Results 1 to 10 of about 104,558 (185)

Case Report: Hydronephrosis and nephrogenic adenoma secondary to Stevens-Johnson syndrome [PDF]

open access: yesFrontiers in Pharmacology
IntroductionStevens–Johnson syndrome is a rare, severe cutaneous adverse reaction. There is a lack of literature reporting the complications of the bladder and ureter caused by Stevens–Johnson syndrome.
Chuan Wang, Yidong Huang
doaj   +2 more sources

Co-amoxiclav-induced Stevens Johnson syndrome in a child [PDF]

open access: yesThe Pan African Medical Journal, 2013
Stevens-Johnson Syndrome is an uncommon life threatening disease generally induced by drugs. Antibiotics, mainly sulphonamides, are the most involved drugs in Stevens-Johnson Syndrome in children. Co-amoxiclav is a well tolerated antibiotic. It has never
Neila Fathallah   +6 more
doaj   +3 more sources

Stevens–Johnson syndrome/toxic epidermal necrolysis as the initial presentation of paraneoplastic anti-TIF1-γ dermatomyositis [PDF]

open access: yesSAGE Open Medical Case Reports
We report a rare case of Stevens–Johnson syndrome/toxic epidermal necrolysis as the initial manifestation of paraneoplastic dermatomyositis in a 50-year-old man subsequently diagnosed with diffuse large B cell lymphoma, in the absence of any identifiable
Ghassan Barnawi   +4 more
doaj   +2 more sources

Nevirapine-induced Stevens–Johnson Syndrome in an HIV-exposed neonate: A case report [PDF]

open access: yesIDCases
A term male infant developed a blistering muco-cutaneous rash in the second week of life following postnatal HIV prophylaxis with nevirapine (NVP). Clinical findings were consistent with Stevens-Johnson syndrome. Following NVP discontinuation, the infant
Eimear M. O’Connell   +3 more
doaj   +2 more sources

Evaluation of conjunctival bacterial flora in patients with Stevens-Johnson Syndrome [PDF]

open access: yesClinics, 2014
OBJECTIVE: To determine the conjunctival bacterial flora present in patients with Stevens-Johnson syndrome. METHODS: A prospective study of the conjunctival bacterial flora was performed in 41 eyes of 22 patients with Stevens-Johnson syndrome.
Luciana Frizon   +6 more
doaj   +5 more sources

Stevens-Johnson Syndrome – clinical symptoms, etiology, pathophysiology and medical treatment - a review of the literature [PDF]

open access: yesJournal of Education, Health and Sport, 2022
Stevens-Johnson syndrome (SJS) is a rare disease of the skin and mucous membrane. It develops as a result of a sudden skin reaction, which is most often triggered by the use of certain drugs. It is characterized by acute epidermal necrosis.
Karolina Szymkiewicz   +3 more
doaj   +3 more sources

Mycoplasma-pneumonia-induced Stevens–Johnson syndrome in an adult: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Stevens–Johnson syndrome epitomizes an acute, exceptionally rare, and capricious immunological phenomenon marked by potentially life-threatening skin reactions, involvement of mucous membranes, and concomitant systemic manifestations.
Fathima Thesleem Yoosuf   +6 more
doaj   +2 more sources

Bronchiolitis obliterans associated with toxic epidermal necrolysis induced by infection: A case report and literature review

open access: yesFrontiers in Pediatrics, 2023
BackgroundStevens-Johnson syndrome/toxic epidermal necrolysis has a severe impact on patients' eyes, genital mucosa, and many other organs. Bronchiolitis obliterans is a rare complication of Stevens-Johnson syndrome/toxic epidermal necrolysis.Data ...
Jingwei Liu   +3 more
doaj   +1 more source

Daunorubicin induced Stevens‐Johnson syndrome: A case report

open access: yesClinical Case Reports, 2021
Clinicians should consider the possible association of Daunorubicin with Stevens‐Johnson syndrome (SJS), administer it with caution and promptly evaluate all subsequently developing cutaneous reactions with a high index of suspicion for Stevens‐Johnson ...
Preeti Shakya, Amit Sharma Nepal
doaj   +1 more source

Case report: Development of vanishing bile duct syndrome in Stevens-Johnson syndrome complicated by hemophagocytic lymphohistiocytosis

open access: yesFrontiers in Medicine, 2022
BackgroundVanishing bile duct syndrome is a rare drug-induced disease characterized by cholestasis and ensuing ductopenia. Dermatological manifestations of drug hypersensitivity such as Stevens-Johnson syndrome and toxic epidermal necrolysis may also ...
Wan-Chen Lin   +5 more
doaj   +1 more source

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