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Sub-typing of renal cell tumours; contribution of ancillary techniques 英文参考文献
Diagnostic Pathology
BioMedCentral
Short report
Open Access
Sub-typing of renal cell tumours; contribution of ancillary
techniques
Dinesh Pradhan?1, Nandita Kakkar?1, Amanjit Bal?1, Shrawan Kumar Singh?2
and Kusum Joshi*1
Address: 1Department of Histopathology, Post Graduate Institute of Medical Sciences Research, (PGIMER), Chandigarh, India and 2Advanced
Urology Centre, Post Graduate Institute of Medical Sciences Research, (PGIMER), Chandigarh, India
Email: Dinesh Pradhan - dppgi4u@; Nandita Kakkar - nandita_kakkar@; Amanjit Bal - docaman5@;
Shrawan Kumar Singh - pgimer@chd.nic.in; Kusum Joshi* - kus_joshi@
* Corresponding author ?Equal contributors
Published: 28 June 2009
Received: 12 May 2009
Accepted: 28 June 2009
Diagnostic Pathology 2009, 4:21
doi:10.1186/1746-1596-4-21
This article is available from: /content/4/1/21
? 2009 Pradhan et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background: Adult renal epithelial neoplasms are a heterogeneous group with varying prognosis
and outcome requiring sub-classification.
Methods: Cases of renal cell carcinoma (RCC) in a 10 years period were analyzed with regard to
the clinical features and histology. Sections were reviewed by four pathologists and the discordant
cases were resolved with the help of Hales colloidal iron stain, vimentin, CK 7, and vinculin
immunostains and electron microscopy.
Results: Amongst the total of 278 cases, clear cell renal cell carcinoma was the commonest tumor
with 74.8% cases, followed by papillary RCC 12.2%, chromophobe RCC 7.9%, oncocytoma 1.8%,
and one case of collecting duct RCC. Eight cases were of sarcomatoid renal cell carcinoma. In 28/
278 cases, diagnoses varied amongst the four pathologists and the
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