论文部分内容阅读
作者复习经尸检的72例镰状细胞贫血(sickle celldisease,SCD)的病历资料。72例均根据血红蛋白电泳结果、慢性溶血性贫血史、黄疸、外周血液存有镰状红细胞而确定诊断。经血红蛋白电泳检查证实,其中35例为血红蛋白SS,12例为 SC,1例为 S-Thal。24例于血红蛋白电泳检查前,以临床标准诊断。患者年龄5个月～75岁,平均21岁。男、女各半。均为黑人。临床表现为疼痛危象15例,充血性
The authors reviewed the autopsy of 72 cases of sickle cell disease (sickle cell disease, SCD) medical records. 72 cases were based on hemoglobin electrophoresis results, history of chronic hemolytic anemia, jaundice, peripheral blood sickle red blood cells and confirm the diagnosis. Hemoglobin electrophoresis examination confirmed that 35 cases of hemoglobin SS, 12 cases of SC, 1 case of S-Thal. 24 cases of hemoglobin electrophoresis before the diagnosis of clinical standards. Patients aged 5 months to 75 years, mean 21 years old. Male and female half. All blacks. Clinical manifestations of pain crisis in 15 cases, congestive