2014
DOI: 10.1111/vde.12142
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Erythema multiforme, Stevens–Johnson syndrome and toxic epidermal necrolysis: a comparative review

Abstract: (1) Histopathological lesions do not reliably differentiate EM, SJS and TEN. (2) A multicentre study to develop a consensus set of clinical criteria for EM and SJS/TEN in animals is overdue. (3) No adjunctive therapies, including intravenous immunoglobulin and ciclosporin, have met evidence-based standards.

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Cited by 62 publications
(169 citation statements)
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References 137 publications
(307 reference statements)
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“…The present case had only oral mucosal involvement. Although this is present in the majority of SJS cases, and has been reported as one of the criteria to diagnose SJS, mucosal involvement is no longer required to make the diagnosis of SJS (BastujiGarin et al 1993;Yager 2014). The dermatopathological changes reflected a cytotoxic lymphocyte response against altered keratinocytes, as can also be seen in EM.…”
Section: Questionsmentioning
confidence: 95%
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“…The present case had only oral mucosal involvement. Although this is present in the majority of SJS cases, and has been reported as one of the criteria to diagnose SJS, mucosal involvement is no longer required to make the diagnosis of SJS (BastujiGarin et al 1993;Yager 2014). The dermatopathological changes reflected a cytotoxic lymphocyte response against altered keratinocytes, as can also be seen in EM.…”
Section: Questionsmentioning
confidence: 95%
“…For many years, the position in human dermatology has been that EM, SJS and TEN occupy a spectrum, with EM at the milder end and TEN at the severe extremity. The current position, however, is that EM is a separate disease, mostly triggered by infection with herpes simplex virus (Yager 2014). In contrast, SJS and TEN represent a spectrum of largely drug-induced disease.…”
Section: Questionsmentioning
confidence: 99%
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