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一种可能的双重杂合子II型血管性血友病,瑞斯托霉素诱导的血小板聚集增加。

A probable double heterozygous type II von Willebrand's disease with increased ristocetin induced platelet aggregation.

作者信息

Kinoshita S, Yoshioka K, Kasahara M, Takamiya O

机构信息

Department of Pediatrics, Osaka National Hospital, Japan.

出版信息

Am J Hematol. 1992 Jul;40(3):192-8. doi: 10.1002/ajh.2830400307.

Abstract

We have identified a patient with von Willebrand's disease (vWD) resembling type IIB vWD, with increased ristocetin induced platelet aggregation (RIPA), the absence of the large multimers of von Willebrand factor (vWF) in plasma, and the presence of the large multimers in platelets in whom a family study indicated a probable double heterozygous inheritance pattern. The propositus was a 12-year-old boy with frequent epistaxis and bruising. Abnormal hemostatic findings included a prolonged bleeding time (BT), decreased levels of factor VIII coagulant activity (VIIIC), von Willebrand factor antigen (vWF:Ag), ristocetin cofactor (RCof), and an increased RIPA. In the presence of ristocetin, binding of the patient's plasma vWF to normal platelets was increased but binding of normal vWF to his platelets was normal. SDS-agarose gel (1.5%) electrophoresis revealed that plasma vWF lacked the large multimers, and 3.0% gel electrophoresis revealed that the multimers had a 5-band pattern similar to normal. The above findings were consistent with type IIB vWD, but 1-deamino[8-D-arginine]-vasopressin (DDAVP) infusion resulted in a shortened BT and the transient appearance of large multimers without a decrease in the platelet count. Family studies revealed that his mother has mild bleeding symptoms, decreased VIIIC, vWF:Ag, and RCof levels and normal to slightly reduced RIPA with a multimer pattern consistent with type I vWD. In contrast, the father, sister, and paternal grandfather were asymptomatic, with a slightly decreased VIIIC level but a normal BT and vWF:Ag and RCof levels. Their RIPA and vWF binding to normal platelets were increased, but unlike the propositus their plasma contained large multimers. We concluded that the propositus is a type IIB-like variant differing from previously reported IIB variants in two ways: 1) his response to DDAVP and 2) a possible double heterozygous mode of inheritance rather than the usual dominant route.

摘要

我们发现了一名患有类似IIB型血管性血友病(vWD)的患者,其瑞斯托霉素诱导的血小板聚集(RIPA)增加,血浆中血管性血友病因子(vWF)的大分子量多聚体缺失,而血小板中存在大分子量多聚体,家系研究表明可能存在双杂合遗传模式。先证者是一名12岁男孩,经常鼻出血和出现瘀斑。异常的止血检查结果包括出血时间(BT)延长、凝血因子VIII促凝活性(VIIIC)、血管性血友病因子抗原(vWF:Ag)、瑞斯托霉素辅因子(RCof)水平降低以及RIPA增加。在有瑞斯托霉素存在的情况下,患者血浆vWF与正常血小板的结合增加,但正常vWF与他的血小板的结合正常。SDS - 琼脂糖凝胶(1.5%)电泳显示血浆vWF缺乏大分子量多聚体,而3.0%凝胶电泳显示多聚体具有与正常相似的5条带模式。上述发现与IIB型vWD一致,但注射1 - 去氨基[8 - D - 精氨酸] - 血管加压素(DDAVP)导致BT缩短以及大分子量多聚体短暂出现,且血小板计数未降低。家系研究显示,他的母亲有轻度出血症状,VIIIC、vWF:Ag和RCof水平降低,RIPA正常至略有降低,多聚体模式与I型vWD一致。相比之下,父亲、姐姐和祖父均无症状,VIIIC水平略有降低,但BT、vWF:Ag和RCof水平正常。他们的RIPA以及vWF与正常血小板的结合增加,但与先证者不同的是,他们的血浆中含有大分子量多聚体。我们得出结论,先证者是一种类似IIB型的变异型,在两个方面与先前报道的IIB型变异型不同:1)他对DDAVP的反应;2)可能是双杂合遗传模式而非通常的显性遗传途径。

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