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多囊肾病

Polycystic renal disease.

作者信息

Anderson G A, Degroot D, Lawson R K

机构信息

Department of Urology, Medical College of Wisconsin, Milwaukee.

出版信息

Urology. 1993 Oct;42(4):358-64. doi: 10.1016/0090-4295(93)90358-h.

Abstract

Renal cystic disease is a relatively common disorder whose development and progression currently appear to be due to an interaction between an abnormal basement membrane matrix, a potentially immature, hyperproliferative epithelium, and an abnormal epithelial secretory apparatus. RCC risk in cystic kidneys is the most controversial sequela of PKD. Currently, RCC risk in ESRD patients appears to be close to that present in the general population and only coincidentally associated with renal cysts. Screening of all ESRD patients for RCC and prophylactic native nephrectomy in dialysis and transplant patients does not seem to be indicated.

摘要

肾囊性疾病是一种相对常见的病症,其发生和进展目前似乎是由于异常的基底膜基质、潜在未成熟的过度增殖上皮细胞和异常的上皮分泌装置之间的相互作用所致。多囊肾患者发生肾细胞癌(RCC)的风险是最具争议的后遗症。目前,终末期肾病(ESRD)患者发生RCC的风险似乎与普通人群相近,且仅与肾囊肿偶然相关。对所有ESRD患者进行RCC筛查以及对透析和移植患者进行预防性自体肾切除术似乎并无必要。

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