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常染色体显性多囊肾病患者的肝囊肿

Liver cysts in patients with autosomal dominant polycystic kidney disease.

作者信息

Milutinovic J, Fialkow P J, Rudd T G, Agodoa L Y, Phillips L A, Bryant J I

出版信息

Am J Med. 1980 May;68(5):741-4. doi: 10.1016/0002-9343(80)90266-1.

Abstract

Liver cysts were found in 46 (29 per cent) of 158 patients over 10 years of age with documented autosomal dominant-type polycystic kidney disease (PKD) from 62 unrelated families. Hepatic cysts were not found in any patient at risk for PKD in whom renal cysts were not detected. The prevalence of liver cysts increased with advancing age and with declining rate of glomerular filtration. Results of clinical and laboratory studies indicate that polycystic liver disease in patients with autosomal dominant-type PKD is a benign condition, rarely, if ever, causing impaired liver function or portal hypertension.

摘要

在对来自62个无亲缘关系家庭的158例10岁以上、确诊为常染色体显性多囊肾病(PKD)的患者进行研究时,发现其中46例(29%)存在肝囊肿。在任何有PKD风险但未检测到肾囊肿的患者中均未发现肝囊肿。肝囊肿的患病率随年龄增长和肾小球滤过率下降而增加。临床和实验室研究结果表明,常染色体显性PKD患者的多囊肝病是一种良性疾病,极少导致肝功能损害或门静脉高压。

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