Steven Johnson Sendromu: Olgu Sunumu

Stevens-Johnson Sendromu, akut başlangıçlı, genellikle kendini sınırlayan, vezikülobüllöz, deri lezyonlarının yanı sıra en az iki mukozal alanın tutulduğu bir hastalıktır. Etyolojide özellikle ilaçlar, çeşitli enfeksiyon ajanlar, malignite, kollagen doku hastalıkları rol oynamaktadır. Stevens-Johnson Sendromu olguların % 3-18’inde ölüme yol açmaktadır. Spesifik tedavisi yoktur. Sebep olan ajandan uzaklaşılması ve destek tedavisi ilk olarak uygulanacak tedavi yöntemidir. immunsupresif ilaçlar, hemodiyaliz, plazmaferez, hiperbarik oksijen diger tedavi secenekleridir. Bu çalışmamızda üst solunum yolu enfeksiyonu nedeniyle ilaç kullanımını takiben Stevens-Johnson Sendromu gelişen olguya tedavi yaklaşımını tartışmayı amaçladık

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Stevens-Johnson Syndrome is an acute, usually self-limiting disease of the skin and mucous membranes. Vesiculobullous skin lesions with two or more mucosal area are usually affected in this disease. Especially drugs, various infectious agents, malignancy, collagen tissue diseases are common etiological factors of Stevens-Johnson Syndrome. Rate of the patients’ mortality with SJS is %3-%18. There is no specific treatment. Early withdrawal of implicated agent and supportive therapy as applied to the first treatment method. Corticosteroids, intravenous immunoglobulin (IVIG), immunosuppressive drugs, hemodialysis, plasmapheresis, hyperbaric oxygen is the other treatment options. In this study, we aimed to discuss the treatment approach of Stevens-Johnson Syndrome on a case that developed Stevens-Johnson Syndrome following to use of drug for upper respiratory tract infection
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