论文部分内容阅读
遗传性椭圆形红细胞增多症,是一种较罕见的遗传性血液病。现将我们见到的1例及其家族调查结果报告如下:患者女,34岁,小学教师。5个月来全身无力、食欲减退头晕、腹张。3个月前做人工流产后,发现面部苍白,巩膜发黄,面部及双下肢浮肿,曾于当地医院检查,可疑“溶血性贫血”,口服肝铁糖片、VB_(12)治疗,食欲渐好,浮肿消退。后又来我院就诊。患者15岁时,每于过劳后,先巩膜发黄,后全身皮肤发黄,恶心(?)呕吐。每于感冒后尿黄,不治疗能自行缓解,10多年来发作20余次。26岁结婚,生育两胎,男孩9岁,女孩7岁均健在。
Hereditary oval polycythemia, is a rare hereditary hematological disease. Now we see 1 case and its family findings are reported as follows: Female patient, 34 years old, primary school teacher. 5 months to the general weakness, loss of appetite, dizziness, abdominal. 3 months ago after an abortion, pale, sclera yellow, facial and lower extremity edema, had a local hospital examination, suspected “hemolytic anemia”, oral hepatic iron tablets, VB_ (12) treatment, loss of appetite Well, edema subsided. Later came to our hospital. At 15 years of age, the sclera was yellowed and the entire body was yellowed and nauseated (?) Vomited after overwork. After every cold, urine yellow, no treatment can relieve itself, more than 20 attacks in 10 years. 26-year-old married, two children, 9-year-old boy, 7-year-old girl are alive.