Kaur U, Bambery P, Bhushnurmath S R, Deodhar S D, Dilawari J B
Department of Experimental Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Trop Geogr Med. 1988 Apr;40(2):161-5.
We describe the clinical course of a patient with florid, predominantly neurological, Wilson's disease who developed serious toxic effects of d-penicillamine therapy but responded well to long term oral zinc sulphate. A congenital portosystemic shunt has decompressed the portal bed adequately to prevent the development of varices. We also documented the return to normal of a grossly abnormal pancreolauryl test after withdrawal of zinc.
我们描述了一位患有典型的、以神经症状为主的威尔逊氏病患者的临床病程,该患者在接受青霉胺治疗时出现了严重的毒性反应,但长期口服硫酸锌后反应良好。先天性门体分流已充分减压门静脉床,以防止静脉曲张的发生。我们还记录了停用锌后,严重异常的胰月桂基试验恢复正常的情况。