Angel Joel R, Parker Stacey, Sells Ryan E, Atallah Ehab
Department of Medicine, Medical College of Wisconsin, Milwaukee, USA.
Blood Coagul Fibrinolysis. 2010 Jun;21(4):372-5. doi: 10.1097/mbc.0b013e32833894eb.
Klinefelter's syndrome is characterized by hypogonadism and infertility and commonly has an XXY karyotype. Within the population of men with this disorder, there is an increased incidence of venous thromboembolic disease. Although the precise mechanisms underlying this prothrombotic state have not been elucidated, it is thought that the increased incidence of thromboembolism is associated with a hypofibrinolytic state secondary to androgen deficiency. We present the case of a 26-year-old man with Klinefelter's syndrome who had recurrent episodes of deep venous thrombosis and pulmonary embolism while undergoing therapeutic anticoagulation. Coagulation studies were significant for the heterozygous mutations of MTHFR-677C>T and 1298A>C gene and hyperhomocystenemia. Our aim is to raise awareness of this association and discuss management for these patients.
克兰费尔特综合征的特征是性腺功能减退和不育,通常具有XXY核型。在患有这种疾病的男性群体中,静脉血栓栓塞性疾病的发病率增加。尽管这种促血栓形成状态的确切机制尚未阐明,但人们认为血栓栓塞发病率的增加与雄激素缺乏继发的低纤维蛋白溶解状态有关。我们报告一例26岁克兰费尔特综合征男性患者,在接受治疗性抗凝期间反复发生深静脉血栓形成和肺栓塞。凝血研究显示MTHFR - 677C>T和1298A>C基因杂合突变以及高同型半胱氨酸血症。我们的目的是提高对这种关联的认识并讨论这些患者的管理。