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Vulvovaginal and ocular involvement and treatment in female patients with Stevens–Johnson syndrome and toxic epidermal necrolysis: A review

  • M. Teresa Magone*
  • , Mary Maiberger
  • , Janine Clayton
  • , Helena Pasieka
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

3 Scopus citations

Abstract

Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are serious adverse cutaneous drug reactions, characterized by epidermal detachment and mucous membrane involvement. SJS/TEN is more common in female patients, with unique findings in the ocular and vulvar regions. Early recognition and intervention, as well as long-term follow-up, are crucial to prevent devastating scarring and sequelae. This review examines the vulvar and ocular manifestations of SJS/TEN and describes the current treatment recommendations for female patients, requiring close consultation and collaboration among dermatology, ophthalmology, and gynecology.

Original languageEnglish
Pages (from-to)520-528
Number of pages9
JournalInternational Journal of Women's Dermatology
Volume7
Issue number5
DOIs
StatePublished - Dec 2021

Keywords

  • Stevens–Johnson syndrome
  • cutaneous drug eruption
  • dry eye
  • ocular-surface
  • toxic epidermal necrolysis
  • vulvar involvement

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