منابع مشابه
Rivaroxaban to treat thrombotic antiphospholipid syndrome.
Thrombosis is one of the clinical hallmarks of antiphospholipid syndrome, a heterogeneous autoimmune disorder associated with the presence of antiphospholipid antibodies. Thrombosis can occur in any vascular bed, but most patients present with venous thrombosis or ischaemic stroke. Patients with antiphospholipid syndrome have a high risk of recurrent thrombotic events. The standard treatment fo...
متن کاملThrombotic microangiopathic haemolytic anaemia and antiphospholipid antibodies.
OBJECTIVE To analyse the clinical and laboratory features of patients with thrombotic microangiopathic haemolytic anaemia (TMHA) associated with antiphospholipid antibodies (aPL). METHODS A computer assisted (PubMed) search of the literature was performed to identify all cases of TMHA associated with aPL from 1983 to December 2002. RESULTS 46 patients (36 female) with a mean (SD) age at pre...
متن کاملAnticardiolipin syndrome: antiphospholipid syndrome.
North Am 2000;26:215–27. 14 Savill J. Recognition and phagocytosis of cells undergoing apoptosis. Br Med Bull 1997;53:491–508. 15 Elkon KB. Apoptosis in SLE – too little or too much? Review. Clin Exp Rheumatol 1994;12:553–9. 16 Drappa J, Vaishnaw AK, Sullivan KE, Chu JL, Elkon KB. Fas gene-mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmu...
متن کاملAntiphospholipid syndrome
APS can be primary or secondary. Primary antiphospholipid syndrome occurs in the absence of any other related disease. Secondary antiphospholipid syndrome is often associated with systemic lupus erythematosus and less frequently with infections, drugs and other diseases. Serologic markers are antiphospholipid antibodies, lupus anticoagulant and anticardiolipin. In rare cases, APS leads to rapid...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Lupus
سال: 2018
ISSN: 0961-2033,1477-0962
DOI: 10.1177/0961203318801686