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Insights into Severe Cutaneous Adverse Drug Reactions: A 5-Year Retrospective Analysis of Stevens- Johnson Syndrome- Toxic Epidermal Necrolysis and Drug Rash with Eosinophilia and Systemic Symptoms. [PDF]
Indian Dermatol Online JKumaran MS +5 more
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Ofloxacin, paracetamol and cefixime induced Stevens-Johnson syndrome - toxic epidermal necrolysis in an adult female patient: a case report. [PDF]
J Pharm Health Care SciDesai MR +3 more
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Systemic immunomodulating therapies for epidermal necrolysis (Stevens-Johnson syndrome/toxic epidermal necrolysis): A systematic review and meta-analysis. [PDF]
J Dtsch Dermatol GesHeuer R +3 more
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Archives of Dermatology, 1978
To the Editor.— With regards to the brief report, "Permanent Anonychia After Stevens-Johnson Syndrome," in the JulyArchives(113:970, 1977), the authors state that nothing has been written about nail changes in the Stevens-Johnson syndrome. This is not the case.
J J, Chanda, J P, Callen
+7 more sources
To the Editor.— With regards to the brief report, "Permanent Anonychia After Stevens-Johnson Syndrome," in the JulyArchives(113:970, 1977), the authors state that nothing has been written about nail changes in the Stevens-Johnson syndrome. This is not the case.
J J, Chanda, J P, Callen
+7 more sources
European Journal of Pediatrics, 2007
A 13-year-old boy was brought to the emergency department (ED) with a generalized itchy rash of 2 days' duration. For the past 3 days, he had dry, itchy eyes with a purulent discharge (Figure 1) and nonbilious emesis 2 or 3 times per day, with some blood streaks in the vomitus on the third day of illness.
M H, de Ru, R N, Sukhai
openaire +2 more sources
A 13-year-old boy was brought to the emergency department (ED) with a generalized itchy rash of 2 days' duration. For the past 3 days, he had dry, itchy eyes with a purulent discharge (Figure 1) and nonbilious emesis 2 or 3 times per day, with some blood streaks in the vomitus on the third day of illness.
M H, de Ru, R N, Sukhai
openaire +2 more sources
Internal and Emergency Medicine, 2018
Stevens–Johnson syndrome is a rare, yet life-threatening, delayed-type hypersensitivity reaction characterized by mucocutaneous epidermal necrolysis. Toxic epidermal necrolysis is a severe manifestation of Stevens–Johnson syndrome, defined as greater than 30% skin detachment.
Wesley D, Davis, Phillip A, Schafer
openaire +4 more sources
Stevens–Johnson syndrome is a rare, yet life-threatening, delayed-type hypersensitivity reaction characterized by mucocutaneous epidermal necrolysis. Toxic epidermal necrolysis is a severe manifestation of Stevens–Johnson syndrome, defined as greater than 30% skin detachment.
Wesley D, Davis, Phillip A, Schafer
openaire +4 more sources
Archives of Internal Medicine, 1959
This syndrome is characterized by a variation in skin reaction, involvement of the mucous membranes, severe ophthalmia, and a marked general reaction. Stevens and Johnson, in 1922,1described two cases of dramatic onset with fever, conjunctivitis, and a cutaneous eruption, which thereafter has been known as Stevens-Johnson syndrome, or erythema ...
E, WASSERMAN, W I, GLASS
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This syndrome is characterized by a variation in skin reaction, involvement of the mucous membranes, severe ophthalmia, and a marked general reaction. Stevens and Johnson, in 1922,1described two cases of dramatic onset with fever, conjunctivitis, and a cutaneous eruption, which thereafter has been known as Stevens-Johnson syndrome, or erythema ...
E, WASSERMAN, W I, GLASS
openaire +2 more sources