Stevens-Johnson syndrome: Difference between revisions

From IDWiki
Content deleted Content added
No edit summary
 
Line 25: Line 25:
* Onset typically 1 to 3 weeks, but ranges from a few days up to 8 weeks
* Onset typically 1 to 3 weeks, but ranges from a few days up to 8 weeks
* Characterized by large blisters, large areas of skin detachment, confluent areas of erythema, atypical target lesions, purpura
* Characterized by large blisters, large areas of skin detachment, confluent areas of erythema, atypical target lesions, purpura
* Nikolsky sign
* [[Nikolsky sign]]
* Classified as SJS if less than 10% body surface area involved, or TEN if ≥30%
* Classified as SJS if less than 10% body surface area involved, or TEN if ≥30%
* May have fever or influenza-like illness
* May have fever or influenza-like illness
* May have respiratory symptoms
* May have respiratory symptoms
* May have lymphopenia and AKI
* May have lymphopenia and AKI

=== Prognosis ===

* Mortality is 10 to 40%, depending on severity
* Can develop superimposed bacterial infections
* After withdrawal of the offending drug, re-epithelialization starts around 1 week and lasts up to 3 weeks
* Can result in permanent scarring, hyperpigmentation, alopecia, nail loss, vision loss, synechiae, dry eye, dental problems

== Differential Diagnosis ==

* [[Erythema multiforme]]
* [[Coxsackievirus]]
* [[Mycoplasma pneumoniae]]
* Linear IgA bullous dermatosis
* Generalized bullous fixed-drug eruption
* Methotrexate toxicity
* [[Graft-versus-hosts disease]]
* [[Staphylococcal scalded skin syndrome]]
* [[Systemic lupus erythematosus]]
* [[Pemphigus vulgaris]]


== Diagnosis ==
== Diagnosis ==

* Diagnosis is based on histopathology of a skin biopsy, which will show full-thickness epidermal necrosis, focal adnexal necrosis, necrotic keratinocytes, and mild mononuclear cell dermal infiltrate
** Negative direct immunofluorescence tests


== Management ==
== Management ==

Latest revision as of 00:35, 7 January 2026

Background

Etiology

Clinical Manifestations

  • Onset typically 1 to 3 weeks, but ranges from a few days up to 8 weeks
  • Characterized by large blisters, large areas of skin detachment, confluent areas of erythema, atypical target lesions, purpura
  • Nikolsky sign
  • Classified as SJS if less than 10% body surface area involved, or TEN if ≥30%
  • May have fever or influenza-like illness
  • May have respiratory symptoms
  • May have lymphopenia and AKI

Prognosis

  • Mortality is 10 to 40%, depending on severity
  • Can develop superimposed bacterial infections
  • After withdrawal of the offending drug, re-epithelialization starts around 1 week and lasts up to 3 weeks
  • Can result in permanent scarring, hyperpigmentation, alopecia, nail loss, vision loss, synechiae, dry eye, dental problems

Differential Diagnosis

Diagnosis

  • Diagnosis is based on histopathology of a skin biopsy, which will show full-thickness epidermal necrosis, focal adnexal necrosis, necrotic keratinocytes, and mild mononuclear cell dermal infiltrate
    • Negative direct immunofluorescence tests

Management

  • Risk stratify with SCORTEN score
  • Consider referral to burn centre or ICU if BSA 30% or greater, or if SCORTEN score is 2 or greater
  • Stop offending drug, if applicable
  • Supportive care, including wound care and IV fluids (2 ml per kg times BSA over first 24 hours)
    • Room temperature 30º to 32ºC
    • May need NG tube
    • Pain control, as pain may be severe
  • Ophthalmologic exam and management
    • Saline rinses
    • Artificial tears even if no involvement
    • Corticosteroids with or without antibiotics for any involvement
  • No clear benefit to steroids or IVIG
  • Cyclosporine 3 to 5 mg per kg in one or two divided doses may slow progression

References

  1. ^  SK Tan, YK Tay. Profile and Pattern of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in a General Hospital in Singapore: Treatment Outcomes. Acta Dermato Venereologica. 2012;92(1):62-66. doi:10.2340/00015555-1169.