Von Willebrand hastalığı’nda oral cerrahi yaklaşım: olgu sunumu
Abstract
Von Willebrand Disease (VWD) is a hereditary coagulation disorder characterized by a deficient or abnormal plasma protein known as the von Willebrand factor (vWF). Patients with VWD usually manifest a dual hemostatic defect characterized by a prolonged bleeding time and low plasma levels of Factor VIII coagulant activity. In the present case, management of 39 years old female patient with VWD in whom cryoprecipitate transfusion was applied for multiple tooth extractions was reported and alternative treatment protocols were discussed.
ÖZET
Von Willebrand Hastalığı (VWH), von Willebrand faktör (vWF) olarak bilinen plazma proteinin yetersiz ya da anormal şekilde bulunması ile karakterize herediter koagülasyon bozukluğudur. VWH olan hastalar, genellikle uzamış kanama zamanı ve Faktör VIII koagülasyon aktivitesinin düşük plazma değerleri ile karakterize ikili bir hemostatik defekte sahiptirler. Bu olgu raporunda, kliniğimize VWH tanısı ile başvuran 39 yaşındaki bayan hastanın, kriyospitat replasman tedavisi ile çoklu diş çekimleri gerçekleştirilip, alternatif tedavi protokolleri tartışılmıştır.
Anahtar kelimeler: Von Willebrand Hastalığı, diş çekimi
Keywords
References
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Details
Primary Language
English
Subjects
-
Journal Section
-
Authors
Ediz Deniz
Ahmet Arslan
Publication Date
November 11, 2011
Submission Date
November 11, 2011
Acceptance Date
-
Published in Issue
Year 1970 Volume: 11 Number: 1