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上肢深静脉血栓形成中的高凝状态。

Hypercoagulability states in upper-extremity deep venous thrombosis.

作者信息

Leebeek F W, Stadhouders N A, van Stein D, Gómez-García E B, Kappers-Klunne M C

机构信息

University Hospital Rotterdam "Dijkzigt", Department of Hematology, Rotterdam, The Netherlands.

出版信息

Am J Hematol. 2001 May;67(1):15-9. doi: 10.1002/ajh.1070.

Abstract

Deep venous thrombosis of the upper extremity (DVTUE) is a rare thrombotic disorder that may occur spontaneously but is most often related to predisposing factors, such as an indwelling central venous catheter, malignancy, or exercise. The role of coagulation disorders, i.e., a hypercoagulable state in the pathogenesis of DVTUE is not well known. We have evaluated both genetic and acquired thrombophilia parameters in consecutive patients with DVTUE. A hypercoagulable state was found in 32% of the patients. The most frequent coagulation abnormality was the presence of lupus anticoagulant or anticardiolipin antibodies (27%). Factor V Leiden mutation was detected in two patients, antithrombin deficiency in one, and none of the patients had the prothrombin G20210A gene variant or protein C or S deficiency. The prevalence of coagulation abnormalities was not significantly different in a subgroup of patients with spontaneous DVTUE as compared to those with an obvious predisposing factor, such as an indwelling central venous catheter. We conclude that antiphospholipid antibodies are frequently found in patients with DVTUE. Factor V Leiden mutation, prothrombin 20210A gene variant, protein C deficiency, and protein S deficiency do not seem to play a major pathogenetic role in DVTUE.

摘要

上肢深静脉血栓形成(DVTUE)是一种罕见的血栓性疾病,可自发发生,但最常与诱发因素有关,如留置中心静脉导管、恶性肿瘤或运动。凝血障碍,即高凝状态在DVTUE发病机制中的作用尚不清楚。我们对连续的DVTUE患者的遗传和获得性易栓症参数进行了评估。32%的患者存在高凝状态。最常见的凝血异常是狼疮抗凝物或抗心磷脂抗体的存在(27%)。两名患者检测到因子V莱顿突变,一名患者抗凝血酶缺乏,且没有患者有凝血酶原G20210A基因变异或蛋白C或S缺乏。与有明显诱发因素(如留置中心静脉导管)的患者亚组相比,自发性DVTUE患者亚组中凝血异常的患病率没有显著差异。我们得出结论,抗磷脂抗体在DVTUE患者中经常被发现。因子V莱顿突变、凝血酶原20210A基因变异、蛋白C缺乏和蛋白S缺乏似乎在DVTUE的发病机制中不发挥主要作用。

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