Lupus anticoagulant-hypoprothrombinemia syndrome and catastrophic antiphospholipid syndrome in a patient with antidomain I antibodies

被引:6
|
作者
Galland, Joris [1 ,2 ]
Mohamed, Shirine [1 ,2 ]
Revuz, Sabine [1 ,2 ]
de Maistre, Emmanuel [3 ]
de Laat, Bas [4 ]
Marie, Pierre-Yves [5 ,6 ,7 ]
Zuily, Stephane [1 ,2 ,6 ,7 ]
Levy, Bruno [6 ,7 ]
Regnault, Veronique [7 ]
Wahl, Denis [1 ,2 ,6 ,8 ]
机构
[1] Nancy Univ Hosp, Vasc Med Div, Nancy, France
[2] Ctr Rare Vasc & Syst Autoimmune Dis, Reg Competence, Nancy, France
[3] Dijon Univ Hosp, Haematol Lab, Dijon, France
[4] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Biochem, Maastricht, Netherlands
[5] Nancy Univ Hosp, Nucl Med & Nancyclotep Expt Imaging, Platform, Nancy, France
[6] Univ Lorraine, Nancy, France
[7] INSERM, UMR S 1116, Nancy, France
[8] Nancy Univ Hosp, Dept Crit Care Med, Nancy, France
关键词
antidomain I antibodies; catastrophic antiphospholipid antibody syndrome; lupus anticoagulant-hypoprothrombinemia syndrome; systemic lupus erythematosus;
D O I
10.1097/MBC.0000000000000545
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lupus anticoagulant-hypoprothrombinemia syndrome is a rare condition characterized by the association of acquired factor II deficiency and lupus anticoagulant. Contrary to classical antiphospholipid syndrome, it may cause severe life-threatening bleeding (89% of published cases). We report a patient, positive for antidomain I antibodies, with initially primary lupus anticoagulant-hypoprothrombinemia syndrome without previous clinical manifestation or underlying systemic disease. Five years later, he experienced the first systemic lupus erythematous flare. Within a few days, catastrophic antiphospholipid syndrome was diagnosed with heart, liver and kidney involvement. The patient recovered under pulse steroids, intravenous heparin and intravenous immunoglobulins. Copyright (C) 2016 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:580 / 582
页数:3
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