rss
Ann Rheum Dis 64:943-946 doi:10.1136/ard.2004.026377
  • Concise report

Disseminated intravascular coagulation in catastrophic antiphospholipid syndrome: clinical and haematological characteristics of 23 patients

Table 2

 Differential diagnosis of multiorgan thrombotic disorders

Catastrophic APS DIC TMHA
*In cases of familial thrombocytopenic purpura (TTP), acquired idiopathic TTP, and pregnancy related TTP.
ADAMTS-13, von Willebrand factor cleaving protease; APS, antiphospholipid syndrome; DIC, disseminated intravascular coagulation; TMHA, thrombotic microangiopathic haemolytic anaemia.
Haemorrhagic manifestations + ±
Anaemia ± ± +
Schistocytes ± ± ++
Thrombocytopenia ++ ++ +++
Prolonged prothrombin time +
Prolonged activated partial thromboplastin time ± +
Fibrinogen degradation products ± +
Antiphospholipid antibodies ++ ± ±
Plasma ADAMTS-13 activity Normal? Moderately reduced Absent* or severely reduced

This Article

Register for free content


Free sample
This recent issue is free to all users to allow everyone the opportunity to see the full scope and typical content of ARD.
View free sample issue >>

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

  • Latest Rheumatology Jobs

    Rheumatology Jobs