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Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography
BACKGROUND: Full-field optical coherence tomography (FFOCT) is a real-time imaging technique that rapidly generates images reminiscent of histology without any tissue processing, warranting its exploration for evaluation of ex vivo kidney tissue. METHODS: Fresh tissue sections from tumor and adjacen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629311/ https://www.ncbi.nlm.nih.gov/pubmed/26605118 http://dx.doi.org/10.4103/2153-3539.166014 |
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author | Jain, Manu Robinson, Brian D. Salamoon, Bekheit Thouvenin, Olivier Boccara, Claude Mukherjee, Sushmita |
author_facet | Jain, Manu Robinson, Brian D. Salamoon, Bekheit Thouvenin, Olivier Boccara, Claude Mukherjee, Sushmita |
author_sort | Jain, Manu |
collection | PubMed |
description | BACKGROUND: Full-field optical coherence tomography (FFOCT) is a real-time imaging technique that rapidly generates images reminiscent of histology without any tissue processing, warranting its exploration for evaluation of ex vivo kidney tissue. METHODS: Fresh tissue sections from tumor and adjacent nonneoplastic kidney (n = 25 nephrectomy specimens; clear cell renal cell carcinoma (CCRCC) = 12, papillary RCC (PRCC) = 4, chromophobe RCC (ChRCC) = 4, papillary urothelial carcinoma (PUC) = 1, angiomyolipoma (AML) = 2 and cystic nephroma = 2) were imaged with a commercial FFOCT device. Sections were submitted for routine histopathological diagnosis. RESULTS: Glomeruli, tubules, interstitium, and blood vessels were identified in nonneoplastic tissue. In tumor sections, the normal architecture was completely replaced by either sheets of cells/trabeculae or papillary structures. The former pattern was seen predominantly in CCRCC/ChRCC and the latter in PRCC/PUC (as confirmed on H&E). Although the cellular details were not very prominent at this resolution, we could identify unique cytoplasmic signatures in some kidney tumors. For example, the hyper-intense punctate signal in the cytoplasm of CRCC represents glycogen/lipid, large cells with abundant hyper-intense cytoplasm representing histiocytes in PRCC, and signal-void large polygonal cell representing adipocytes in AML. According to a blinded analysis was performed by an uropathologist, all nonneoplastic tissues were differentiated from neoplastic tissues. Further, all benign tumors were called benign and malignant were called malignant. A diagnostic accuracy of 80% was obtained in subtyping the tumors. CONCLUSION: The ability of FFOCT to reliably differentiate nonneoplastic from neoplastic tissue and identify some tumor types makes it a valuable tool for rapid evaluation of ex vivo kidney tissue e.g. for intraoperative margin assessment and kidney biopsy adequacy. Recently, higher resolution images were achieved using an experimental FFOCT setup. This setup has the potential to further increase the diagnostic accuracy of FFOCT. |
format | Online Article Text |
id | pubmed-4629311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46293112015-11-24 Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography Jain, Manu Robinson, Brian D. Salamoon, Bekheit Thouvenin, Olivier Boccara, Claude Mukherjee, Sushmita J Pathol Inform Original Article BACKGROUND: Full-field optical coherence tomography (FFOCT) is a real-time imaging technique that rapidly generates images reminiscent of histology without any tissue processing, warranting its exploration for evaluation of ex vivo kidney tissue. METHODS: Fresh tissue sections from tumor and adjacent nonneoplastic kidney (n = 25 nephrectomy specimens; clear cell renal cell carcinoma (CCRCC) = 12, papillary RCC (PRCC) = 4, chromophobe RCC (ChRCC) = 4, papillary urothelial carcinoma (PUC) = 1, angiomyolipoma (AML) = 2 and cystic nephroma = 2) were imaged with a commercial FFOCT device. Sections were submitted for routine histopathological diagnosis. RESULTS: Glomeruli, tubules, interstitium, and blood vessels were identified in nonneoplastic tissue. In tumor sections, the normal architecture was completely replaced by either sheets of cells/trabeculae or papillary structures. The former pattern was seen predominantly in CCRCC/ChRCC and the latter in PRCC/PUC (as confirmed on H&E). Although the cellular details were not very prominent at this resolution, we could identify unique cytoplasmic signatures in some kidney tumors. For example, the hyper-intense punctate signal in the cytoplasm of CRCC represents glycogen/lipid, large cells with abundant hyper-intense cytoplasm representing histiocytes in PRCC, and signal-void large polygonal cell representing adipocytes in AML. According to a blinded analysis was performed by an uropathologist, all nonneoplastic tissues were differentiated from neoplastic tissues. Further, all benign tumors were called benign and malignant were called malignant. A diagnostic accuracy of 80% was obtained in subtyping the tumors. CONCLUSION: The ability of FFOCT to reliably differentiate nonneoplastic from neoplastic tissue and identify some tumor types makes it a valuable tool for rapid evaluation of ex vivo kidney tissue e.g. for intraoperative margin assessment and kidney biopsy adequacy. Recently, higher resolution images were achieved using an experimental FFOCT setup. This setup has the potential to further increase the diagnostic accuracy of FFOCT. Medknow Publications & Media Pvt Ltd 2015-09-28 /pmc/articles/PMC4629311/ /pubmed/26605118 http://dx.doi.org/10.4103/2153-3539.166014 Text en Copyright: © 2015 Journal of Pathology Informatics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Jain, Manu Robinson, Brian D. Salamoon, Bekheit Thouvenin, Olivier Boccara, Claude Mukherjee, Sushmita Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title | Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title_full | Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title_fullStr | Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title_full_unstemmed | Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title_short | Rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
title_sort | rapid evaluation of fresh ex vivo kidney tissue with full-field optical coherence tomography |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629311/ https://www.ncbi.nlm.nih.gov/pubmed/26605118 http://dx.doi.org/10.4103/2153-3539.166014 |
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