Toxic Epidermal Necrolysis
Basics
Basics
Basics
Description
Description
- One of the most fulminant and potentially fatal of all mucocutaneous disorders
- Skin sloughing at the dermal–epidermal interface results in the equivalent of a second-degree burn
- Can affect up to 100% of total body surface area (BSA)
- May extend to involve:
- GI mucosa
- Respiratory mucosa
- Genitourinary/renal epithelium
- Mechanism believed to be linked to T-cell–mediated cytotoxicity
- A delayed type hypersensitivity reaction triggered by specific drugs, infections, or idiopathic triggers
- Genetic susceptibility also appears to play a role
- Toxic epidermal necrolysis (TEN) is included in a disease continuum with Stevens–Johnson syndrome (SJS). Current classification system includes 3 categories based on percentage of total BSA:
- SJS: <10% of BSA
- SJS–TEN overlap syndrome: 10–30% of BSA
- TEN: >30% of BSA, can affect up to 100% BSA
- Risk factors:
- Age 1–10
- Age >70
- HIV
- Active malignancy particularly hematologic
- Liver and kidney disease
- Genetic factors have been identified such as certain HLA types
- Mortality rate overall ranges from 10% for SJS to up to 34% for TEN, usually due to secondary sepsis, acute respiratory distress syndrome (ARDS), and multisystem organ failure
- Synonym(s):
- Lyell syndrome
- Epidermolysis necroticans combustiformis
Pediatric Considerations
- A recent study found lower mortality rates in children: 0% SJS, 4% SJS/TEN, and 16% TEN
- Predictors of mortality in children include: Renal failure, sepsis, epilepsy, any bacterial infection and malignancy
Etiology
Etiology
- Dose-independent drug reactions are the usual cause of TEN:
- Onset time varies, most commonly 4–28 d from initiation of medication, but may be delayed up to 30 wk
- Frequently implicated drugs include:
- Sulfonamide and PCN antibiotics
- Anticonvulsants (carbamazepine, phenytoin, phenobarbital, lamotrigine)
- NSAIDs (oxicams, pyrazoles, sulindac)
- Allopurinol
- Corticosteroids
- Antiretroviral drugs
- Herbal remedies
- New biologic agents
- Other rare causes: Infections, specifically Mycoplasma pneumoniae in children, graft-versus-host disease, vaccinations, idiopathic cases (combined <4%)
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