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NDT Advance Access originally published online on January 18, 2006
Nephrology Dialysis Transplantation 2006 21(6):1734-1735; doi:10.1093/ndt/gfk091
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© The Author [2006]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Letter

Fatal relapse of thrombotic thrombocytopaenic purpura after cardiac surgery in patient with congenital absence of vWF-cleaving protease activity

Email: nina_basic@net.hr

The first 10% of the full text of this article appears below.

Sir,

Thrombotic thrombocytopaenic purpura (TTP) is a relatively rare disorder, commonly described with the pentad of thrombocytopaenia, microangiopatic haemolytic anaemia, mental status deterioration, renal failure and fever. Although it is well known that virtually every organ may be affected by TTP, cardiac involvement is rarely reported in the TTP literature [1–6]. With the present case we would like to highlight two significant and neglected problems in patients with TTP: cardiac involvement . . . [Full Text of this Article]

Nikolina Basic-Jukic, Petar Kes and Bruna Brunetta

Clinical hospital Zagreb Department of dialysis Zagreb Croatia (Hrvatska)


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