Journal article
Thrombotic thrombocytopenic purpura: 2008 update.
Abstract
Thrombotic thrombocytopenic purpura (TTP) is a spectrum of syndromes characterized by thrombocytopenia and microangiopathic hemolytic anemia, manifested by an elevated blood lactate dehydrogenase (LDH) concentration and red blood cell fragments. It classically occurs in patients with a hereditary or acquired lack of ADAMTS13, a metalloproteinase that cleaves large multimers of von Willebrand factor. Other TTP-like syndromes, including TTP …
Authors
Crowther MA; George JN
Journal
Cleveland Clinic Journal of Medicine, Vol. 75, No. 5, pp. 369–375
Publisher
Cleveland Clinic Journal of Medicine
Publication Date
May 1, 2008
DOI
10.3949/ccjm.75.5.369
ISSN
0891-1150