a型血友病患者在Hartmann手术后取口合并FVIII抑制剂的产生(回顾与病例报告)

S. V. Shtyrkova, S. Shutov, P. A. Batrov, E. Rybakov, N. V. Prasolov
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引用次数: 0

摘要

血友病A的具体表现之一是自发的腹部血肿,模仿急性腹部疾病的临床表现。FVIII自身抗体的出现导致对替代止血治疗的反应丧失,需要个体化治疗和高度敏感的实验室监测,以减少出血失控的风险。本文介绍了多阶段手术治疗该并发症的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stoma takedown after Hartmann’s procedure in a patient with hemophilia A complicated with production of inhibitor to FVIII (review and case report)
One of the specific manifestations of hemophilia A is the spontaneous abdominal hematoma mimicking the clinical picture of acute abdominal disease. The appearance of auto-antibodies to FVIII leads to a loss of response to replacement hemostatic therapy and requires an individualized approach as well as highly sensitive laboratory monitoring to reduce the risk of uncontrolled bleeding. The paper presents the case of multi-stage surgical treatment of this complication.
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