Vidra Tímea, Szomor Arpád, Battyáni István, Mühl Diana, Losonczy Hajna
Pécsi Tudományegyetem, Altalános Orvostudományi Kar, I. Belgyógyázati Klinika.
Orv Hetil. 2003 Nov 16;144(46):2283-6.
Deep venous thrombosis in the young age may be a complication of the rare congenital abnormality of the vena cava inferior. Genetic factors predisposing to thrombophilia in coincidence with vena cava malformation put the patients at much higher risk to develop thrombosis. The authors report a case of a 25-year old male who suffered from a massive deep venous thrombosis derived from the vena poplitea involving the vena iliaca communis. The molecular genetic examination of the patient revealed his combined genetic predisposition to venous thrombosis (Heterozygosity for Factor V. Leiden, Heterozygosity for prothrombin G20210A). Authors conclude that it is essential to perform all the relevant molecular genetic examinations to identify the presence of thrombophilic vulnerabilty and radiological imaging procedures in all cases of young patients with deep venous thrombosis if the suspicion of vascular malformation arises. The review of the literature revealed that the vena cava malformation in association with genetic factor predisposing to thrombophilia is an infrequent condition. In the authors knowledge this is the first report presenting a multiple combined genetic predisposition of risk factors in deep venous thrombosis.
年轻患者的深静脉血栓形成可能是下腔静脉罕见先天性异常的并发症。遗传因素导致易栓症,再加上腔静脉畸形,使患者发生血栓形成的风险大大增加。作者报告了一例25岁男性患者,其患有源于腘静脉并累及髂总静脉的大面积深静脉血栓形成。对该患者的分子遗传学检查显示其存在静脉血栓形成的联合遗传易感性(因子V莱顿杂合子、凝血酶原G20210A杂合子)。作者得出结论,如果怀疑存在血管畸形,对于所有年轻的深静脉血栓形成患者,进行所有相关的分子遗传学检查以确定是否存在易栓性以及进行放射影像学检查至关重要。文献综述显示,腔静脉畸形与遗传易栓因素相关是一种罕见情况。据作者所知,这是第一份报告呈现深静脉血栓形成中多种危险因素联合遗传易感性的病例。