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因子 X 缺乏:AL 淀粉样变性的一种不常见表现。

Factor X deficiency: an uncommon presentation of AL amyloidosis.

机构信息

Emory University Hospital, 1364 Clifton Road NE, Atlanta, GA 30322, USA.

出版信息

Ups J Med Sci. 2012 Nov;117(4):457-9. doi: 10.3109/03009734.2012.690457. Epub 2012 Jun 1.

Abstract

Factor X deficiency is the most common coagulation factor deficiency amongst patients with AL amyloidosis. It presumably occurs due to adsorption of factor X to amyloid fibrils. The deficiency of this factor, in conjunction with other hemostatic defects, can cause bleeding complications. A case of acquired factor X deficiency due to AL amyloidosis is reported, where abnormal coagulation parameters were the only presenting feature.

摘要

因子 X 缺乏症是 AL 淀粉样变性患者中最常见的凝血因子缺乏症。它可能是由于因子 X 吸附到淀粉样纤维上而发生的。这种因子的缺乏,加上其他止血缺陷,可能导致出血并发症。报告了一例由 AL 淀粉样变性引起的获得性因子 X 缺乏症,其中异常的凝血参数是唯一的表现特征。

相似文献

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Factor X deficiency: an uncommon presentation of AL amyloidosis.因子 X 缺乏:AL 淀粉样变性的一种不常见表现。
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本文引用的文献

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AL amyloidosis combined with acquired factor V deficiency.AL淀粉样变性合并获得性凝血因子V缺乏症。
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Factor-X deficiency in amyloidosis: a critical review.
Am J Hematol. 1981 Dec;11(4):443-50. doi: 10.1002/ajh.2830110414.

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