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常染色体显性多囊肾病中的肝囊肿

Hepatic cysts in autosomal dominant polycystic kidney disease.

作者信息

Everson G T

机构信息

Gastroenterology Division, University of Colorado Health Sciences Center, Denver.

出版信息

Mayo Clin Proc. 1990 Jul;65(7):1020-5. doi: 10.1016/s0025-6196(12)65165-9.

Abstract

Hepatic cysts are one of several extrarenal manifestations of the ADPKD gene. Several factors, including age, gender, pregnancy, the degree of renal cystic disease, and the extent of renal functional impairment, may modify the expression of hepatic cystic disease. With advances in medical care, such as improvement in the management of end-stage renal disease, hemodialysis, and renal transplantation, patients with ADPKD will experience an increased life expectancy. As a result, complications associated with hepatic cysts may become more common, and physicians may encounter an increasing number of patients with ADPKD who have infected hepatic cysts. Several issues in the management of this complication remain unresolved, but the article by Telenti and associates in this issue of the Proceedings addresses some of the critical issues that physicians who are responsible for the care of these patients will certainly confront in future years.

摘要

肝囊肿是常染色体显性多囊肾病(ADPKD)基因的几种肾外表现之一。包括年龄、性别、妊娠、肾囊性疾病程度以及肾功能损害程度在内的多种因素,可能会改变肝囊性疾病的表现。随着医疗护理的进步,如终末期肾病管理、血液透析和肾移植的改善,ADPKD患者的预期寿命将会延长。因此,与肝囊肿相关的并发症可能会变得更加常见,医生可能会遇到越来越多患有感染性肝囊肿的ADPKD患者。这种并发症管理中的几个问题仍未得到解决,但特伦蒂及其同事在本期《会议论文集》中的文章探讨了一些关键问题,负责照料这些患者的医生在未来几年肯定会面临这些问题。

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