| Literature DB >> 15592692 |
Martial Koenig1, Michel Roy, Sylviane Baccot, Muriel Cuilleron, Jean-Pierre de Filippis, Pascal Cathébras.
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.Entities:
Mesh:
Year: 2004 PMID: 15592692 DOI: 10.1007/s10067-004-1017-1
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980