耳源性窦血栓形成与血友病1例临床分析

I. Veshkurtseva, A. Izvin, N. Kuznetsova, S. A. Kudymov, A. Y. Sinyakov, T. Kuznetsova
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引用次数: 0

摘要

背景血友病患者由于缺乏一种凝血因子而免于血栓形成,因此血栓并发症在他们中很少见。目前,文献中很少有关于成人血友病患者自发性静脉血栓形成的描述。儿科实践中报告的血栓栓塞并发症的数据更少。目前,还没有明确的建议来治疗血友病儿童的血栓性并发症,这需要对这个问题进行进一步的研究,以制定预防和治疗方案,包括这类患者的耳源性窦血栓形成。案例描述。一名7岁男孩从躯体医院被转移到秋明(俄罗斯)第二地区临床医院的重症监护室,该医院设有耳鼻喉科。他被诊断为非穿孔型急性右侧化脓性中耳炎、急性右侧乳突炎、右乙状窦血栓形成。记忆显示,该儿童被诊断为中度血友病A(因子VIII水平为5%),去年他一直在接受因子VIII替代治疗。入院后,全身血液检查显示没有异常,急性期参数略有增加:C反应蛋白、纤维蛋白原、低凝迹象。由于消极的动力,孩子在强化替代治疗的背景下接受了乳突切除术。手术显示胃窦和胃窦有肉芽组织伴出血性血栓。在术后期间,置换治疗伴有抗菌和抗凝治疗。结论在遗传性因子VIII缺乏的背景下,耳源性鼻窦血栓形成患者的治疗是一项艰巨的任务。一方面,它需要手术干预和抗凝治疗以防止进一步的血栓形成,另一方面,需要强化替代治疗以降低出血并发症的风险。所描述的病例表明,需要一种跨学科的方法来诊断和治疗以血友病a为背景的耳源性侧窦血栓形成患者。该方法是将术中并发症的风险降至最低,并确保良好的结果。
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Otogenic Sinus Thrombosis and Hemophilia: A Clinical Case
Background. Patients with hemophilia are protected from thrombosis by a deficiency of one of coagulation factors, therefore thrombotic complications are rare in them. Currently, few descriptions of spontaneous venous thrombosis in adult hemophiliacs can be found in the literature. Even fewer data of thromboembolic complications are reported in pediatric practice. At present, no clear recommendations are given for the management of thrombotic complications in children with hemophilia, which requires further study of this issue to develop prevention and treatment regimens, including otogenic sinus thrombosis in this category of patients.Case description. A 7-year-old boy was transferred from the Somatic Hospital to the Intensive Care Unit of Regional Clinical Hospital No. 2 in Tyumen (Russia) with an Otorhinolaryngology Unit. He was diagnosed with non-perforative form of acute right-sided suppurative otitis media, acute right-sided mastoiditis, thrombosis of the right sigmoid sinus. The anamnesis shows that the child is diagnosed with hemophilia A, of moderate severity (factor VIII level — 5%), for which he has been receiving factor VIII replacement therapy for the last year. Upon admission, a general blood test revealed no abnormalities, with a slight increase in acute-phase parameters: C-reactive protein, fibrinogen, signs of hypocoagulation. Due to negative dynamics, the child underwent anthromastoidotomy against the background of intensive replacement therapy. Surgery revealed the presence of granulation tissue with hemorrhagic thrombi in the antrum and aditus. In the postoperative period, replacement therapy was accompanied with antibacterial and anticoagulant therapy.Conclusion. The management of patients with otogenic sinus thrombosis against the background of hereditary factor VIII deficiency is a difficult task. On the one hand, it requires surgical intervention and anticoagulant therapy in order to prevent further thrombosis, on the other hand — intensive replacement therapy in order to reduce the risks of hemorrhagic complications. The described case demonstrates the need for an interdisciplinary approach to the diagnosis and treatment of a patient with otogenic thrombosis of lateral sinus against the background of hemophilia A. The approach is to minimize the risks of intraoperative complications and insure a favorable outcome.
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