Differentiating and Treating Stevens-Johnson Syndrome versus Contact Dermatitis
Stevens-Johnson Syndrome (SJS) requires immediate hospitalization and discontinuation of suspected causative agents, while contact dermatitis can typically be managed with topical steroids and allergen avoidance.
Key Differentiating Features
Clinical Presentation
| Feature | Stevens-Johnson Syndrome | Contact Dermatitis |
|---|---|---|
| Onset | Rapid, often with prodromal symptoms (fever, malaise) | Develops 24-96 hours after exposure |
| Distribution | Widespread, symmetrical | Localized to areas of contact |
| Mucosal Involvement | Prominent involvement of ≥2 mucosal surfaces (oral, ocular, genital) | Typically absent or limited |
| Skin Appearance | Blistering, epidermal detachment, Nikolsky sign positive | Erythema, vesicles, poorly defined borders |
| Pain | Severe cutaneous pain | Pruritus predominates |
| Systemic Symptoms | Fever, malaise, respiratory symptoms | Usually absent |
High-Risk Features Requiring Urgent Action
Immediate hospitalization is necessary if any of these are present 1:
- Mucosal involvement in ≥2 sites
- Skin detachment >10% body surface area
- Vesicles, skin/mucous detachment, pustules, purpura
- Nikolsky sign (skin sloughing with lateral pressure)
- Severe pain rather than itching
- Systemic symptoms (fever, malaise)
Diagnostic Approach
Skin Biopsy: Essential for definitive diagnosis of SJS, showing full-thickness epidermal necrosis with extensive keratinocyte apoptosis 2
Laboratory Testing:
- Complete blood count
- Liver and kidney function tests
- Consider bacterial cultures if infection suspected
Medication Review:
- High-risk medications for SJS include: allopurinol, sulfonamides, aminopenicillins, cephalosporins, carbamazepine, phenytoin, NSAIDs 2
Treatment Algorithm
If SJS is Suspected:
Immediate Actions:
Supportive Care (cornerstone of management):
- Fluid resuscitation
- Temperature regulation
- Pain management
- Wound care
- Nutritional support
- Prevention of secondary infections 1
Specific Interventions:
If Contact Dermatitis is Suspected:
Mild to Moderate (Grade 1-2):
- Identify and remove the allergen
- Topical corticosteroids appropriate for affected area (avoid high-potency steroids on face, groin, axillae) 4
- Oral antihistamines for pruritus
- Cool compresses
Severe (Grade 3):
- Short course of systemic corticosteroids (prednisone) 5
- Dermatology consultation
- Consider patch testing after resolution to identify specific allergen
Pitfalls and Caveats
Delayed Diagnosis: SJS can be mistaken for other conditions initially, delaying critical intervention. When in doubt, consult dermatology urgently.
Inappropriate Steroid Use: Starting treatment with steroids prior to ophthalmologic examination in cases with eye involvement may worsen conditions due to infection or mask accurate diagnosis 1.
Incomplete Medication Discontinuation: Failure to immediately stop all potential causative medications can lead to disease progression in SJS.
Misdiagnosis: Other conditions that can mimic SJS include:
- Staphylococcal scalded skin syndrome
- Erythema multiforme
- Bullous pemphigoid
- Drug-induced linear IgA dermatosis 2
Underestimating Severity: What appears initially as contact dermatitis may evolve into SJS. Progressive symptoms warrant reassessment.
Remember that SJS is a medical emergency with mortality rates of 1-5%, while TEN (the more severe form with >30% skin detachment) has mortality rates of 25-35% 2. Early recognition and appropriate management are critical for improving outcomes.