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临床少见的Stevens-Johson综合征一例并相关文献复习 被引量:2

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摘要 Stevens-Johson综合征(SJS)最早于1922年报道,又称渗出性多形红斑,是涉及皮肤、黏膜的全身综合征,病因较复杂,可由感染、药物及其他因素引起。本病发病急骤,患者多伴有发热、头痛、全身不适、关节痛、咽痛等较重的前驱症状,早期明确诊断较困难。我院近期收治1例,病初误诊,现结合相关文献分析报告如下。
出处 《临床误诊误治》 2014年第6期11-13,共3页 Clinical Misdiagnosis & Mistherapy
基金 解放军总医院科技创新苗圃基金(11KMZ04)
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  • 1Gerull R, Nelle M, Schaible T. Toxic epidermal necroly- sis and Stevens-Johnson syndrome: a review [ J ]. Crit Care Med, 2011,39(6) :1521-1532.
  • 2Auquier-Dunant A, Mockenhaupt M, Naldi L, et al. Cor- relations between clinical patterns and causes of erythema multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis: results of an international prospec- tive study[ J ]. Arch Dermatol, 2002,138 ( 8 ) : 1019-1024.
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