogenic morbidity and mortality. Stevens-Johnson syndrome (SJS) is a serious and potentially life-threatening cutaneous drug reaction. Although progress has been made in the management of SJS through early detection, prompt hospitalization, and immediate cessation of offending agents, the prevalence of permanent disabilities associated with SJS remains unchanged. Nevertheless, despite being a problem that is global in scope, government and health care agencies worldwide have yet to find a consensus on either diagnostic criteria or therapy for this disorder. Here, we provide the internist and emergency room physician with a brief review the SJS literature and summarize the latest recommended interventions with the hope of improving early recognition of this disease and prevention of permanent sequelae and mortality that frequently complicate SJS.
引用
收藏
页码:129 / 138
页数:10
相关论文
共 135 条
[1]   HLA-B locus in Caucasian patients with carbamazepine hypersensitivity [J].
Alfirevic, Ana ;
Jorgensen, Andrea L. ;
Williamson, Paula R. ;
Chadwick, David W. ;
Park, B. Kevin ;
Pirmohamed, Munir .
PHARMACOGENOMICS, 2006, 7 (06) :813-818
[2]   Numerical, morphological and phenotypic changes in Langerhans cells in the course of murine graft-versus-host disease [J].
Asagoe, K ;
Takahashi, K ;
Yoshino, T ;
Kondo, E ;
Tanaka, R ;
Arata, J ;
Akagi, T .
BRITISH JOURNAL OF DERMATOLOGY, 2001, 145 (06) :918-927
[3]   Oral manifestations of erythema multiforme [J].
Ayangco, L ;
Rogers, RS .
DERMATOLOGIC CLINICS, 2003, 21 (01) :195-+
[4]   Differential diagnosis of severe cutaneous drug eruptions [J].
Bachot, N ;
Roujeau, JC .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2003, 4 (08) :561-572
[5]   SCORTEN: A severity-of-illness score for toxic epidermal necrolysis [J].
Bastuji-Garin, S ;
Fouchard, N ;
Bertocchi, M ;
Roujeau, JC ;
Revuz, J ;
Wolkenstein, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (02) :149-153
[6]   CLINICAL CLASSIFICATION OF CASES OF TOXIC EPIDERMAL NECROLYSIS, STEVENS-JOHNSON SYNDROME, AND ERYTHEMA MULTIFORME [J].
BASTUJIGARIN, S ;
RZANY, B ;
STERN, RS ;
SHEAR, NH ;
NALDI, L ;
ROUJEAU, JC .
ARCHIVES OF DERMATOLOGY, 1993, 129 (01) :92-96
[7]   Toxic epidermal necrolysis [J].
Becker, DS .
LANCET, 1998, 351 (9113) :1417-1420
[8]   Increased incidence of Lyme borreliosis in southern Sweden following mild winters and during warm, humid summers [J].
Bennet, L. ;
Halling, A. ;
Berglund, J. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2006, 25 (07) :426-432
[9]   Photo-induced Stevens-Johnson syndrome due to sulfasalazine therapy [J].
Borrás-Blasco, J ;
Navarro-Ruiz, A ;
Matarredona, J ;
Devesa, P ;
Montesinos-Ros, A ;
González-Delgado, M .
ANNALS OF PHARMACOTHERAPY, 2003, 37 (09) :1241-1243
[10]  
Cac NN, 2007, CUTIS, V79, P119