Lu Yi, Wang Xiao-hong, Wang Jian-she
Children's Hospital of Fudan University, Shanghai, China.
Zhonghua Gan Zang Bing Za Zhi. 2008 Mar;16(3):224-6.
To review the clinical features and liver pathology in children with hepatolenticular degeneration.
Clinical manifestations and results of lab tests and liver biopsies of 97 cases diagnosed as hepatolenticular degeneration in Children's Hospital of Fudan University from Jan 1990 to Nov 2006 were reviewed.
Manifestations of liver malfunction were the most common reason (74%) for their clinic visits. All cases showed liver involvement and nervous system involvement was found in 45%. Positive K-F rings were detected in 63 of 95 cases; ceruloplasmin level was low in 91 of the 94 cases, and 24 hour urinary copper excretion exceeded 100 microg in 25 out of 37 cases who had had this test. Seventeen cases had a liver biopsy. Various levels of inflammation and fibrosis were noted in all 17 biopsies; 8 of the 17 also had steatosis and 3 of the 17 also had glycogen accumulation.
Liver abnormality is a consistent feature in children with hepatolenticular degeneration. Corneal K-F rings, serum ceruloplasmin and the 24-hour urinary copper test have limited values for an early diagnosis of the disease. Liver pathology can be a reference in the diagnosis of hepatolenticular degeneration.
回顾肝豆状核变性患儿的临床特征及肝脏病理表现。
对1990年1月至2006年11月在复旦大学附属儿科医院确诊为肝豆状核变性的97例患儿的临床表现、实验室检查结果及肝脏活检情况进行回顾性分析。
肝功能异常是患儿就诊最常见的原因(74%)。所有病例均有肝脏受累,45%有神经系统受累。95例中有63例检测到阳性K-F环;94例中有91例血清铜蓝蛋白水平降低,37例行24小时尿铜排泄检测的病例中有25例超过100μg。17例行肝脏活检。17例活检均可见不同程度的炎症和纤维化;17例中有8例有脂肪变性,17例中有3例有糖原蓄积。
肝脏异常是肝豆状核变性患儿的一个持续特征。角膜K-F环、血清铜蓝蛋白及24小时尿铜检测对该病的早期诊断价值有限。肝脏病理可作为肝豆状核变性诊断的参考。