Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up
<p>Abstract</p> <p>Clinical studies have confirmed that renal oncocytoma (RO) is a benign neoplasm with excellent prognosis. In diagnostically challenging cases of renal oncocytic epithelial neoplasms, fluorescent in-situ hybridization (FISH) is increasingly being used and its abil...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2010-05-01
|
Series: | Diagnostic Pathology |
Online Access: | http://www.diagnosticpathology.org/content/5/1/32 |
_version_ | 1811281748579844096 |
---|---|
author | Sherer Carol R Acquafondata Marie B Cieply Kathleen M Bastacky Sheldon I Dhir Rajiv Dvorakova Marie Mercuri Tracy L Parwani Anil V |
author_facet | Sherer Carol R Acquafondata Marie B Cieply Kathleen M Bastacky Sheldon I Dhir Rajiv Dvorakova Marie Mercuri Tracy L Parwani Anil V |
author_sort | Sherer Carol R |
collection | DOAJ |
description | <p>Abstract</p> <p>Clinical studies have confirmed that renal oncocytoma (RO) is a benign neoplasm with excellent prognosis. In diagnostically challenging cases of renal oncocytic epithelial neoplasms, fluorescent in-situ hybridization (FISH) is increasingly being used and its ability to distinguish RO from chromophobe renal cell carcinoma (ChRCC) has been documented. In this study, we evaluated the differential diagnostic contribution of FISH in cases of RO.</p> <p>Clinicopathologic data and glass slides from 73 patients with RO were reviewed; 20 cases of ChRCC were included for comparison. FISH analysis of formalin-fixed, paraffin-embedded sections was performed using centromeric probes for chromosomes 1, 2, 7 and 17. FISH analysis revealed ROs had frequent loss of signal for chromosome 1 (56%) and 17 (44%). Tumors with more than one loss were common (41%) and 10% cases showed loss of all chromosomes examined. A total of 18% cases did not show any abnormality.</p> <p>Our study shows that chromosomal abnormalities in both ROs and ChRCCs are common with frequent loss of chromosomes 1 and 17. No association was found between overall patient survival and the extent of chromosomal abnormalities. FISH results, even those showing significant chromosomal abnormalities, should not alter the primarily morphology-based diagnosis of RO.</p> |
first_indexed | 2024-04-13T01:39:11Z |
format | Article |
id | doaj.art-e74773b5f56b43b396b9d3053861d602 |
institution | Directory Open Access Journal |
issn | 1746-1596 |
language | English |
last_indexed | 2024-04-13T01:39:11Z |
publishDate | 2010-05-01 |
publisher | BMC |
record_format | Article |
series | Diagnostic Pathology |
spelling | doaj.art-e74773b5f56b43b396b9d3053861d6022022-12-22T03:08:15ZengBMCDiagnostic Pathology1746-15962010-05-01513210.1186/1746-1596-5-32Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-upSherer Carol RAcquafondata Marie BCieply Kathleen MBastacky Sheldon IDhir RajivDvorakova MarieMercuri Tracy LParwani Anil V<p>Abstract</p> <p>Clinical studies have confirmed that renal oncocytoma (RO) is a benign neoplasm with excellent prognosis. In diagnostically challenging cases of renal oncocytic epithelial neoplasms, fluorescent in-situ hybridization (FISH) is increasingly being used and its ability to distinguish RO from chromophobe renal cell carcinoma (ChRCC) has been documented. In this study, we evaluated the differential diagnostic contribution of FISH in cases of RO.</p> <p>Clinicopathologic data and glass slides from 73 patients with RO were reviewed; 20 cases of ChRCC were included for comparison. FISH analysis of formalin-fixed, paraffin-embedded sections was performed using centromeric probes for chromosomes 1, 2, 7 and 17. FISH analysis revealed ROs had frequent loss of signal for chromosome 1 (56%) and 17 (44%). Tumors with more than one loss were common (41%) and 10% cases showed loss of all chromosomes examined. A total of 18% cases did not show any abnormality.</p> <p>Our study shows that chromosomal abnormalities in both ROs and ChRCCs are common with frequent loss of chromosomes 1 and 17. No association was found between overall patient survival and the extent of chromosomal abnormalities. FISH results, even those showing significant chromosomal abnormalities, should not alter the primarily morphology-based diagnosis of RO.</p>http://www.diagnosticpathology.org/content/5/1/32 |
spellingShingle | Sherer Carol R Acquafondata Marie B Cieply Kathleen M Bastacky Sheldon I Dhir Rajiv Dvorakova Marie Mercuri Tracy L Parwani Anil V Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up Diagnostic Pathology |
title | Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up |
title_full | Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up |
title_fullStr | Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up |
title_full_unstemmed | Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up |
title_short | Renal oncocytoma: a comparative clinicopathologic study and fluorescent in-situ hybridization analysis of 73 cases with long-term follow-up |
title_sort | renal oncocytoma a comparative clinicopathologic study and fluorescent in situ hybridization analysis of 73 cases with long term follow up |
url | http://www.diagnosticpathology.org/content/5/1/32 |
work_keys_str_mv | AT sherercarolr renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT acquafondatamarieb renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT cieplykathleenm renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT bastackysheldoni renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT dhirrajiv renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT dvorakovamarie renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT mercuritracyl renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup AT parwanianilv renaloncocytomaacomparativeclinicopathologicstudyandfluorescentinsituhybridizationanalysisof73caseswithlongtermfollowup |