2021
DOI: 10.3892/mco.2021.2386
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Incidental occurrence of papillary renal cell carcinoma in the native kidney with autosomal dominant polycystic kidney disease after renal transplantation: A case report

Abstract: Autosomal dominant polycystic kidney disease (ADPKD) is one of the best-known genetic diseases. Almost half of the patients with ADPKD will develop end-stage renal disease, and the majority of patients are treated with renal transplantation. The current study presents a case that developed papillary renal cell carcinoma (PRCC) in the native right kidney 10 years after renal transplantation. PRCC is a not common malignant tumour entity (18.5% of all cases of renal cell carcinoma) compared with common clear cell… Show more

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Cited by 4 publications
(2 citation statements)
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References 36 publications
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“…However, the incidence of papillary RCC has increased among kidney transplant recipients. Some studies show that the incidence of papillary RCC after renal transplantation is up to 30% ( 8 ). The simultaneous occurrence of malignant tumors in bilateral native kidneys is rare, especially in patients without acquired cystic kidney disease.…”
Section: Literature Review and Discussionmentioning
confidence: 99%
“…However, the incidence of papillary RCC has increased among kidney transplant recipients. Some studies show that the incidence of papillary RCC after renal transplantation is up to 30% ( 8 ). The simultaneous occurrence of malignant tumors in bilateral native kidneys is rare, especially in patients without acquired cystic kidney disease.…”
Section: Literature Review and Discussionmentioning
confidence: 99%
“…12 Clear cell remains the most common histological RCC subtype, however ESRD patients and TXPs reports increased risks of papillary subtype RCC with incidence of papillary RCC after renal transplantation of up to 30%. 13…”
Section: Epidemiologymentioning
confidence: 99%