Results 271 to 280 of about 197,989 (298)
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New England Journal of Medicine, 2005
A 22-year-old woman with a history of a seizure disorder presented to the emergency department after having a rash for three days and a fever for one day. The rash began as a maculopapular distribution on the neck and chest and rapidly progressed to target lesions and bullae (Panels A and B) that involved all surfaces of the integument and spared only ...
Jordan D. Fein, Kendal L. Hamann
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A 22-year-old woman with a history of a seizure disorder presented to the emergency department after having a rash for three days and a fever for one day. The rash began as a maculopapular distribution on the neck and chest and rapidly progressed to target lesions and bullae (Panels A and B) that involved all surfaces of the integument and spared only ...
Jordan D. Fein, Kendal L. Hamann
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International Journal of Dermatology, 1985
ABSTRACT: Stevens‐Johnson syndrome is relatively rare. The authors report a retrospective study of 34 patients seen at the University Hospital in Malaysia over 16 years and discuss the epidemiology, clinical features, complications, investigations, etiologic association, mortality, sequelae, course of the disease, and the use of steroid.
B. A. Adam, H. C. Ting
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ABSTRACT: Stevens‐Johnson syndrome is relatively rare. The authors report a retrospective study of 34 patients seen at the University Hospital in Malaysia over 16 years and discuss the epidemiology, clinical features, complications, investigations, etiologic association, mortality, sequelae, course of the disease, and the use of steroid.
B. A. Adam, H. C. Ting
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Stevens–Johnson syndrome in children
Current Opinion in Pediatrics, 2022Purpose of review The concept of Stevens–Johnson syndrome (SJS) in children is evolving. This manuscript reviews recent advances with the lens of new terminology namely infection-triggered reactive infectious mucocutaneous eruption and drug-induced epidermal necrolysis, with the objective of integrating this novel terminology ...
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Detector: Jurnal Inovasi Riset Ilmu Kesehatan
Stevens-Johnson Syndrome (SJS) is an antibody-mediated disease characterized by prodromal symptoms followed by severe mucocutaneous manifestations. The more severe form of SJS is Toxic Epidermal Necrolysis (TEN), which causes an inflammatory response ...
Dhannisa +4 more
semanticscholar +1 more source
Stevens-Johnson Syndrome (SJS) is an antibody-mediated disease characterized by prodromal symptoms followed by severe mucocutaneous manifestations. The more severe form of SJS is Toxic Epidermal Necrolysis (TEN), which causes an inflammatory response ...
Dhannisa +4 more
semanticscholar +1 more source
Late-onset Stevens–Johnson syndrome due to nivolumab use for hepatocellular carcinoma
Journal of Oncology Pharmacy Practice, 2019Nivolumab is a fully human immunoglobulin G4 immune checkpoint inhibitor antibody approved for use in the treatment of several malignancies. Severe side effects such as Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) have only extremely ...
C. Dasanu
semanticscholar +1 more source
Journal of the European Academy of Dermatology and Venereology, 2019
The SCORTEN score is a specific predictor of the probability of death for patients diagnosed with Stevens‐Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN).
I. Torres-Navarro +3 more
semanticscholar +1 more source
The SCORTEN score is a specific predictor of the probability of death for patients diagnosed with Stevens‐Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN).
I. Torres-Navarro +3 more
semanticscholar +1 more source
Conjunctival Pigmentation in Stevens-Johnson Syndrome
Annals of Ophthalmology, 2007We report a 29-year-old white woman with conjunctival pigmentation after a Stevens-Johnson syndrome (SJS) episode triggered by sulfasalazine. The patient developed bilateral tarsal and forniceal conjunctiva and black pigmentation. Diagnostic biopsy showed stromal monocyte infiltration consistent with chronic phase SJS and conjunctival pigment of ...
MC Méndez +5 more
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Management of Stevens-Johnson Syndrome-Toxic Epidermal Necrolysis: Looking Beyond Guidelines!
Indian Journal of Dermatology, 2018Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe cutaneous adverse reactions, which are mainly caused by drugs; and these are usually associated with high degree of morbidity and mortality.
R. Kumar, Anupam Das, S. Das
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Stevens-Johnson syndrome in children
The Pediatric Infectious Disease Journal, 1982During a 22-year period 51 cases of Stevens-Johnson syndrome (SJS) occurred in infants and children who ranged in age from 3 months to 14 years. Fifty-six percent of patients had an antecedent upper respiratory tract infection or non-specific viral infection, and 67% had received a prescription medication in the 3 weeks before onset of SJS.
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Current Perspectives on Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
Clinical reviews in allergy and immunology, 2018M. Lerch +3 more
semanticscholar +1 more source