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Canadian Urological Association Journal logoLink to Canadian Urological Association Journal
letter
. 2015 Mar-Apr;9(3-4):88. doi: 10.5489/cuaj.2677

Papillary RCC and oncocytoma: Longer follow-up reported

Michael S Floyd Jr 1,✉, Alan R De Bolla 1
PMCID: PMC4455629  PMID: 26085863

CUAJ Letters is an open forum to discuss papers published in CUAJ. Letters are published at the discretion of the editors, and are subject to abridgement and editing for style and content. Letters can be sent to the Editor at journal@cua.org.

Dear Editor, We read with great interest the recent case report by Özer and colleagues,1 in which the very rare occurrence of a concomitant papillary renal cell carcinoma and oncocytoma is described. The article highlights the fact that oncocytomas arise from intercalated cells of the collecting ducts and that papillary carcinomas have a different cellular origin; thus the finding of these two separate tumours within a single kidney is exceptionally rare and this is the fourth case described in the literature.

Reliable radiological confirmation of oncocytomas remains difficult, as tomography is frequently unable to distinguish between malignant renal lesions and “benign” oncocytomas,2 and the definitive diagnosis is usually based on final pathological analysis. However, Cornelis and colleagues3 have explored the possibility that absence of central area signal inversion or the presence of a signal drop on chemical shift MRI may assist in ruling out oncocytomas.

We published a case of concomitant oncocytoma and papillary renal cell carcinoma in 20114 in a 73-year-old female who presented with hypercalcaemia and was successfully treated with a left partial nephrectomy. The incidental finding of hypercalcaemia may not have been due to a paraneoplastic syndrome as the patient underwent excision of a parathyroid adenoma later in 2011.

We had originally operated on this case in 2009 and in light of the recent case described we have reexamined our patient’s postoperative surveillance. We now have 5 years of follow-up with no recurrence detected (of her left renal tumour) between 2009 and 2014, with the last upper tract ultrasound performed in May 2014 – 54 months following her partial nephrectomy. The patient’s serum creatinine is normal. Therefore, although Özer and colleagues1 claim to have the longest follow-up at 18 months following concomitant oncocytoma and papillary cell carcinoma treated with radical nephrectomy, we have a similar case that remains tumour-free, based on radiological grounds, almost 5 years following partial nephrectomy.

Footnotes

Competing interests: The authors declare no competing financial or personal interests.

References

  • 1.Özer C, Gören MR, Egilmez T, et al. Papillary renal cell carcinoma within a renal oncocytoma: Case report of very rare coexistence. Can Urol Assoc J. 2014;8:E928–30. doi: 10.5489/cuaj.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Choudhary S, Rajesh A, Mayer NJ, et al. Renal oncocytoma: CT features cannot reliably distinguish oncocytoma from other renal neoplasms. Clin Radiol. 2009;64:517–22. doi: 10.1016/j.crad.2008.12.011. [DOI] [PubMed] [Google Scholar]
  • 3.Cornelis F, Lasserre AS, Tourdias T, et al. Combined late gadolinium-enhanced and double-echo chemical-shift MRI help to differentiate renal oncocytomas with high central T2 signal intensity from renal cell carcinomas. AJR Am J Roentgenol. 2013;200:830–8. doi: 10.2214/AJR.12.9122. [DOI] [PubMed] [Google Scholar]
  • 4.Floyd MS, Jr, Javed S, Pradeep KE, et al. Composite oncocytoma and papillary renal cell carcinoma of the kidney treated by partial nephrectomy: A case report. ScientificWorldJournal. 2011;11:1173–7. doi: 10.1100/tsw.2011.120. [DOI] [PMC free article] [PubMed] [Google Scholar]

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