Stevens Johnson syndrome and toxic epidermal necrolysis
Last Updated: 2023-07-07
Author(s): Anzengruber F., Navarini A.
ICD11: EB13.2
Last Updated: 2023-07-07
Author(s): Anzengruber F., Navarini A.
ICD11: EB13.2
Stevens Johnson Syndrome, SJS, Toxic epidermal necrolysis, TEN, Lyell syndrome, Epidermolysis necroticans combustiformis, Epidermolysis acuta toxica.
Rare, serious, potentially lethal, mucocutaneous disease, which is usually triggered by the ingestion of drugs. There is detachment of the epidermis and the appearance of necrosis. Stevens Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) correspond to one clinical picture. In 100% there is cheilitis and stomatitis. What differs is the extensive spread to the rest of the skin
Subepidermal blister cleft, necrotic keratinocytes in the epidermis at the blister roof, otherwise unchanged str. corneum, ↑ eosinophils in the epidermis, spiny cells with ballooned degeneration. In the corium lymphohistiocytic infiltrate, mainly arranged perivascularly.
SCORTEN (severity of illness score for toxic epidermal necrolysis) according to Bastuji-Garin | ||
---|---|---|
Age | ≥ 40 years | 1 |
Existing neoplasia? | Yes | 1 |
Body surface affected | >10% | 1 |
Heart rate | ≥120/minute | 1 |
Serum urea | >10 mmol/L | 1 |
Serum glucose | >14 mmol/L | 1 |
Serum bicarbonate | >20 mmol/L | 1 |
Always:
For mild (<< 10%) or no mucosal involvement:
In case of mucous membrane involvement
Anal region
For medium and heavy shapes:
General measures
Systemic therapy