摘要
目的 :为探讨外科治疗家族性淀粉样多神经变 (Familialamyloidpolyneuropathy ,FAP)的疗效。方法 :对一FAP患者实施了背驮式肝移植。结果 :手术顺利 ,术后 1周感觉运动神经及植物神经紊乱综合症开始恢复 ,失明的双眼开始感光。术后 35d ,多神经变综合症不同程度改善后出院。初步随诊 3月 ,病情正处康复阶段。结论
Objective:To discuss the surgical therapy of familial amyloid polyneuropathy (FAP).Methods: One case of FAP was treated with piggyback liver transplantation.Results:The operation was smooth without events, and the patient's sensational, motive and vegetative nervous syndromes began to improve one week after operation, and both his blind eyes began to have light sense. The patient was discharged 35 days after operation when his polyneuropathy syndromes improved with different degrees. He has been followed up for 3 months and he is still in convalescence.Conclusions:FAP is a hereditary disorder with common chromosomal dominance which has no medicine therapy, and it can only be treated with piggyback liver transplantation. The mechanism, diagnosis of FAP, and timing and the surgical curative effect of the operation were discussed due to their inadequate common knowledge.
出处
《中国现代医学杂志》
CAS
CSCD
2002年第8期1-2,9,共3页
China Journal of Modern Medicine