A Case of Primary Antiphospholipid Antibody Syndrome Showing Vegetation on the Mitral Valve Through Echocardiography

승모판에서 증식증(vegetation)이 확인된 원발성 항인지질 항체 증후군 1례

  • Lee, Seung-Yeop (Department of Neurology College of Medicine, Yeungnam University) ;
  • Park, Seung-Kwon (Department of Neurology College of Medicine, Yeungnam University) ;
  • Yun, Sung-Hwan (Department of Neurology College of Medicine, Yeungnam University) ;
  • Jung, Yun-Seok (Department of Neurology College of Medicine, Yeungnam University) ;
  • Kim, Hyen-Jik (Department of Neurology College of Medicine, Yeungnam University) ;
  • Lim, Sung-Hwan (Department of Neurology College of Medicine, Yeungnam University) ;
  • Hah, Jung-Sang (Department of Neurology College of Medicine, Yeungnam University) ;
  • Kim, Wook-Nyeun (Andong Presbyterian Hospital)
  • 이승엽 (영남대학교 의과대학 신경과학교실) ;
  • 박승권 (영남대학교 의과대학 신경과학교실) ;
  • 윤성환 (영남대학교 의과대학 신경과학교실) ;
  • 정윤석 (영남대학교 의과대학 신경과학교실) ;
  • 김현직 (영남대학교 의과대학 신경과학교실) ;
  • 임성환 (영남대학교 의과대학 신경과학교실) ;
  • 하정상 (영남대학교 의과대학 신경과학교실) ;
  • 김욱년 (안동 성소병원 신경과)
  • Published : 1998.12.30

Abstract

Antiphospholipid antibody syndrome(APS) is a well-known clinical syndrome characterized by recurrent arterial or venous thromboses, recurrent fetal loss, thrombocytopenia, together with high titers of sustained anticardiolipin antibody(aCL) or lupus anticoagulant(LA). Although systemic lupus erythematosus(SLB) and APS may coexist, a high proportion of patients manifesting the APS do not suffer from classical lupus or other connective tissue disease. The patient has been defined as having a primary antiphospholipid antibody syndrome. We experienced one case of primary APS with recurrent fetal loss, recurrent cerebral infarctions, positive anticardiolipin antibody IgG and fluttering vegetation on the mitral valve, without other connective tissue diseases including SLE. Forty-three old female had 2 out of 11 criteria for the diagnosis of SLE, such as thrombocytopenia and positive antinuclear antibody, but did not meet whole criteria. The patient was treated with ticlopidine, and anticoagulant therapy was recommended.

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