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Conjunctiva

Stevens-Johnson Syndrome (Ocular Sequelae)

Also known as: SJS, Stevens Johnson, toxic epidermal necrolysis, ocular sequelae SJS, symblepharon, cicatrising conjunctivitis

Filed as: Urgent

Source-cited from the record's own evidence list. Clinical content programme led by Dr Ankit Mathur, PhD, Grad Cert Ocu Thera, B.S. Optom. How the clinical content is governed

Overview

Ocular sequelae of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). Systemic mucocutaneous disease with acute and chronic ocular involvement. Chronic complications include symblepharon, dry eye, lid malposition, trichiasis, limbal stem cell deficiency, and corneal vascularisation. Long-term management: control inflammation, treat dry eye, manage trichiasis and lid pathology. Be cautious when changing or introducing new medications — can trigger severe exacerbation.

Recognition

Symptoms: what patients report

  • Very dry and sore eyes despite lubricants.
  • Blurred vision.
  • Recurrent episodes of swelling, redness, irritation.
  • Trichiasis — lashes touching globe.

Signs: what the examination shows

  • Symblepharon — fusion of bulbar and forniceal conjunctiva.
  • Vascularised corneal pannus.
  • Punctate epithelial erosions, particularly inferior.
  • Low Schirmer values (e.g. 2–4 mm in 5 minutes).
  • Trichiasis, lid margin keratinisation, entropion.
  • Chronic conjunctivitis with minimal discharge.

What OptoGuide™ covers for stevens-johnson syndrome (ocular sequelae)

  • Pattern reasoning: what this combination of findings points to, and its differentiators
  • Don't-miss risks and escalation triggers
  • Management tiers with linked Australian therapeutics
  • Referral urgency, specialty, and letter drafting

Sources

Standard texts: Kanski's Clinical Ophthalmology: A Systematic Approach, The Wills Eye Manual, Oxford Handbook of Ophthalmology, Oxford American Handbook of Ophthalmology, Signs in Ophthalmology: Causes & Differential Diagnosis.

Full bibliography

Other conjunctiva conditions

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