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一名同时患有因子V莱顿突变和狼疮抗凝物的年轻患者发生自发性静脉血栓形成。

Spontaneous venous thrombosis in a young patient with combined factor V Leiden and lupus anticoagulant.

作者信息

Lopez F F, Sweeney J D, Blair A J, Sikov W M

机构信息

The Miriam Hospital, Brown University School of Medicine, Providence, Rhode Island 02906, USA.

出版信息

Am J Hematol. 1999 Sep;62(1):58-60. doi: 10.1002/(sici)1096-8652(199909)62:1<58::aid-ajh11>3.0.co;2-0.

Abstract

We describe a case of a 28-year-old man who developed an extensive spontaneous deep venous thrombosis. Testing revealed heterozygotic factor V Leiden mutation, and the presence of both lupus anticoagulant (LA) and elevated IgM anticardiolipin antibody (ACA). Several family members were found to be heterozygous for factor V Leiden. A paternal aunt had the factor V Leiden mutation, an elevated plasma homocysteine and a borderline increased IgG ACA level. No other family member had a history of a venous thrombotic event. This case illustrates that evaluation of young patients who present with venous thrombosis should be performed for both hereditary and acquired thrombophilic defects. The family studies suggest that the presence of a lupus anticoagulant may be more clinically significant than elevated ACA in risk assessment. Although screening family members when the proband carries factor V Leiden is controversial, psychological reassurance of those who test negative and simple advice on occupations or social habits (e.g., smoking) for those who test positive may be important benefits.

摘要

我们描述了一例28岁男性发生广泛自发性深静脉血栓形成的病例。检测发现其存在杂合子因子V莱顿突变,同时存在狼疮抗凝物(LA)及IgM抗心磷脂抗体(ACA)升高。发现数名家庭成员为因子V莱顿杂合子。一位姑姑存在因子V莱顿突变、血浆同型半胱氨酸升高及临界升高的IgG ACA水平。没有其他家庭成员有静脉血栓形成事件史。该病例表明,对于出现静脉血栓形成的年轻患者,应评估其遗传性和获得性易栓缺陷。家族研究提示,在风险评估中,狼疮抗凝物的存在可能比ACA升高更具临床意义。虽然当先证者携带因子V莱顿突变时筛查家庭成员存在争议,但对检测阴性者给予心理安慰,对检测阳性者就职业或社会习惯(如吸烟)给予简单建议可能会带来重要益处。

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