Oncocytic papillary renal cell carcinoma: a clinicopathologic, immunohistochemical, ultrastructural, and interphase cytogenetic study of 12 cases
Language English Country United States Media print
Document type Case Reports, Journal Article
PubMed
16730306
DOI
10.1016/j.anndiagpath.2005.12.002
PII: S1092-9134(05)00209-1
Knihovny.cz E-resources
- MeSH
- Aneuploidy MeSH
- Chromosome Deletion MeSH
- Cytoplasm ultrastructure MeSH
- Diagnosis, Differential MeSH
- Adult MeSH
- In Situ Hybridization, Fluorescence MeSH
- Interphase genetics MeSH
- Carcinoma, Renal Cell chemistry genetics pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Chromosomes, Human, Pair 17 MeSH
- Chromosomes, Human, Pair 7 MeSH
- Chromosomes, Human, Y genetics MeSH
- Biomarkers, Tumor analysis MeSH
- Kidney Neoplasms chemistry genetics pathology MeSH
- Adenoma, Oxyphilic diagnosis MeSH
- Oxyphil Cells pathology MeSH
- Carcinoma, Papillary chemistry genetics pathology MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
Papillary renal cell carcinoma (RCC) is subclassified in type 1 displaying cells with scanty pale cytoplasm arranged in a single layer and in type 2 showing pseudostratified cells with eosinophilic cytoplasm. However, the existence of more variants of papillary RCC may be inferred by the recognition of few cases with different morphological features. We report the clinicopathologic, immunohistochemical, ultrastructural, and interphase cytogenetic features of 12 papillary RCC composed by oncocytes. Ten patients were males and their median age was 67 years. The tumors were well demarcated and their median diameter was 7.1 cm. Solid oncocytoma-like areas occurred in 11 cases. The cytoplasm of the neoplastic cells was filled by mitochondria with lamellar cristae. All cases were positive for the antimitochondrial antigen and racemase and showed variable immunoreactivity for cytokeratins (AE1/AE3, CK8-18, CK7, CK19), EMA, CD10, vimentin, and parvalbumin. MIB1 was detected in 0 to 6 cells per 1 high-power field. Fluorescent in situ hybridization analysis on formalin-fixed paraffin-embedded tissue showed three or more signals for chromosome 7 and 17 (for both > or =30% of nuclei in 7 of 12 neoplasms). In males, signals of chromosome Y were absent in more than 80% of the neoplastic nuclei. One patient died of metastases. Interphase cytogenetic analysis by fluorescent in situ hybridization can be a diagnostic tool in cases mimicking an oncocytoma.
References provided by Crossref.org
Molecular Genetics of Renal Cell Tumors: A Practical Diagnostic Approach
Typical signs of oncocytic papillary renal cell carcinoma in everyday clinical praxis