Definition
A proposed distinct variant of papillary renal cell carcinoma with an extensively papillary architecture and oncocytic cells.
All ten reported patients were male with a median age of 71 years.
Tumours were intrarenal and well demarcated (pT1N0).
The tumour forms thin papillae with a thin fibrous core lined by a single layer of oncocytic cells having deeply eosinophilic finely granular cytoplasm. Nuclei are round with central nucleoli. The cores of the papillae contain numerous lipophages. Haemorrhage and necrosis are common. The mitotic rate is low. Hale's colloidal iron stain is negative.
Antimitochondrial antibody |
10/101 |
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10/101 |
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10/101 |
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10/101 |
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5/101 |
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4/101 |
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3/101 |
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2/101 |
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1/101 |
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1/101 |
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0/101 |
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Oncocytoma: lacks a papillary architecture or necrosis.
Papillary carcinoma: the cells are not oncocytic. Type II tumours have eosinophilic cytoplasm but differ in showing high grade cytology. There is characteristically trisomy of chromosome 17.
All patients were tumour free at a median of five years after radical nephrectomy.
©SMUHT/PW Bishop