Abstract
Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) represent a spectrum of life-threatening mucocutaneous reactions. SJS/TEN usually induced by drugs, with the structure of the drug and genetic profile of the patient playing important roles in the development, recovery and prognosis of the reaction. While there are currently no internationally accepted management guidelines for SJS/TEN, early recognition and prompt treatment are essential to improve patient outcomes.
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The article was adapted from the American Journal of Clinical Dermatology 2015;16(6):475–93 [1] by salaried/contracted employees of Adis/Springer and was not supported by any external funding.
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Adis Medical Writers. Stevens–Johnson syndrome and toxic epidermal necrolysis: early recognition and prompt management may reduce mortality. Drugs Ther Perspect 32, 238–243 (2016). https://doi.org/10.1007/s40267-016-0294-5
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DOI: https://doi.org/10.1007/s40267-016-0294-5