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Stevens-Johnson Syndrome, Pediatric Updated 4/2010

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BASICS

  • Description
  • Epidemiology
  • Pathophysiology
  • Etiology

DIAGNOSIS

  • Signs and Symptoms
  • Tests
  • Differential Diagnosis

TREATMENT

  • Initial Stabilization
  • General Measures
  • Medication (Drugs)

Ongoing Care

  • Prognosis
  • Complications
  • Patient Monitoring
The following is an excerpt....
BASICS
Description
  • Stevens-Johnson Syndrome (SJS) is a severe hypersensitivity reaction, characterized by diffuse bullous lesions, mucocutaneous involvement, and marked constitutional symptoms.
  • SJS is often considered to lie on a spectrum between erythema multiforme minor (EM minor) on 1 extreme, and toxic epidermal necrolysis (TEN) on the other, but this classification is controversial. In this schema, SJS is defined as involving >2 mucous membranes and <10% of total body surface area, and TEN as involving >30%, with overlap in between.
Epidemiology

Affects all ages, ethnicities, and both genders equally

Incidence

Incidence is 2–3 cases per million people each year.

Pathophysiology
  • SJS is an acute hypersensitivity reaction, characterized by a cell-mediated immunologic reaction.
  • A prodrome of 1–14 days is often seen, consisting of constitutional symptoms, including high fever ...

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See Also
Images >
1.70. One month after the acute onset of Stevens-Johnson syndrome, there is still active conjunctival and corneal inflammation and already significant symblepharon formation.Credit: From Tasman W, Jaeger E. The Wills Eye Hospital Atlas of Clinical Ophthalmology, 2e. Lippincott Williams & Wilkins, 2001
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