Wawschinek O, Beyer W
J Clin Chem Clin Biochem. 1982 Dec;20(12):929-30.
Wilson's disease, a hereditary disorder of copper metabolism, is characterized by excessive storage of this metal in several organs. Storage of copper in liver tissue is of great importance in diagnosis and therapy. By means of the combination of two methods - low-temperature ashing and flameless atomic absorption - the copper determination can be made even in smallest liver samples (needle-biopsy samples). It is therefore possible to perform a histological examination, as well as a quantitative copper determination on one puncture sample.
威尔逊氏病是一种铜代谢的遗传性疾病,其特征是这种金属在多个器官中过度蓄积。肝脏组织中铜的蓄积对诊断和治疗极为重要。通过低温灰化和无火焰原子吸收这两种方法的结合,即使是最小的肝脏样本(针吸活检样本)也能进行铜含量测定。因此,有可能对一个穿刺样本同时进行组织学检查和铜含量定量测定。