Warkentin T E
McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Ann Intern Med. 2001 Oct 16;135(8 Pt 1):589-93. doi: 10.7326/0003-4819-135-8_part_1-200110160-00009.
The cause of cancer-associated venous limb gangrene is unknown but could paradoxically be due to warfarin.
To determine the pathogenesis of venous gangrene in a patient with cancer.
Case report.
University hospital in Ontario, Canada.
66-year-old woman with metastatic lung cancer and deep venous thrombosis.
Levels of vitamin K-dependent factors, additional coagulation factors, and thrombin-antithrombin complexes (marker of thrombin generation).
During warfarin use, venous limb gangrene developed when the international normalized ratio (INR) reached 6.0 (therapeutic range, 2.0 to 3.0); at this time, the level of protein C (a vitamin K-dependent natural anticoagulant) was severely reduced, but thrombin-antithrombin complexes remained markedly elevated. The supratherapeutic INR was explained by the greatly reduced levels of factor VII, which correlated closely with protein C levels; therefore, the high INR was a surrogate marker for severely reduced protein C activity.
Warfarin may contribute to the pathogenesis of cancer-associated venous limb gangrene by leading to severe depletion of protein C while at the same time failing to reduce thrombin generation.
癌症相关的静脉性肢体坏疽病因不明,但矛盾的是可能与华法林有关。
确定一名癌症患者静脉坏疽的发病机制。
病例报告。
加拿大安大略省的大学医院。
一名66岁患有转移性肺癌和深静脉血栓形成的女性。
维生素K依赖因子、其他凝血因子以及凝血酶 - 抗凝血酶复合物(凝血酶生成的标志物)水平。
在使用华法林期间,当国际标准化比值(INR)达到6.0(治疗范围为2.0至3.0)时发生了静脉性肢体坏疽;此时,蛋白C(一种维生素K依赖的天然抗凝剂)水平严重降低,但凝血酶 - 抗凝血酶复合物仍显著升高。超治疗范围的INR是由于因子VII水平大幅降低所致,其与蛋白C水平密切相关;因此,高INR是蛋白C活性严重降低的替代标志物。
华法林可能通过导致蛋白C严重耗竭,同时又未能减少凝血酶生成,从而促使癌症相关静脉性肢体坏疽的发病机制。