[Multi-facetted clinical presentation of thrombotic thrombocytopenic purpura]

C.U. Niemann, J. Jurlander, G. Daugaard, L. Friis-Hansen

Abstract

Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathic disease. TTP is due to reduced activity of the von Willebrand factor which cleaves ADAMTS13. The disease is characterized by thrombocytopenia (<20 billion/l) intravascular Coombs-negative haemolysis and schistocytes in blood smears. Determination of the ADAMTS13-activity is now becoming available as a routine analysis. We present two cases that illustrate the multi-facetted clinical presentation under which TTP occurs. The importance of access to ADAMTS13 measurements is stressed
Udgivelsesdato: 2009/1/26
OriginalsprogDansk
TidsskriftUgeskrift for læger
Vol/bind171
Udgave nummer5
Sider (fra-til)340-342
Antal sider2
ISSN0041-5782
StatusUdgivet - 2009

Citationsformater