Abstract
AmacHenoch Schonlein purpurasi (HSP) tanili hastalarin klinik ve laboratuvar karakteristiklerinin degerlendirilmesi, prognozu etkileyen risk faktorlerinin literatur esliginde incelenmesi.Gerec ve yontemAbant Izzet Baysal Universitesi Tip Fakultesi Cocuk Sagligi ve Hastaliklari Anabilim Dali'nda izlenen HSP tanili hastalarin tibbi kayitlari geriye donuk olarak incelendi. Bulgular Hasta populasyonu 46 cocuktan olusmaktadir (25 erkek, 21 kiz, ortalama yas: 6,4, yas araligi: 3-15). Petesi- purpura 46 hastada (% 100), artrit- artralji 25 hastada (% 54,3), gastrointestinal sistem tutulumu 27 hastada (% 58,6), renal tutulum 15 hastada (% 32,6) gozlendi.SonucHSP genelde hafif seyirli ve kendini sinirlayan bir hastalik olup nadiren kronik bobrek yetmezligine yol acabilir. HSP'nin uzun donem morbiditesi renal tutulumla iliskilidir. HSP'li her cocuk tanidan itibaren 1 yil boyunca periodik olarak tam idrar analizi yaptirmalidir.
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