[Hemolytic uremic syndrome and thrombotic thrombocytopenic purpura].

نویسندگان

  • C Masset
  • B Dubois
  • G Rorive
چکیده

Hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are thrombotic microangiopathies (TMA). Both familial and sporadic forms exist: anaemia, thrombopaenia, renal failure and neurologic disorders are common clinical features. The differential diagnosis depends on plasma levels of von Willebrand factor-cleaving protease: there is a deficiency of this protease in patients with TTP whereas its rate is normal in HUS. We remind pathophysiology, etiologies and treatment of these TMA.

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عنوان ژورنال:
  • Revue medicale de Liege

دوره 57 1  شماره 

صفحات  -

تاریخ انتشار 2002