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      KCI등재 SCIE

      Lupus anticoagulant-hypoprothrombinemia in healthy adult

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      https://www.riss.kr/link?id=A103902402

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      다국어 초록 (Multilingual Abstract)

      The presence of lupus anticoagulant is associated with an elevated risk of venous and arterial thrombosis, and recurrent miscarriages as well. For some cases, this disease can present with bleeding as a consequence of lupus anticoagulant‐hypoprothro...

      The presence of lupus anticoagulant is associated with an elevated risk of venous and arterial thrombosis, and recurrent miscarriages as well. For some cases, this disease can present with bleeding as a consequence of lupus anticoagulant‐hypoprothrombinemia (LAHPS). LAHPS is a rare disease and it is reported to be most frequent in young females with/without systemic lupus erythematosus or in healthy children who are suffering with a viral infection. In such cases, steroid therapy is usually effective in normalizing the biological abnormalities and controlling the bleeding problems.
      A 34-year-old previously healthy man was admitted to our department because of his prolonged coagulation times; these abnormalities were discovered before performing orthopedic surgery. The prothrombin time (PT) was 15.2 sec, and the activated partial thromboplastin time (APTT) was 37.7 sec. A 1:1 dilution of patient plasma with normal plasma nearly corrected the PT, but this failed to correct the APTT. Evaluation of the clotting factors revealed decreased levels of factors II, V, VIII, IX and XI. The presence of LA was demonstrated by the dRVVT test, and the patient was diagnosed with LAHPS. He was successfully treated with corticosteroid before performing the orthopedic surgery.

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      다국어 초록 (Multilingual Abstract)

      The presence of lupus anticoagulant is associated with an elevated risk of venous and arterial thrombosis, and recurrent miscarriages as well. For some cases, this disease can present with bleeding as a consequence of lupus anticoagulant‐hypoprothro...

      The presence of lupus anticoagulant is associated with an elevated risk of venous and arterial thrombosis, and recurrent miscarriages as well. For some cases, this disease can present with bleeding as a consequence of lupus anticoagulant‐hypoprothrombinemia (LAHPS). LAHPS is a rare disease and it is reported to be most frequent in young females with/without systemic lupus erythematosus or in healthy children who are suffering with a viral infection. In such cases, steroid therapy is usually effective in normalizing the biological abnormalities and controlling the bleeding problems.
      A 34-year-old previously healthy man was admitted to our department because of his prolonged coagulation times; these abnormalities were discovered before performing orthopedic surgery. The prothrombin time (PT) was 15.2 sec, and the activated partial thromboplastin time (APTT) was 37.7 sec. A 1:1 dilution of patient plasma with normal plasma nearly corrected the PT, but this failed to correct the APTT. Evaluation of the clotting factors revealed decreased levels of factors II, V, VIII, IX and XI. The presence of LA was demonstrated by the dRVVT test, and the patient was diagnosed with LAHPS. He was successfully treated with corticosteroid before performing the orthopedic surgery.

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      참고문헌 (Reference)

      1 Lillquist KB, "The absence of Factor II in a child with systemic lupus erythematosus" 67 : 533-536, 1978

      2 Vivaldi P, "Severe bleeding due to acquired hypoprothrombinemia-lupus anticoagulant syndrome: case report and review of literature" 82 : 345-347, 1997

      3 Bernini JC, "Hypoprothrombinemia and severe hemorrhage associated with a lupus anticoagulant" 123 : 937-939, 1993

      4 Cuadrado MJ, "Hughes (antiphospholipid) syndrome: clinical features" 27 : 507-524, 2001

      5 Simel DL, "Correction of hypoprothrombinemia by immunosuppressive treatment of the lupus anticoagulant-hypoprothrombinemia syndrome" 83 : 563-566, 1987

      6 Follea G, "Antiprothrombinase and factor II deficiency in a non SLE patient" 46 : 670-, 1981

      7 Hift RJ, "Acquired hypoprothrombinaemia and lupus anticoagulant: response to steroid therapy" 30 : 308-310, 1991

      8 Bajaj SP, "A mechanism for the hypoprothrombinemia of the acquired hypothrombinemia-lupus anticoagulant syndrome" 61 : 684-692, 1983

      1 Lillquist KB, "The absence of Factor II in a child with systemic lupus erythematosus" 67 : 533-536, 1978

      2 Vivaldi P, "Severe bleeding due to acquired hypoprothrombinemia-lupus anticoagulant syndrome: case report and review of literature" 82 : 345-347, 1997

      3 Bernini JC, "Hypoprothrombinemia and severe hemorrhage associated with a lupus anticoagulant" 123 : 937-939, 1993

      4 Cuadrado MJ, "Hughes (antiphospholipid) syndrome: clinical features" 27 : 507-524, 2001

      5 Simel DL, "Correction of hypoprothrombinemia by immunosuppressive treatment of the lupus anticoagulant-hypoprothrombinemia syndrome" 83 : 563-566, 1987

      6 Follea G, "Antiprothrombinase and factor II deficiency in a non SLE patient" 46 : 670-, 1981

      7 Hift RJ, "Acquired hypoprothrombinaemia and lupus anticoagulant: response to steroid therapy" 30 : 308-310, 1991

      8 Bajaj SP, "A mechanism for the hypoprothrombinemia of the acquired hypothrombinemia-lupus anticoagulant syndrome" 61 : 684-692, 1983

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.37 0.26 1.02
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.83 0.73 0.566 0.13
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