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Published in: Clinical Rheumatology 2/2005

01-04-2005 | Case Report

Thrombotic microangiopathy with liver, gut, and bone infarction (catastrophic antiphospholipid syndrome) associated with HELLP syndrome

Authors: Martial Koenig, Michel Roy, Sylviane Baccot, Muriel Cuilleron, Jean-Pierre de Filippis, Pascal Cathébras1

Published in: Clinical Rheumatology | Issue 2/2005

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Abstract

Hemolysis, elevated liver enzymes, low platelet count (HELLP) syndrome is a thrombotic microangiopathy complicating pregnancy and shares many clinical and biological features with thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS). Thrombotic microangiopathy is also a pathological feature of catastrophic antiphospholipid syndrome (CAPS). An association between refractory HELLP syndrome and antiphospholipid syndrome (APS) has been reported in a few cases. We describe a 19-year-old woman with APS and multiorgan failure conforming to a diagnosis of CAPS who developed refractory HELLP syndrome.
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Metadata
Title
Thrombotic microangiopathy with liver, gut, and bone infarction (catastrophic antiphospholipid syndrome) associated with HELLP syndrome
Authors
Martial Koenig
Michel Roy
Sylviane Baccot
Muriel Cuilleron
Jean-Pierre de Filippis
Pascal Cathébras1
Publication date
01-04-2005
Publisher
Springer-Verlag
Published in
Clinical Rheumatology / Issue 2/2005
Print ISSN: 0770-3198
Electronic ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-004-1017-1

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