Bhatty Tan, Moazin Ms, Haque R
Division of Urology, Department of Surgical Specialities, King Fahad Medical City, Riyadh, Saudi Arabia.
Ecancermedicalscience. 2012;6:267. doi: 10.3332/ecancer.2012.267. Epub 2012 Sep 4.
We present a case of huge bilateral polycystic kidneys, with suspicion of malignancy and repeated admissions with acute abdomen, secondary to bleeding in cysts, and anaemia, requiring affected side nephrectomy.
Autosomal dominant polycystic kidney disease (ADPKD) mostly ends up with end stage renal disease (ESRD), requiring haemodialysis, with increased risk of malignancy and enlargement of kidneys with its associated complications, mostly dealt with conservatively, except malignancy, which requires nephrectomy.
我们报告一例巨大双侧多囊肾病例,怀疑有恶变,因囊肿出血继发急腹症和贫血而反复入院,最终进行了患侧肾切除术。
常染色体显性多囊肾病(ADPKD)大多最终发展为终末期肾病(ESRD),需要进行血液透析,恶变风险增加,肾脏增大及其相关并发症大多采用保守治疗,恶变情况除外,恶变需要进行肾切除术。