Stevens-Johnson syndrome: Difference between revisions
From IDWiki
Content deleted Content added
Created page with " == Etiology == * Infection: especially common in children ** Mycoplasma pneumoniae: moderate to severe involvement of two or more mucosal sites and sparse, or even absent..." |
No edit summary |
||
| (7 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
== Background == |
|||
* A [[severe cutaneous adverse reaction]] |
|||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
** Allopurinol |
|||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
** |
**[[Allopurinol]] |
||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
| ⚫ | |||
** |
**[[Nevirapine]] |
||
| ⚫ | |||
*** [[Amoxicillin]]/[[ampicillin]] |
|||
| ⚫ | |||
| ⚫ | |||
*** |
***[[Doxycycline]] |
||
*** |
***[[Amoxicillin]]/[[ampicillin]] |
||
| ⚫ | |||
***[[Levofloxacin]] |
|||
***[[Rifampin]] |
|||
== 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 == |
|||
* [[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 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 |
|||
Latest revision as of 00:35, 7 January 2026
Background
Etiology
- Infection: especially common in children
- Mycoplasma pneumoniae: moderate to severe involvement of two or more mucosal sites and sparse, or even absent, skin involvement
- Neisseria gonorrhoeae1
- Drugs
- Allopurinol
- Aromatic antiepileptic drugs and lamotrigine
- Antibacterial sulfonamides (including sulfamethoxazole and sulfasalazine)
- Nevirapine
- Oxicam nonsteroidal anti-inflammatory drugs (NSAIDs)
- Less strongly, other antibiotics
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
- 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 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
- ^ 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.