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Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are now believed to be variants of the same condition, distinct from erythema multiforme. SJS/TEN is a rare, acute, serious, and potentially fatal skin reaction in which there are sheet-like skin and mucosal loss. Using current definitions, it is nearly always caused by.


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Stevens-Johnson syndrome/toxic epidermal necrolysis is a rare, acute, serious, and potentially fatal skin reaction in which there are sheet-like skin and mucosal loss accompanied by systemic symptoms.


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Treatment is most successful when Stevens-Johnson syndrome and toxic epidermal necrolysis are recognized early and treated in an inpatient dermatologic or intensive care unit setting; treatment in a burn unit Treatment Burns are injuries of skin or other tissue caused by thermal, radiation, chemical, or electrical contact. Burns are classified.


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Stevens-Johnson syndrome, also called SJS, is a rare but serious problem. Most often, it's a severe reaction to a medicine you've taken. It causes your skin to blister and peel off. It affects.


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Stevens-Johnson syndrome is a rare skin condition in which a dark, blistering rash forms on the skin. It affects 1-2 million people each year. The condition usually affects upper body areas, such as the upper chest. Over time, it spreads to the face, arms, and across the rest of the body. Eventually, the rashes on the skin detach from the.


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Stevens-Johnson syndrome (SJS) is a rare condition, but when it happens, it's a medical emergency.. Skin will start to regrow in 2 to 3 weeks but could take several months to fully return.


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Starting a healthy skincare regimen—in infancy. When Johnson & Johnson's Consumer Microbiome Research Program launched in 2009, company scientists began their research work by looking at the skin profiles of the Johnson's® brand's tiniest users—babies.. Since then, they have been studying the evolution of the skin microbiome through the different stages of life, as well as the role.


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Stevens-Johnson syndrome (SJS) is a rare, potentially fatal skin disease that causes flu-like symptoms and a blistering, painful skin rash that makes skin peel. It's most often caused by medications but may also be caused by infections. Treatment typically requires hospitalization, medication to treat infections and supportive care.


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If the underlying cause of Stevens-Johnson syndrome can be eliminated and the skin reaction stopped, new skin may begin to grow within several days. In severe cases, full recovery may take several months. Self care. If you have had Stevens-Johnson syndrome, be sure to: Know what caused your reaction.


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Stevens-Johnson Syndrome and toxic epidermal necrosis (SJS/TEN) are very serious skin peeling conditions that are caused by an allergic reaction to medications or an illness. Hospitalized treatment includes stopping the problem medication, replacing electrolytes, applying skin dressings, and providing pain medications and antibiotics.


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About half the cases of Stevens-Johnson syndrome and nearly all the cases of toxic epidermal necrolysis are caused by a reaction to a drug, most often sulfa and other antibiotics; antiseizure drugs, such as phenytoin and carbamazepine; and certain other drugs, such as piroxicam or allopurinol.Some cases are caused by a bacterial infection, vaccination, or graft-versus-host disease Graft-versus.