第Ⅷ、第Ⅸ因子合并缺乏血友病,报告甚少,我院最近收治一例,报告如下:何××,男,19岁。于1979年6月7日因两天前口唇外伤出血不止而入院。患者6年前初次出现齿龈自发性出血,量少,此后不断反复出血。平时稍受创伤后皮肤就呈大片瘀斑,但几天后即可自行吸收。右膝和左踝关节经常外伤后肿胀,活动受限,不能伸展和弯曲。6年来,上述症状反复出现。入院前两天,因骑车不慎而跌裂口唇,流血不止,失血约400多毫升,经外科局部缝合、输鲜血等抢救方逐渐停止。患者家族中也有类似出血病例,其姨表弟幼年因外伤后出血死亡,患者舅舅在我院多次住院确诊为血 The Ⅷ, Ⅸ factors combined lack of hemophilia, the report few, our hospital recently admitted a case, the report is as follows: He XX, male, 19 years old. On June 7, 1979, she was hospitalized for bleeding more than two days ago on the lips. Patient spontaneous bleeding gums for the first time 6 years ago, a small amount, and then repeated repeated bleeding. Slightly trauma after the skin was generally large ecchymosis, but a few days after the self-absorption. Right knee and left ankle often swelling after trauma, limited mobility, can not stretch and bend. Over the past 6 years, the above symptoms recur. Two days before admission, due to cycling accidentally broken lips, bleeding more than about 400 ml of blood loss, the surgical partial suture, blood and other rescue parties gradually stopped. There are also similar cases of patients with bleeding cases, his younger brother cousin died of traumatic bleeding, the patient uncle hospitalized many times in our hospital diagnosed with blood