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Stevens-Johnson Syndrome MeSH Descriptor Data 2025
Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis.
Entry Term(s)
Drug-Induced Stevens Johnson Syndrome
Drug-Induced Stevens-Johnson Syndrome
Epidermal Necrolysis, Toxic
Lyell's Syndrome
Mycoplasma-Induced Stevens Johnson Syndrome
Mycoplasma-Induced Stevens-Johnson Syndrome
Nonstaphylococcal Scalded Skin Syndrome
Scalded Skin Syndrome, Nonstaphylococcal
Stevens Johnson Syndrome Toxic Epidermal Necrolysis
Stevens Johnson Syndrome Toxic Epidermal Necrolysis Spectrum
Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis.
An exfoliative disease of skin seen primarily in adults and characterized by flaccid bullae and spreading erythema so that the skin has the appearance of being scalded. It results primarily from a toxic reaction to various drugs, but occasionally occurs as a result of infection, neoplastic conditions, or other exposure.