论文部分内容阅读
随着先进的影像诊断仪的临床应用,无症状的小儿先天性肝囊肿(CHC)已不再是少见病。自1992年6月至1995年10月,我们诊治小儿CHC8例,现报告如下。 资料与结果 一、临床资料 男性6例,女性2例;年龄6~14岁,平均9.8岁;6例系上感发热检查中发现,2例体检发现;8例均行B超检查,提示无回声暗区,囊肿直径4~8cm,均位于右叶,单发6例,多发2例,其中1例伴左肾囊肿;2例CT检查,增强造影后未见囊肿填充;8例包虫囊液皮内试验阴性,并经囊
With the clinical application of advanced imaging diagnostic apparatus, asymptomatic pediatric congenital hepatic cysts (CHC) are no longer rare. From June 1992 to October 1995, we diagnosed 8 cases of pediatric CHC, are as follows. Data and results A clinical data of 6 males and 2 females; aged 6 to 14 years, mean 9.8 years old; 6 cases of upper exothermic examination found that 2 cases of physical examination found; 8 cases underwent B-ultrasound, suggesting no Echo dark area, the cyst diameter 4 ~ 8cm, are located in the right lobe, single in 6 cases, 2 cases of multiple, including 1 case with left renal cyst; 2 cases of CT examination, enhanced cyst filling after enhancement; 8 cases of hydatid Liquid intradermal test negative, and the capsule