Korean J Hematol 2004; 39(1):

Published online March 31, 2004

© The Korean Society of Hematology

복부 대동맥 혈전증의 소견을 보이는 원발성항인지질증후군 1례

박정진, 이정찬, 송영욱

경상대학교 의과대학 내과학교실,
서울대학교 의과대학 내과학교실

Abdominal Aortic Thrombosis as the Manifestation of the Primary Antiphospholipid Syndrome

Jeong Jin Park, Jung Chan Lee, Yeong Wook Song

Department of Internal Medicine, College of Medicine, Gyeongsang National University, Jinju, Korea
Seoul National University, Seoul, Korea

Abstract

Antiphospholipid syndrome (APS) is an autoimmune hypercoagulability syndrome. The clinical feature of the antiphospholipid syndrome is characterized by venous or arterial thromboses, recurrent fetal losses and/or thrombocytopenia with evidence of antiphospholipid antibodies, namely lupus anticoagulant, anticardiolipin antibodies. Although APS is most commonly associated with systemic lupus erythematosus or related autoimmune disease (secondary APS), APS also has been identified in patients with vaso-occlusive disease without any other manifestations of connective tissue disease (primary APS). In primary APS, aortic thrombosis has been rarely reported. We report a case of thrombosis of abdominal aorta in primary APS.

Keywords Antiphospholipid syndrome, Thrombosis, Abdominal aorta

Article

Korean J Hematol 2004; 39(1): 51-54

Published online March 31, 2004

Copyright © The Korean Society of Hematology.

복부 대동맥 혈전증의 소견을 보이는 원발성항인지질증후군 1례

박정진, 이정찬, 송영욱

경상대학교 의과대학 내과학교실,
서울대학교 의과대학 내과학교실

Abdominal Aortic Thrombosis as the Manifestation of the Primary Antiphospholipid Syndrome

Jeong Jin Park, Jung Chan Lee, Yeong Wook Song

Department of Internal Medicine, College of Medicine, Gyeongsang National University, Jinju, Korea
Seoul National University, Seoul, Korea

Abstract

Antiphospholipid syndrome (APS) is an autoimmune hypercoagulability syndrome. The clinical feature of the antiphospholipid syndrome is characterized by venous or arterial thromboses, recurrent fetal losses and/or thrombocytopenia with evidence of antiphospholipid antibodies, namely lupus anticoagulant, anticardiolipin antibodies. Although APS is most commonly associated with systemic lupus erythematosus or related autoimmune disease (secondary APS), APS also has been identified in patients with vaso-occlusive disease without any other manifestations of connective tissue disease (primary APS). In primary APS, aortic thrombosis has been rarely reported. We report a case of thrombosis of abdominal aorta in primary APS.

Keywords: Antiphospholipid syndrome, Thrombosis, Abdominal aorta

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