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Rheumatology 2003; 42: 200-213
© 2003 British Society for Rheumatology


Review

Central nervous system involvement in the antiphospholipid (Hughes) syndrome

G. Sanna1, M. L. Bertolaccini1, M. J. Cuadrado1,2, M. A. Khamashta1, and G. R. V. Hughes1

1 Lupus Research Unit, The Rayne Institute, St Thomas' Hospital, London, UK and
2 Rheumatology Department, Reina Sofia University Hospital, Cordoba, Spain

The antiphospholipid (Hughes) syndrome (APS) is characterized by arterial and/or venous thrombosis and pregnancy morbidity in the presence of anticardiolipin antibodies and/or lupus anticoagulant. APS can occur either as a primary disorder or secondary to a connective tissue disease, most frequently systemic lupus erythematosus. Central nervous system (CNS) involvement is one of the most prominent clinical manifestations of APS, and includes arterial and venous thrombotic events, psychiatric features and a variety of other non-thrombotic neurological syndromes. In this review we focus on the common and some of the less common CNS manifestations that have been reported in association with antiphospholipid antibodies.

Correspondence to: M. A. Khamashta, Lupus Research Unit, The Rayne Institute, St Thomas' Hospital, London SE1 7EH, UK. E-mail: munther.khamashta{at}kcl.ac.uk


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