A Novel Approach to Processing Descemet Stripping Automated Endothelial Keratoplasty Specimens for Histopathologic Analysis
PURPOSE:To describe a new technique for handling Descemet stripping automated endothelial keratoplasty (DSAEK) specimens intraoperatively and during processing. METHODS:The processing method begins by adding a drop of eosin to the specimen intraoperatively, followed by submersion in 10% formalin sol...
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Veröffentlicht in: | Cornea 2010-12, Vol.29 (12), p.1452-1454 |
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creator | Steven Houston, Samuel K Morgan, Olga Olsakovsky, Leslie A Phillips, Paul M Ghazi, Nicola G |
description | PURPOSE:To describe a new technique for handling Descemet stripping automated endothelial keratoplasty (DSAEK) specimens intraoperatively and during processing.
METHODS:The processing method begins by adding a drop of eosin to the specimen intraoperatively, followed by submersion in 10% formalin solution. The specimen appears reddish, allowing for easy identification and is floated onto an immersed slide to maintain an unfolded flattened specimen. After bisection, one half is stained with hematoxylin and eosin and covered with a cover slip, whereas the other half is transferred to filter paper and a cassette and is submitted for paraffin embedding on the cut edge.
RESULTS:The technique reduces the chances of a specimen not surviving processing. The new method also allows for 2 views of DSAEK specimens, both topographical and cross-sectional, thus permitting analysis of endothelial cell density, spatial distribution of cells and guttae, endothelial cell count, and thickness measurements.
CONCLUSIONS:A novel technique for handling DSAEK specimens to prevent loss and folding, while also allowing for cross-sectional and topographical viewing is reported. |
doi_str_mv | 10.1097/ICO.0b013e3181da57f3 |
format | Article |
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METHODS:The processing method begins by adding a drop of eosin to the specimen intraoperatively, followed by submersion in 10% formalin solution. The specimen appears reddish, allowing for easy identification and is floated onto an immersed slide to maintain an unfolded flattened specimen. After bisection, one half is stained with hematoxylin and eosin and covered with a cover slip, whereas the other half is transferred to filter paper and a cassette and is submitted for paraffin embedding on the cut edge.
RESULTS:The technique reduces the chances of a specimen not surviving processing. The new method also allows for 2 views of DSAEK specimens, both topographical and cross-sectional, thus permitting analysis of endothelial cell density, spatial distribution of cells and guttae, endothelial cell count, and thickness measurements.
CONCLUSIONS:A novel technique for handling DSAEK specimens to prevent loss and folding, while also allowing for cross-sectional and topographical viewing is reported.</description><identifier>ISSN: 0277-3740</identifier><identifier>EISSN: 1536-4798</identifier><identifier>DOI: 10.1097/ICO.0b013e3181da57f3</identifier><identifier>PMID: 20847670</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Cell Count ; Descemet Membrane - pathology ; Descemet Stripping Endothelial Keratoplasty - methods ; Endothelium, Corneal - pathology ; Histocytological Preparation Techniques - methods ; Humans ; Specimen Handling - methods</subject><ispartof>Cornea, 2010-12, Vol.29 (12), p.1452-1454</ispartof><rights>Copyright © 2010 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3553-48ceb408feb9c9882cb8da3582ad1a68c885e092b8cbd7bae5496bfc1b9670453</citedby><cites>FETCH-LOGICAL-c3553-48ceb408feb9c9882cb8da3582ad1a68c885e092b8cbd7bae5496bfc1b9670453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20847670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steven Houston, Samuel K</creatorcontrib><creatorcontrib>Morgan, Olga</creatorcontrib><creatorcontrib>Olsakovsky, Leslie A</creatorcontrib><creatorcontrib>Phillips, Paul M</creatorcontrib><creatorcontrib>Ghazi, Nicola G</creatorcontrib><title>A Novel Approach to Processing Descemet Stripping Automated Endothelial Keratoplasty Specimens for Histopathologic Analysis</title><title>Cornea</title><addtitle>Cornea</addtitle><description>PURPOSE:To describe a new technique for handling Descemet stripping automated endothelial keratoplasty (DSAEK) specimens intraoperatively and during processing.
METHODS:The processing method begins by adding a drop of eosin to the specimen intraoperatively, followed by submersion in 10% formalin solution. The specimen appears reddish, allowing for easy identification and is floated onto an immersed slide to maintain an unfolded flattened specimen. After bisection, one half is stained with hematoxylin and eosin and covered with a cover slip, whereas the other half is transferred to filter paper and a cassette and is submitted for paraffin embedding on the cut edge.
RESULTS:The technique reduces the chances of a specimen not surviving processing. The new method also allows for 2 views of DSAEK specimens, both topographical and cross-sectional, thus permitting analysis of endothelial cell density, spatial distribution of cells and guttae, endothelial cell count, and thickness measurements.
CONCLUSIONS:A novel technique for handling DSAEK specimens to prevent loss and folding, while also allowing for cross-sectional and topographical viewing is reported.</description><subject>Cell Count</subject><subject>Descemet Membrane - pathology</subject><subject>Descemet Stripping Endothelial Keratoplasty - methods</subject><subject>Endothelium, Corneal - pathology</subject><subject>Histocytological Preparation Techniques - methods</subject><subject>Humans</subject><subject>Specimen Handling - methods</subject><issn>0277-3740</issn><issn>1536-4798</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9L7TAQxYMoep_6DUSyc1Vf0rRNuizXvzxRQV2XJJ3aaNrUJFUufnkrV9_ChauBmXPOcH4IHVByTEnJ_14ub46JIpQBo4I2Muct20ALmrMiyXgpNtGCpJwnjGdkB_0J4YkQwnmRbqOdlIiMF5ws0HuFr90rWFyNo3dSdzg6fOudhhDM8IhPIGjoIeK76M04fq6qKbpeRmjw6dC42IE10uJ_4GV0o5UhrvDdCNr0MATcOo8vTJgvMnbOukejcTVIuwom7KGtVtoA-19zFz2cnd4vL5Krm_PLZXWVaJbnLMmEBpUR0YIqdSlEqpVoJMtFKhsqC6GFyIGUqRJaNVxJyLOyUK2mqpwrZjnbRUfr3LnhywQh1r2ZW1krB3BTqAVNKWOUkVmZrZXauxA8tPXoTS_9qqak_qRez9Trn9Rn2-HXg0n10Pw3fWOeBWIteHM2gg_PdnoDX3cgbex-z_4AN6eUGA</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Steven Houston, Samuel K</creator><creator>Morgan, Olga</creator><creator>Olsakovsky, Leslie A</creator><creator>Phillips, Paul M</creator><creator>Ghazi, Nicola G</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201012</creationdate><title>A Novel Approach to Processing Descemet Stripping Automated Endothelial Keratoplasty Specimens for Histopathologic Analysis</title><author>Steven Houston, Samuel K ; Morgan, Olga ; Olsakovsky, Leslie A ; Phillips, Paul M ; Ghazi, Nicola G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3553-48ceb408feb9c9882cb8da3582ad1a68c885e092b8cbd7bae5496bfc1b9670453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cell Count</topic><topic>Descemet Membrane - pathology</topic><topic>Descemet Stripping Endothelial Keratoplasty - methods</topic><topic>Endothelium, Corneal - pathology</topic><topic>Histocytological Preparation Techniques - methods</topic><topic>Humans</topic><topic>Specimen Handling - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steven Houston, Samuel K</creatorcontrib><creatorcontrib>Morgan, Olga</creatorcontrib><creatorcontrib>Olsakovsky, Leslie A</creatorcontrib><creatorcontrib>Phillips, Paul M</creatorcontrib><creatorcontrib>Ghazi, Nicola G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cornea</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steven Houston, Samuel K</au><au>Morgan, Olga</au><au>Olsakovsky, Leslie A</au><au>Phillips, Paul M</au><au>Ghazi, Nicola G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Novel Approach to Processing Descemet Stripping Automated Endothelial Keratoplasty Specimens for Histopathologic Analysis</atitle><jtitle>Cornea</jtitle><addtitle>Cornea</addtitle><date>2010-12</date><risdate>2010</risdate><volume>29</volume><issue>12</issue><spage>1452</spage><epage>1454</epage><pages>1452-1454</pages><issn>0277-3740</issn><eissn>1536-4798</eissn><abstract>PURPOSE:To describe a new technique for handling Descemet stripping automated endothelial keratoplasty (DSAEK) specimens intraoperatively and during processing.
METHODS:The processing method begins by adding a drop of eosin to the specimen intraoperatively, followed by submersion in 10% formalin solution. The specimen appears reddish, allowing for easy identification and is floated onto an immersed slide to maintain an unfolded flattened specimen. After bisection, one half is stained with hematoxylin and eosin and covered with a cover slip, whereas the other half is transferred to filter paper and a cassette and is submitted for paraffin embedding on the cut edge.
RESULTS:The technique reduces the chances of a specimen not surviving processing. The new method also allows for 2 views of DSAEK specimens, both topographical and cross-sectional, thus permitting analysis of endothelial cell density, spatial distribution of cells and guttae, endothelial cell count, and thickness measurements.
CONCLUSIONS:A novel technique for handling DSAEK specimens to prevent loss and folding, while also allowing for cross-sectional and topographical viewing is reported.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>20847670</pmid><doi>10.1097/ICO.0b013e3181da57f3</doi><tpages>3</tpages></addata></record> |
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subjects | Cell Count Descemet Membrane - pathology Descemet Stripping Endothelial Keratoplasty - methods Endothelium, Corneal - pathology Histocytological Preparation Techniques - methods Humans Specimen Handling - methods |
title | A Novel Approach to Processing Descemet Stripping Automated Endothelial Keratoplasty Specimens for Histopathologic Analysis |
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