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获得性血管性血友病综合征与游离λ轻链单克隆丙种球蛋白病、正常出血时间及对泼尼松的反应相关。

Acquired von Willebrand disease associated with free lambda light chain monoclonal gammopathy, normal bleeding time and response to prednisone.

作者信息

Stewart A K, Glynn M F

机构信息

Department of Medicine, Toronto General Hospital, University of Toronto, Ontario, Canada.

出版信息

Postgrad Med J. 1990 Jul;66(777):560-2. doi: 10.1136/pgmj.66.777.560.

Abstract

We report a case of acquired von Willebrand's syndrome with severe gastrointestinal bleeding and associated free monoclonal lambda light chains. The patient had a rapid sustained clinical and laboratory response to the administration of prednisone. Of note in this patient was the occurrence of angiodysplasia which has previously been reported in association with acquired von Willebrand's syndrome. No inhibitors of VWF:Ag, VWF:RCoF, or factor VIII:C were detected by mixing studies and the bleeding time was normal. Very few high molecular weight von Willebrand multimers were present prior to prednisone; however, the pattern reverted to a normal distribution following treatment. In appropriate patients with acquired von Willebrand's syndrome and monoclonal para-proteins, a trial of prednisone may be indicated.

摘要

我们报告一例获得性血管性血友病综合征,伴有严重胃肠道出血及相关游离单克隆λ轻链。该患者在使用泼尼松后临床和实验室指标迅速持续改善。该患者值得注意的是出现了血管发育异常,此前已有报道其与获得性血管性血友病综合征相关。混合试验未检测到血管性血友病因子抗原(VWF:Ag)、血管性血友病因子瑞斯托霉素辅因子(VWF:RCoF)或凝血因子VIII:C的抑制物,出血时间正常。在使用泼尼松之前,高分子量血管性血友病多聚体很少;然而,治疗后模式恢复为正常分布。对于有获得性血管性血友病综合征和单克隆副蛋白的合适患者,可能需要进行泼尼松试验。

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本文引用的文献

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Acquired von Willebrand's syndrome.获得性血管性血友病综合征
Br J Haematol. 1980 May;45(1):161-4. doi: 10.1111/j.1365-2141.1980.tb03821.x.
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IgA inhibitor to factor VIII/von Willebrand factor.
Br J Haematol. 1985 Jan;59(1):149-58. doi: 10.1111/j.1365-2141.1985.tb02975.x.

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