Armean Iulia, Meliț Lorena Elena, Simu Iunius, Duicu Carmen
Emergency Clinical County Hospital Tîrgu Mureș, Pediatrics Clinic No. 1, Tîrgu Mureş, Romania.
University of Medicine and Pharmacy Tîrgu Mureș, 1st Department of Pediatrics, Tîrgu Mureş, Romania.
J Crit Care Med (Targu Mures). 2018 Jul 1;4(3):101-104. doi: 10.2478/jccm-2018-0015. eCollection 2018 Jul.
Thrombophilia represents a tendency towards excessive blood clotting and the subsequent development of venous thromboembolism (VTE). VTE is a rare condition in children that comprises both deep venous thrombosis (DVT) and pulmonary embolism (PE). This paper reports the case of a 16-year-old girl, admitted to the Pediatrics Clinic No. 1, Tîrgu Mureș, Romania, for dyspnea, chest pain and loss of consciousness. Her personal history showed that she had had two orthopedic surgical interventions in infancy, two pregnancies, one spontaneous miscarriage and a recent caesarian section at 20 weeks of gestation for premature detachment of a normally positioned placenta associated with a deceased fetus. Laboratory tests showed increased levels of D-dimers. Angio-Computed Tomography (Angio-CT) showed multiple filling defects in both pulmonary arteries, establishing the diagnosis of PE. The laboratory tests were undertaken to assist in the diagnoses of a possible thrombophilia underlined a low level of antithrombin III. Antiphospholipid syndrome was ruled out and genetic tests revealed no specific mutation. Anticoagulant therapy was initiated with unfractionated heparin and afterwards subcutaneously low molecular heparin was prescribed for three months. Later it has been changed to oral therapy with acenocoumarol. The patient was discharged in good general status with the recommendation of life-long anticoagulation therapy. Thrombophilia is a significant risk factor for PE, and it must be ruled out in all cases of repeated miscarriage.
易栓症表现为血液过度凝结及随后发生静脉血栓栓塞(VTE)的倾向。VTE在儿童中是一种罕见病症,包括深静脉血栓形成(DVT)和肺栓塞(PE)。本文报告了一名16岁女孩的病例,她因呼吸困难、胸痛和意识丧失入住罗马尼亚特尔古穆列什第一儿科诊所。她的个人病史显示,她在婴儿期接受过两次骨科手术,经历过两次怀孕、一次自然流产,最近在妊娠20周时因正常位置的胎盘早剥伴死胎而进行了剖宫产。实验室检查显示D-二聚体水平升高。血管计算机断层扫描(Angio-CT)显示双肺动脉多处充盈缺损,确诊为PE。为协助诊断可能的易栓症而进行的实验室检查显示抗凝血酶III水平较低。排除了抗磷脂综合征,基因检测未发现特定突变。开始使用普通肝素进行抗凝治疗,之后皮下注射低分子肝素三个月。后来改为口服醋硝香豆素治疗。患者出院时一般状况良好,并被建议进行终身抗凝治疗。易栓症是PE的一个重要危险因素,在所有反复流产的病例中都必须排除。