Long-Term Anticoagulation Therapy for Antiphospholipid Syndrome Following Unsuccessful Arterial Thrombosis Stent Procedure: A Case Report

Antiphospholipid syndrome (APS) is an autoimmune, multisystemic disorder marked by arterial, venous, or small-vessel thromboembolic events and persistence of antiphospholipid antibodies (aPL). Approximately 50% of APS patients exhibit primary disease features, while the remainder present with concur...

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Main Author: Hyun Sik Kang (Author)
Format: Book
Published: The Korean Society of Pediatric Hematology-Oncology, 2023-04-01T00:00:00Z.
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100 1 0 |a Hyun Sik Kang  |e author 
245 0 0 |a Long-Term Anticoagulation Therapy for Antiphospholipid Syndrome Following Unsuccessful Arterial Thrombosis Stent Procedure: A Case Report 
260 |b The Korean Society of Pediatric Hematology-Oncology,   |c 2023-04-01T00:00:00Z. 
500 |a 2233-5250 
500 |a 10.15264/cpho.2023.30.1.36 
520 |a Antiphospholipid syndrome (APS) is an autoimmune, multisystemic disorder marked by arterial, venous, or small-vessel thromboembolic events and persistence of antiphospholipid antibodies (aPL). Approximately 50% of APS patients exhibit primary disease features, while the remainder present with concurrent systemic autoimmune conditions. Venous thromboses are more common than arterial thromboses, with the latter primarily developing within the cerebral arteries, as in transient ischemic attacks or strokes. The incidence of thrombosis is higher in cases of APS with systemic lupus erythematosus than in primary APS. Thrombocytopenia, observed in 20-40% of APS patients, is generally moderate, asymptomatic, and does not require intervention. Thrombosis may be linked to autoimmune hemolysis, both of which are associated with aPL. Triple positivity, a high-risk serological profile, including lupus erythematosus, anti-cardiolipin antibodies, and anti-B2 glycoprotein I antibodies, is related to aPL. Positive results for all three serologic tests significantly increase thrombosis risk, necessitating continuous aspirin and warfarin use to mitigate risk. We here report a case involving a 15-year-old girl with triple-positive APS who underwent unsuccessful thrombolysis and balloon catheter dilation procedures and required long-term arterial thrombosis treatment with aspirin and warfarin. 
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546 |a KO 
690 |a adolescent 
690 |a antiphospholipid syndrome 
690 |a lupus erythematosus 
690 |a systemic 
690 |a thrombosis 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Neoplasms. Tumors. Oncology. Including cancer and carcinogens 
690 |a RC254-282 
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786 0 |n Clinical Pediatric Hematology-Oncology, Vol 30, Iss 1, Pp 36-41 (2023) 
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