Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.

Pathophysiology of Haemostasis and Thrombosis Pub Date : 2010-01-01 Epub Date: 2010-07-20 DOI:10.1159/000319051
Jasna Lenicek Krleza, Gordana Jakovljevic, Ana Bronic, Désirée Coen Herak, Aleksandra Bonevski, Jasminka Stepan-Giljevic, Goran Roic
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引用次数: 8

Abstract

We present the case of a 17-year-old girl who suddenly woke up with localized pain in the left groin and the inability to twist her leg. After comprehensive physician and laboratory examinations, deep venous thrombosis with consequent pulmonary embolism was ascertained. She had not experienced any recent trauma, but she had started to take oral contraceptives 6 months prior to the onset of the symptoms. Her parents and sisters had been asymptomatic throughout their lives, but the family history revealed a few thromboembolic accidents. Using DNA analysis, heterozygosity for factor V Leiden, prothrombin gene mutation G20210A and methylenetetrahydrofolate reductase C677T, as well as the homozygous 4G/4G genotype in the plasminogen activator inhibitor 1 were identified in our patient. Subsequently, DNA analysis was performed in all living family members, and multiple factors associated with thrombophilia were discovered. Our case confirms the multifactorial cause of thromboembolic events and emphasizes the importance of oral contraceptive use in the onset of venous thrombosis, especially in teenage females. In addition, this case indicates that teenage females with a family history of thrombosis who are making choices about contraception could most likely benefit from advanced thrombophilia testing.

V - leiden因子、凝血酶原G20210A突变、MTHFR C677T突变、PAI-1突变纯合1例17岁女孩避孕相关深静脉血栓形成及肺栓塞:多遗传危险因素家族报告及文献复习
我们提出的情况下,17岁的女孩谁突然醒来与局部疼痛在左腹股沟和无法扭转她的腿。经过全面的内科和实验室检查,确定深静脉血栓形成并随之发生肺栓塞。她最近没有任何创伤,但在症状出现前6个月开始服用口服避孕药。她的父母和姐妹在他们的生活中一直没有症状,但家族史显示一些血栓栓塞事故。通过DNA分析,我们在患者中发现了V Leiden因子、凝血酶原基因突变G20210A和亚甲基四氢叶酸还原酶C677T的杂合性,以及纤溶酶原激活物抑制剂1的4G/4G基因型纯合性。随后,对所有在世的家庭成员进行DNA分析,发现了与血栓形成相关的多种因素。我们的病例证实了血栓栓塞事件的多因素原因,并强调了口服避孕药在静脉血栓形成发病中的重要性,特别是在青少年女性中。此外,该病例表明,有血栓家族史的青少年女性在选择避孕措施时,最可能从先进的血栓检测中获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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