Goyal Sham Sunder, Bhardwaj D Vimal, Shenoy Uk, Reddy Bhavya
Department of Anaesthesiology, Kasturba Medical College, Manipal, Karnataka, India.
Indian J Anaesth. 2011 Nov;55(6):605-7. doi: 10.4103/0019-5049.90617.
Congenital afibrinogenemia is a very rare autosomal recessive disorder, results from mutation that affects plasma fibrinogen concentration. It is frequently associated with bleeding diathesis of varying severity. We describe the case of a 10-year-old child diagnosed of congenital afibrinogenemia who presented to hospital with subperiosteal haematoma and was posted for incision and drainage. Replacement therapy is the mainstay of treatment of bleeding episodes in this patient and plasma-derived fibrinogen concentrate is the agent of choice. Cryoprecipitate and fresh frozen plasma are alternative treatments. Appropriate amount of cryoprecipitate were transfused pre-operatively to the child. Individuals with congenital afibrinogenemia should be managed by a comprehensive bleeding disorder care team experienced in diagnosing and managing inherited bleeding disorders. Anaesthesiologist, surgeons and haematologist should work like a unit to manage the surgical emergencies.
先天性无纤维蛋白原血症是一种非常罕见的常染色体隐性疾病,由影响血浆纤维蛋白原浓度的突变引起。它常伴有不同严重程度的出血倾向。我们描述了一例10岁被诊断为先天性无纤维蛋白原血症的儿童病例,该患儿因骨膜下血肿入院并计划接受切开引流术。替代疗法是该患者出血发作治疗的主要方法,血浆源性纤维蛋白原浓缩物是首选药物。冷沉淀和新鲜冰冻血浆是替代治疗方法。术前给该患儿输注了适量的冷沉淀。先天性无纤维蛋白原血症患者应由一个在诊断和管理遗传性出血性疾病方面经验丰富的综合出血性疾病护理团队进行管理。麻醉医生、外科医生和血液科医生应像一个团队一样协作来处理手术急症。