Ten-Year Prospective Study on the Development of Renal Cell Carcinoma in Dialysis Patients
References (44)
- et al.
Cystic kidneys: An enigma evolves
Am J Kidney Dis
(1984) - et al.
Acquired renal cystic disease in the end stage kidney: Urological implications
J Urol
(1984) Uremic acquired cystic disease of kidney
Urology
(1985)- et al.
Acquired cystic disease: Replacing one kidney disease with another
Kidney Int
(1985) - et al.
Acquired cystic disease of the end-stage kidney
Am J Med
(1985) - et al.
End stage renal disease associated with acquired cystic disease and neoplasia
J Urol
(1988) - et al.
Severity of acquired renal cysts in native kidneys and renal allograft with long-standing poor function
Am J Kidney Dis
(1989) - et al.
Neoplasms in dialysis patients: A population-based study
Am J Kidney Dis
(1989) - et al.
Renal adenocarcinoma and acquired cystic disease in chronic hemodialysis patients
Am J Kidney Dis
(1987) - et al.
Acquired cystic disease of kidney in chronic dialysis patients
Urology
(1981)
Spontaneous renal subcapsular hematoma in a patient undergoing hemodialysis
J Urol
Massive renal and retroperitoneal hemorrhage in a case of acquired renal cystic disease with atypical epithelial cell proliferation
Am J Kidney Dis
Acquired cystic disease of the kidneys: A hazard of long-term intermittent maintenance haemodialysis
J Clin Pathol
Development of acquired cystic disease and adenocarcinoma of the kidney in glomerulonephritic chronic hemodialysis patients
Clin Nephrol
Atypical cysts, acquired renal cystic disease, and renal cell tumors in end stage dialysis kidneys
Lab Invest
Acquired cystic disease and tumors in kidneys of hemodialysis patients
Isr J Med Sci
Clinical importance of acquired cystic disease of the kidney in patients undergoing dialysis
Br Med J
Multicystic transformation of kidneys in chronic renal failure
Nephron
CT of acquired cystic kidney disease and renal tumors in long-term dialysis patients
AJR
Acquired renal cystic disease and renal neoplasms in hemodialysis patients
Urol Radiol
Renal carcinoma and dialysis in end-stage renal disease
South Med J
Acquired renal cystic disease and renal adenocarcinoma in patients on long-term hemodialysis
N Engl J Med
Cited by (105)
Tumors masquerading as type 2 papillary renal cell carcinoma: pathologists’ ever-expanding differential diagnosis for a heterogeneous group of entities
2022, Urologic Oncology: Seminars and Original InvestigationsCitation Excerpt :ACD-RCC is more commonly diagnosed in men, with the average age at diagnosis in the 50s [109,110]. In general, the risk of developing RCC is much higher in patients with end-stage renal disease than in the general population [123-125], and this risk reportedly increases the longer a patient is on dialysis [126]. In contrast to most of the other entities in the differential diagnosis for PRCC, ACD-RCC is typically considered an indolent tumor, with approximately 10% of patients experiencing adverse events during clinical follow-up [110,111].
Hemodialysis Centers Guide 2020
2021, NefrologiaCancer Screening in Patients Undergoing Maintenance Dialysis: Who, What, and When
2020, American Journal of Kidney DiseasesThe De Ritis (Aspartate Transaminase/Alanine Transaminase) Ratio as a Prognosticator in Patients With End-stage Renal Disease–associated Renal Cell Carcinoma
2020, Clinical Genitourinary CancerCitation Excerpt :However, data on the prognosis of patients with ESRD-associated RCC are conflicting. Several studies indicated favorable patient survival in ESRD-associated RCC than that in sporadic RCC, whereas others indicated that the prognosis was similar between ESRD-associated and sporadic RCC.4-6 We also reported no significant difference between RCC survival in patients with ESRD and that of the general population.7
Pathologic characterization of renal epithelial neoplasms arising in nonfunctioning kidneys
2020, Human PathologyCitation Excerpt :Clinical demographics and variables, such as age, sex, dialysis history, and duration, were documented alongside pathologic parameters, such as tumor size, laterality, and uni- or multifocality. ACKD is defined as per earlier literature with the presence of at least 3 or more cysts involving a kidney with an atrophic ESRD and with no history of hereditary renal cystic disorders [11,18,19] (Fig. 1A). ACKD cysts are lined by flattened or cuboidal epithelium that may sow focal pseudopapillae with nuclear enlargement and loss of polarity (Fig. 1B).
The authors reply
2018, Kidney International