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1
A new coagulation defect associated with a case of melanomatosis.与一例黑素瘤病相关的一种新的凝血缺陷。
J Clin Pathol. 1977 Jun;30(6):547-50. doi: 10.1136/jcp.30.6.547.
2
Activation of Hageman factor in the nephrotic syndrome.肾病综合征中Hageman因子的激活。
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The first cases of Fitzgerald factor deficiency in the Orient: three cases in one family.东方首例菲茨杰拉德因子缺乏症:一个家族中的三例病例。
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Why factor XI deficiency is a clinical concern.为什么因子 XI 缺乏症是一个临床关注点。
Expert Rev Hematol. 2016 Jul;9(7):629-37. doi: 10.1080/17474086.2016.1191944. Epub 2016 Jun 24.
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[Defects in the intrinsic pathway of the coagulation system].[凝血系统内源性途径中的缺陷]
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Presse Med (1893). 1968 Nov 23;76(45):2161-2.
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The enigma of severe factor XI deficiency without hemmorrhagic symptoms. Distinction from Hageman factor and "Fletcher factor" deficiency; family study; and problems of diagnosis.无出血症状的重度因子XI缺乏之谜。与激肽释放酶原和“弗莱彻因子”缺乏的鉴别;家系研究;以及诊断问题。
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引用本文的文献

1
Hemostatic changes in patients with malignancy.恶性肿瘤患者的止血变化。
Int J Hematol. 2001 Feb;73(2):151-6. doi: 10.1007/BF02981931.

本文引用的文献

1
The relation of 'Fletcher Factor' to factors XI and XII.“弗莱彻因子”与因子XI和因子XII的关系。
Br J Haematol. 1970 Feb;18(2):161-9. doi: 10.1111/j.1365-2141.1970.tb01431.x.
2
Fletcher factor deficiency: family study and detection.弗莱彻因子缺乏症:家族研究与检测
Blood. 1974 May;43(5):641-4.
3
A hitherto undescribed plasma factor acting at the contact phase of blood coagulation (Flaujeac factor): case report and coagulation studies.一种作用于血液凝固接触阶段的此前未被描述的血浆因子(弗洛热阿克因子):病例报告及凝血研究
Blood. 1975 Nov;46(5):761-8.
4
The effect of increased contact activation time on the activated partial thromboplastin time.接触激活时间延长对活化部分凝血活酶时间的影响。
Am J Clin Pathol. 1976 Sep;66(3):479-82. doi: 10.1093/ajcp/66.3.479.
5
A new method for the assay of factor XI in plasma and the preparation and use of a new artificial substrate.一种用于测定血浆中因子 XI 的新方法以及一种新型人工底物的制备与应用。
J Clin Pathol. 1975 Apr;28(4):332-6. doi: 10.1136/jcp.28.4.332.

与一例黑素瘤病相关的一种新的凝血缺陷。

A new coagulation defect associated with a case of melanomatosis.

作者信息

Phillips J D, O'Shea M J

出版信息

J Clin Pathol. 1977 Jun;30(6):547-50. doi: 10.1136/jcp.30.6.547.

DOI:10.1136/jcp.30.6.547
PMID:874111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC476466/
Abstract

A marked abnormality of the intrinsic coagulation system was observed in a patient with melanomatosis and frank melanuria. With successful treatment of the tumour there was a parallel improvement in the clotting abnormality. This defect was shown to be a deficiency of factor XI together with a previously unrecognised factor. This is distinct from either Fletcher or Fitzgerald factors and appears to act between factors XI and X in the coagulation sequence.

摘要

在一名患有黑素瘤病和明显黑尿症的患者中观察到内源性凝血系统存在显著异常。随着肿瘤的成功治疗,凝血异常也相应得到改善。结果表明,这种缺陷是由于缺乏因子XI以及一种先前未被识别的因子。这与弗莱彻因子或菲茨杰拉德因子均不同,并且似乎在凝血序列中作用于因子XI和因子X之间。