Douvas Michael Gregory, Monahan Paul Edward
Department of Pediatrics, University of North Carolina at Chapel Hill School of Medicine, USA.
J Pediatr Hematol Oncol. 2004 Apr;26(4):258-63. doi: 10.1097/00043426-200404000-00010.
The authors report the case of a neonate presenting with a distended abdomen and shock from factor IX (F.IX) deficiency and intrahepatic bleeding. After resuscitation and treatment with recombinant F.IX through a central venous line, he developed superior vena cava, upper extremity, and intracerebral venous thrombosis resulting in superior vena cava syndrome and intrathalamic hemorrhage. He was treated with F.IX to achieve near-normal F.IX activity levels and with low-dose unfractionated heparin with clinical improvement. F.IX replacement on a subsequent admission was again complicated by upper venous system thrombosis and improved with low-dose heparin. The case illustrates an unusual presentation of hemophilia, life-threatening thrombotic complications associated with factor replacement, and a strategy for anticoagulant management in the setting of hemophilic bleeding.
作者报告了一例新生儿病例,该患儿因缺乏凝血因子IX(F.IX)及肝内出血出现腹部膨隆和休克。经中心静脉导管给予重组F.IX进行复苏和治疗后,他发生了上腔静脉、上肢及脑内静脉血栓形成,导致上腔静脉综合征和丘脑内出血。给予F.IX治疗使F.IX活性水平接近正常,并给予小剂量普通肝素治疗,临床症状有所改善。在随后的一次入院治疗中,F.IX替代治疗再次并发上静脉系统血栓形成,经小剂量肝素治疗后病情好转。该病例说明了血友病的一种不寻常表现、与因子替代相关的危及生命的血栓并发症,以及血友病出血情况下的抗凝管理策略。