Case report: Renal Cell Carcinoma (RCC) after kidney transplant (1995)

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Ready to upload
Record number: 
1542
Adverse Occurrence type: 
MPHO Type: 
Estimated frequency: 
(Council of Europe, 2022): To provide valid histological staging, complete tumour resection (R0) is required for acceptance of all organs; additionally, tumour-free margins are a prerequisite for transplant of the affected kidney. Paraffin section is superior to frozen section for the assessment of such biopsies. The contralateral kidney should always be examined for synchronous RCC (5 % of patients). RCC < 1 cm (stage T1a AJCC 8th edn) and WHO/ISUP grade I/II (Fuhrman grade I/II) can be considered minimal-risk for transmission; RCC 1-4 cm (stage T1a AJCC 8th edn) and WHO/ISUP grade I/II (Fuhrman grade I/II) are considered low-risk; RCC > 4-7 cm (stage T1b AJCC 8th edn) and WHO/ISUP grade I/II (Fuhrman grade I/II) are considered intermediate-risk; RCC > 7 cm (stage T2 AJCC 8th edn) and WHO/ISUP grade I/II (Fuhrman grade I/II) are considered high-risk; RCC with extension beyond the kidney (stages T3/T4 AJCC 8th edn) is considered a contraindication to transplant; All RCC with WHO/ISUP grade III/IV (Fuhrman grade III/IV) are considered high-risk for transmission; Contralateral kidneys and other organs that are un¬involved in carcinoma are considered to represent minimal risk for transplantation when the RCC in the involved kidney is 4 cm or less and WHO/ISUP grade I-II. In all cases, follow-up surveillance is desirable. RCC in the donor history: The transmission risk of treated RCC depends on the histological type of tumour [159] and its recurrence-free follow-up period. In general, in the first 5 years after initial diagnosis, risk categories correspond to those stated above (RCC diagnosed during donor procurement) if there is no suspicion of tumour recurrence in the donor. After this time, the risk of advanced stages may decrease.
Time to detection: 
2 years
Alerting signals, symptoms, evidence of occurrence: 
Evaluation for painless macroscopic hematuria occurring 2 years after transplantation disclosed a renal cell carcinoma which was multicentric in the kidney, invaded the renal vein and demonstrated lung metastases.
Demonstration of imputability or root cause: 
Evaluation for painless macroscopic hematuria occurring 2 years after transplantation disclosed a metastatic renal cell carcinoma, which by the use of restriction fragment length polymorphism analysis was shown to be of the donor origin.
Imputability grade: 
3 Definite/Certain/Proven
Groups audience: 
Suggest new keywords: 
metastatic disease
transplantectomy
microsatellite DNA fingerprinting
molecular analysis
Suggest references: 
Lotan, D.; Laufer, J. Metastatic renal carcinoma in a pediatric recipient of an adult cadaveric donor kidney Am J Kidney Dis 1995; 26 (6) :960 - 2
Expert comments for publication: 
Transplant nephrectomy and cessation of immunosuppression led to absence of malignancy at 1 year followup.