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Vulvovaginal Involvement in Pediatric Stevens-Johnson Syndrome: A Case Series
Max Holtz1, Frances Grimstad2, Jeannette Higgins3
1Childrens' Mercy Hospital and University of Missouri Kansas City, Kansas City, Missouri, and Department of Obstetrics and Gynecology, University of Missouri Kansas City, Kansas City, Missouri; Department of Women's Health, Dell Medical School, The University of Texas, Austin, Texas.
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe skin reactions. Vulvovaginal involvement can occur, but prompt management may prevent lasting damage.
Area of Science:
- Dermatology
- Toxicology
- Gynecology
Background:
- Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe, life-threatening mucocutaneous hypersensitivity reactions.
- These reactions are characterized by prodromal symptoms followed by widespread rash due to keratinocyte apoptosis and epidermal detachment.
Observation:
- Three adolescent patients presented with SJS/TEN involving the vulvovaginal area after starting lamotrigine, trimethoprim-sulfamethoxazole, and phenobarbital.
- Treatment included intravenous immunoglobulin, steroids, etanercept in one case, topical emollients, and meticulous perineal hygiene.
Findings:
- Vulvovaginal SJS/TEN can lead to permanent architectural changes if not managed promptly.
- Early interventions such as medication withdrawal, systemic corticosteroids, intravenous immunoglobulin, and supportive care are crucial.
- Vaginoscopy confirmed no permanent sequelae in one patient, highlighting the potential for full recovery.
Implications:
- Prompt diagnosis and management of vulvovaginal SJS/TEN are essential to prevent long-term complications.
- A multidisciplinary approach involving dermatology, gynecology, and supportive care is recommended.
- Further research into optimal management strategies for SJS/TEN with mucosal involvement is warranted.
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