“…Some have advocated prophylactic bilateral nephrectomies [3,9] on the basis of difficulty in preoperative diagnosis and that it may be a premalignant condition [11]. Others have preferred a unilateral nephrectomy because of the obvious disadvantages of bilateral nephrectomies [12]. Hence only the diseased kidney harboring malignancy should be nephrectomized, and utmost attention and follow-up are warranted for the remaining renal unit with all available appropriate investigative modalities.…”
Section: Discussionmentioning
confidence: 99%
“…Urol Int 2000;64: [9][10][11][12] Hemal/Khaitan/Singh/Kumar 3). On long-term follow-up of 2 years none of the patients developed contralateral tumors or distant metastases, except for 1 who had a recurrence in the renal fossa.…”
Renal cell carcinoma in adult polycystic kidney disease is of rare occurrence and poses a diagnostic and therapeutic challenge. We have treated three such patients in our department. One was male and two were females ranging in age from 20 to 60 years. All were diagnosed preoperatively with ultrasonography or contrast-enhanced CT. Radical nephrectomy was performed in all patients. During the follow-up no patient had recurrence in the contralateral kidney. One patient had local recurrence in the renal fossa and was treated with local radiotherapy and immunotherapy. In the past due to difficulty in diagnosis, invasive investigations like angiography were recommended and prophylactic contralateral nephrectomy was often undertaken. With the availability of reliable noninvasive investigations these patients can be diagnosed accurately and the contralateral kidney saved in most cases.
“…Some have advocated prophylactic bilateral nephrectomies [3,9] on the basis of difficulty in preoperative diagnosis and that it may be a premalignant condition [11]. Others have preferred a unilateral nephrectomy because of the obvious disadvantages of bilateral nephrectomies [12]. Hence only the diseased kidney harboring malignancy should be nephrectomized, and utmost attention and follow-up are warranted for the remaining renal unit with all available appropriate investigative modalities.…”
Section: Discussionmentioning
confidence: 99%
“…Urol Int 2000;64: [9][10][11][12] Hemal/Khaitan/Singh/Kumar 3). On long-term follow-up of 2 years none of the patients developed contralateral tumors or distant metastases, except for 1 who had a recurrence in the renal fossa.…”
Renal cell carcinoma in adult polycystic kidney disease is of rare occurrence and poses a diagnostic and therapeutic challenge. We have treated three such patients in our department. One was male and two were females ranging in age from 20 to 60 years. All were diagnosed preoperatively with ultrasonography or contrast-enhanced CT. Radical nephrectomy was performed in all patients. During the follow-up no patient had recurrence in the contralateral kidney. One patient had local recurrence in the renal fossa and was treated with local radiotherapy and immunotherapy. In the past due to difficulty in diagnosis, invasive investigations like angiography were recommended and prophylactic contralateral nephrectomy was often undertaken. With the availability of reliable noninvasive investigations these patients can be diagnosed accurately and the contralateral kidney saved in most cases.
“…The prevalence of ACKD is 190% in patients on longterm hemodialysis [4]. A comprehensive review of ACKD in ESRD found an overall radiologic imaging prevalence rate of 35% and an autopsy/nephrectomy prevalence rate of 41% [12].…”
Section: Discussionmentioning
confidence: 99%
“…The reported incidence of renal tumors (adenomas and carcinomas) in patients with ACKD is variable, depending on the definition of ACKD, method of detection (ul- [7,12,22]. Most studies have demonstrated that renal cancer occurs in 6-20% of patients with ACKD [4,17].…”
Section: Association Of Ackd With Renal Tumorsmentioning
Two patients treated with chronic dialysis and renal transplantation developed acute hemorrhage from a native kidney. Bilateral native nephrectomy demonstrated acquired cystic disease and adenocarcinoma in each of the four kidneys. The etiology of acquired cystic kidney disease (ACKD) is unclear and its incidence increases with the duration of dialysis. ACKD patients have a propensity to develop adenomas and adenocarcinomas. The increased incidence of renal neoplasms in ACKD patients warrants careful radiologic monitoring of native end-stage kidneys in selected patients.
“…ACDK has been defined as macroscopic cystic structures compromising at least 25% of the renal parenchyma or greater than 3 cysts per kidney in a patient in renal failure who was not known to have cysts prior to the onset of renal failure and in whom there is no family history or other evidence of an inherited cystic disease 1 . Of patients on dialysis for less than 3 years 10% to have ACDK, 40% to 60% on dialysis for 3 years have ACDK and more than 90% have ACDK after 5 years on dialysis 24 . The current study also demonstrated that duration of dialysis was closely related with development of ACDK.…”
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