论文部分内容阅读
Wilson病又称肝豆状核变性,是常染色体隐性遗传疾病,近年来,提出腹型Wilson病的概念,我们遇见1例,简介如下: 患者男,8岁,因浮肿,尿少4个月入院。4个月前发热1周后,腹部浮肿,尿少,眼结膜黄染,鼻衄,某医院诊断为黄疸肝炎,治疗23天,浮肿减退出院。在家自服青霉胺、维生素B_6,半个月后腹部又逐渐肿大,鼻衄次数增多,尿少、色如浓茶入院。近来胃纳减退,大便1天3～4次。体检:神志清,面部浮肿,巩膜黄染,角膜边缘
Wilson disease, also known as hepatolenticular degeneration, is an autosomal recessive disease, in recent years, proposed the concept of abdominal Wilson disease, we met 1 case, as follows: The patient male, 8 years old, due to edema, oliguria 4 Month admission. 4 months ago fever after 1 week, abdominal edema, oliguria, conjunctival yellow dye, epistaxis, a hospital diagnosis of jaundice hepatitis, 23 days of treatment, decreased edema was discharged. At home, self-serving penicillamine, vitamin B_6, half a month later the abdomen and gradually enlarged, increased epistaxis, oliguria, color, such as strong tea hospitalization. Recently decreased appetite, stool 1 to 3 days 4 times. Physical examination: clear mind, facial edema, scleral yellow dye, corneal edge