Marine Demoy, Julien Labrousse, François Grand, Stéphanie Moyrand, Marie Tuffigo, Solene Lamarche, Laurent Macchi
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引用次数: 0
摘要
虽然在法国发现了两组病例,但体质性 XI 因子缺乏症是一种罕见的疾病。获得性 XI 因子缺乏症极为罕见。XI 因子缺乏症的治疗并不简单,因为其出血倾向难以预测,与 XI 因子水平的关系并不明显。在评估出血倾向时,必须考虑其他止血参数。我们报告了先天性 XI 因子缺乏症、后天性 XI 因子缺乏症和与 XI 因子缺乏症相关的 von Willebrand 病的病例。另一方面,一些干扰因素会导致因子 XI 被低估,我们报告了狼疮抗凝剂干扰的病例。本综述旨在更好地了解如何处理因子 XI 水平降低的问题。
[Factor XI deficiency: actuality and review of the literature].
Although two clusters have been identified in France, constitutional factor XI deficiency is a rare disorder. Acquired factor XI deficiency is extremely rare. The management of factor XI deficiency is not staightforward because of the unpredictable bleeding tendency that does not clearly relate to the factor XI level. Other haemostastis parameters have to be taken into account to evaluate the bleeding tendency. We report the cases of a congenital factor XI deficiency, an acquired factor XI deficiency and a von Willebrand disease associated to a factor XI deficiency. On the other hand, some interferences can lead to underestimation of factor XI and we report the case of an interference by lupus anticoagulant. The objective of this review is to better understand how to manage a reduced factor XI level.