Journal Basic Info

  • Impact Factor: 1.809**
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Vascular Medicine
  •  Sleep Medicine and Disorders
  •  Family Medicine and Public Health
  •  Hepatology
  •  Gastric Cancer
  •  Signs and Symptoms-Clinical Findings
  •  Pathology
  •  Microbiology


Citation: Ann Clin Case Rep. 2016;1(1):1025.DOI: 10.25107/2474-1655.1025

Mixed Oncocytoma and Papillary Renal Cell Carcinoma

Dilek E. Baydar

Department of Pathology, Hacettepe University School of Medicine, Turkey

*Correspondance to: Dilek Ertoy Baydar 

 PDF  Full Text Case Report | Open Access


The hybrid tumors composed of oncocytoma and chromophobe renal cell carcinoma (ChRCC) are known to occur. They are seen in 3 settings, namely Birt-Hogg-Dubé Syndrome, renal oncocytosis, and as sporadic neoplasia. However, mixed renal tumors composed of a component other than ChRCC in addition to oncocytoma are extremely rare. Herein, a renal cell neoplasm consisted of two intermingled components, namely oncocytoma and papillary renal cell carcinoma were presented.


Cite the Article:

Baydar DE. Mixed Oncocytoma and Papillary Renal Cell Carcinoma. Ann Clin Case Rep. 2016; 1: 1025.

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