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Korean Journal of Pediatric Hematology-Oncology ; : 239-244, 2002.
Article in Korean | WPRIM | ID: wpr-59291

ABSTRACT

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.


Subject(s)
Female , Humans , Infant , Antibodies, Anticardiolipin , Antibodies, Antiphospholipid , Antiphospholipid Syndrome , Autoantibodies , Autoimmune Diseases , Brain , Communicable Diseases , Dexamethasone , Enzyme-Linked Immunosorbent Assay , Exanthema , Extremities , Fever , Lateral Sinus Thrombosis , Lupus Erythematosus, Systemic , Lymph Nodes , Magnetic Resonance Imaging , Meningitis , Mucocutaneous Lymph Node Syndrome , Necrosis , Partial Thromboplastin Time , Phospholipids , Skin , Thrombosis , Thrombotic Microangiopathies , Toes
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