一例中年女性多发性多囊器官:罕见病例超过十年未手术治疗

Randa Zaki A M Khair, Mohamed Toum Musa M Ibrahim
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引用次数: 0

摘要

有些器官被认为比其他器官更容易出现囊肿;这些器官包括肾脏、肝脏、胰腺和脾脏。这些器官的结构和功能可能起作用。多囊肾的发生频率是可变的。据报道,10万人中有50人或更少(10000人中有5人),400人中有1人,1000人中有1人出生。常染色体显性多囊肾病(ADPKD)的患病率被认为被高估了2至5倍。多发性多囊器官并不常见,回顾文献发现一些病例报道,表明此类病例无规律性。遗传性多囊肾病有两个品种;常染色体显性多囊肾病(ADPKD)和常染色体隐性多囊肾病(ARPKD)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple Polycystic Organs in A Middle Age Female: A Rare Case of More Than Ten Years Without Surgical Intervention
Some organs are recognized to develop cysts more common than others do; these include the kidney the liver, the pancreas and the spleen. The structure and function of these organs may play a role. The frequency of polycystic kidney is variable. It is reported as 50 or less in 100000 (5 in 10000), 1 in 400 and 1 in 1000 life birth. Prevalence of autosomal dominant polycystic kidney disease (ADPKD) is thought to be overestimated by 2 to 5 folds. Multiple polycystic organs are not common, and reviewing the literature revealed some case reports, which indicates that such cases do not have regular pattern. Inherited polycystic kidney disease has two varieties; autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD).
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