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Artigo em Coreano | WPRIM | ID: wpr-59291

RESUMO

Antiphospholipid antibodies are a family of autoantibodies directed against certain phospholipids or phospholipid-binding proteins. Antiphospholipid antibody syndrome can occur as a secondary event to an underlying autoimmune disease, most commonly systemic lupus erythematosus and also occur in certain infectious diseases and drug reactions. We experienced a patient with Kawasaki disease who had anticardiolipin antibodies accompanied by coagulation abnormalities. A 4-month-old female patient was admitted due to fever, irritability, lymph node swelling on the right submandibular area and maculopapular skin rashes on trunk and both extremities. She had prolonged activated partial thromboplastin time (aPTT). Further investigations revealed a positive anticardiolipin antibody detected by ELISA. She had right lateral sinus thrombosis on parieto-occipital area on brain MRI and thrombotic microangiopathy, resulting in necrosis of toe. She showed considerable improvement in affected skin after dexamethasone treatment for 3 weeks. Thrombosis was resolved completely 2 months later.


Assuntos
Feminino , Humanos , Lactente , Anticorpos Anticardiolipina , Anticorpos Antifosfolipídeos , Síndrome Antifosfolipídica , Autoanticorpos , Doenças Autoimunes , Encéfalo , Doenças Transmissíveis , Dexametasona , Ensaio de Imunoadsorção Enzimática , Exantema , Extremidades , Febre , Trombose do Seio Lateral , Lúpus Eritematoso Sistêmico , Linfonodos , Imageamento por Ressonância Magnética , Meningite , Síndrome de Linfonodos Mucocutâneos , Necrose , Tempo de Tromboplastina Parcial , Fosfolipídeos , Pele , Trombose , Microangiopatias Trombóticas , Dedos do Pé
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