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Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells

This video demonstrates Shidham's method for preparation of cell blocks from liquid based cervicovaginal cytology specimens containing individually scattered cells and small cell groups. This technique uses HistoGel (Thermo Scientific) with conventional laboratory equipment. The use of cell blo...

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Autores principales: Varsegi, George M., Shidham, Vinod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148935/
https://www.ncbi.nlm.nih.gov/pubmed/19623160
http://dx.doi.org/10.3791/1316
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author Varsegi, George M.
Shidham, Vinod
author_facet Varsegi, George M.
Shidham, Vinod
author_sort Varsegi, George M.
collection PubMed
description This video demonstrates Shidham's method for preparation of cell blocks from liquid based cervicovaginal cytology specimens containing individually scattered cells and small cell groups. This technique uses HistoGel (Thermo Scientific) with conventional laboratory equipment. The use of cell block sections is a valuable ancillary tool for evaluation of non-gynecologic cytology. They enable the cytopathologist to study additional morphologic specimen detail including the architecture of the lesion. Most importantly, they allow for the evaluation of ancillary studies such as immunocytochemistry, in-situ hybridization tests (FISH/CISH) and in-situ polymerase chain reaction (PCR). Traditional cell block preparation techniques have mostly been applied to non-gynecologic cytology specimens, typically for body fluid effusions and fine needle aspiration biopsies. Liquid based cervicovaginal specimens are relatively less cellular than their non-gynecologic counterparts with many individual scattered cells. Because of this, adequate cellularity within the cell block sections is difficult to achieve. In addition, the histotechnologist sectioning the block cannot visualize the level at which the cells are at the highest concentration. Therefore, it is difficult to monitor the appropriate level at which sections can be selected to be transferred to the glass slides for testing. As a result, the area of the cell block with the cells of interest may be missed, either by cutting past or not cutting deep enough. Current protocol for Shidham's method addresses these issues. Although this protocol is standardized and reported for gynecologic liquid based cytology specimens, it can also be applied to non-gynecologic specimens such as effusion fluids, FNA, brushings, cyst contents etc for improved quality of diagnostic material in cell block sections.
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spelling pubmed-31489352011-08-16 Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells Varsegi, George M. Shidham, Vinod J Vis Exp Cellular Biology This video demonstrates Shidham's method for preparation of cell blocks from liquid based cervicovaginal cytology specimens containing individually scattered cells and small cell groups. This technique uses HistoGel (Thermo Scientific) with conventional laboratory equipment. The use of cell block sections is a valuable ancillary tool for evaluation of non-gynecologic cytology. They enable the cytopathologist to study additional morphologic specimen detail including the architecture of the lesion. Most importantly, they allow for the evaluation of ancillary studies such as immunocytochemistry, in-situ hybridization tests (FISH/CISH) and in-situ polymerase chain reaction (PCR). Traditional cell block preparation techniques have mostly been applied to non-gynecologic cytology specimens, typically for body fluid effusions and fine needle aspiration biopsies. Liquid based cervicovaginal specimens are relatively less cellular than their non-gynecologic counterparts with many individual scattered cells. Because of this, adequate cellularity within the cell block sections is difficult to achieve. In addition, the histotechnologist sectioning the block cannot visualize the level at which the cells are at the highest concentration. Therefore, it is difficult to monitor the appropriate level at which sections can be selected to be transferred to the glass slides for testing. As a result, the area of the cell block with the cells of interest may be missed, either by cutting past or not cutting deep enough. Current protocol for Shidham's method addresses these issues. Although this protocol is standardized and reported for gynecologic liquid based cytology specimens, it can also be applied to non-gynecologic specimens such as effusion fluids, FNA, brushings, cyst contents etc for improved quality of diagnostic material in cell block sections. MyJove Corporation 2009-07-21 /pmc/articles/PMC3148935/ /pubmed/19623160 http://dx.doi.org/10.3791/1316 Text en Copyright © 2009, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Cellular Biology
Varsegi, George M.
Shidham, Vinod
Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title_full Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title_fullStr Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title_full_unstemmed Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title_short Cell Block Preparation from Cytology Specimen with Predominance of Individually Scattered Cells
title_sort cell block preparation from cytology specimen with predominance of individually scattered cells
topic Cellular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3148935/
https://www.ncbi.nlm.nih.gov/pubmed/19623160
http://dx.doi.org/10.3791/1316
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