Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol

Specimens of bone marrow trephine biopsy (BMT) are transported and fixed in acetic acid–zinc–formalin fixative, decalcified in 10% formic acid–5% formaldehyde and processed with other specimens to paraffin-wax embedding. Sections, 1-μm-thick, are cut by experienced histotechnologists and used for ha...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical pathology 2006-09, Vol.59 (9), p.903-911
Hauptverfasser: Naresh, K N, Lampert, I, Hasserjian, R, Lykidis, D, Elderfield, K, Horncastle, D, Smith, N, Murray-Brown, W, Stamp, G W
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 911
container_issue 9
container_start_page 903
container_title Journal of clinical pathology
container_volume 59
creator Naresh, K N
Lampert, I
Hasserjian, R
Lykidis, D
Elderfield, K
Horncastle, D
Smith, N
Murray-Brown, W
Stamp, G W
description Specimens of bone marrow trephine biopsy (BMT) are transported and fixed in acetic acid–zinc–formalin fixative, decalcified in 10% formic acid–5% formaldehyde and processed with other specimens to paraffin-wax embedding. Sections, 1-μm-thick, are cut by experienced histotechnologists and used for haematoxylin and eosin, Giemsa, reticulin silver and other histological stains. Further, all immunohistochemical procedures used in the laboratory, including double immunostaining, can be used on these sections with no or minimal modifications. About 10 000 BMT specimens have been analysed using this procedure since 1997 and diseases involving the bone marrow have been classified successfully. More recently, standardised polymerase chain reaction-based analysis and mRNA in situ hybridisation studies have been conducted. Excellent morphology with good antigen, DNA and RNA preservation is offered by the Hammersmith Protocol.
doi_str_mv 10.1136/jcp.2004.020610
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1860463</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4022526381</sourcerecordid><originalsourceid>FETCH-LOGICAL-b522t-d43df22d580b6253fc93b4bf360dbe7de729042d38abdf5ee3df71aada897d953</originalsourceid><addsrcrecordid>eNqFkc1v1DAQxS0EokvhzA1FQnBAytbfjntAQivoIioKKnC17NjpekniYHuB_vd4yaoFLpxGo_nNm3l6ADxGcIkQ4SfbdlpiCOkSYsgRvAMWiApcU0T5XbCAEKNaCsqPwIOUthAiIhC5D44Ql4RJLhfg3cWU_aD7aoqhdSn58aoKXWXC6KpBxxh-VDm6aeNLb3yY0vVplTeuWuthcDENPm-qDzHk0Ib-IbjX6T65R4d6DD6_ef1pta7PL87erl6d14ZhnGtLie0wtqyBhmNGulYSQ01HOLTGCesElpBiSxptbMecK7hAWlvdSGElI8fg5aw77czgbOvGHHWvpliMxGsVtFd_T0a_UVfhu0INh5STIvD8IBDDt51LWQ0-ta7v9ejCLineCNnA35ee_gNuwy6OxZxCokEQMylEoU5mqo0hpei6m1cQVPuYVIlJ7WNSc0xl48mfDm75Qy4FeHYAdGp130U9tj7dcg0UEjJauHrmfMru581cx6-KCyKYev9lpS7ZGblcf2Rqf_jFzJth-98vfwGvL7iS</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1781025977</pqid></control><display><type>article</type><title>Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol</title><source>MEDLINE</source><source>BMJ Journals - NESLi2</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Naresh, K N ; Lampert, I ; Hasserjian, R ; Lykidis, D ; Elderfield, K ; Horncastle, D ; Smith, N ; Murray-Brown, W ; Stamp, G W</creator><creatorcontrib>Naresh, K N ; Lampert, I ; Hasserjian, R ; Lykidis, D ; Elderfield, K ; Horncastle, D ; Smith, N ; Murray-Brown, W ; Stamp, G W</creatorcontrib><description>Specimens of bone marrow trephine biopsy (BMT) are transported and fixed in acetic acid–zinc–formalin fixative, decalcified in 10% formic acid–5% formaldehyde and processed with other specimens to paraffin-wax embedding. Sections, 1-μm-thick, are cut by experienced histotechnologists and used for haematoxylin and eosin, Giemsa, reticulin silver and other histological stains. Further, all immunohistochemical procedures used in the laboratory, including double immunostaining, can be used on these sections with no or minimal modifications. About 10 000 BMT specimens have been analysed using this procedure since 1997 and diseases involving the bone marrow have been classified successfully. More recently, standardised polymerase chain reaction-based analysis and mRNA in situ hybridisation studies have been conducted. Excellent morphology with good antigen, DNA and RNA preservation is offered by the Hammersmith Protocol.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.2004.020610</identifier><identifier>PMID: 16935969</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>acetic acid–zinc–formalin ; Acids ; Antigens ; Automation ; AZF ; Biological and medical sciences ; Biopsy ; Biopsy - methods ; BMT ; Bone marrow ; Bone Marrow - pathology ; bone marrow biopsy using trephine ; Bone Marrow Examination - methods ; Bone Marrow Examination - standards ; Clinical Protocols ; DNA, Neoplasm - analysis ; EBV ; EDTA ; Epstein–Barr virus ; ethylene diamine tetra acetate ; H&amp;E ; haematoxylin and eosin ; Hematology ; Histopathology ; Humans ; in situ hybridisation ; Investigative techniques, diagnostic techniques (general aspects) ; ISH ; Laboratories ; Medical sciences ; Methods ; Morphology ; My Approach ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Polymerase Chain Reaction - methods ; Protocol ; Staining and Labeling - methods ; Tissue Fixation - methods</subject><ispartof>Journal of clinical pathology, 2006-09, Vol.59 (9), p.903-911</ispartof><rights>Copyright 2006 Journal of Clinical Pathology</rights><rights>2006 INIST-CNRS</rights><rights>Copyright: 2006 Copyright 2006 Journal of Clinical Pathology</rights><rights>Copyright © 2006 The BMJ Publishing Group and the Association of Clinical Pathologists</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b522t-d43df22d580b6253fc93b4bf360dbe7de729042d38abdf5ee3df71aada897d953</citedby><cites>FETCH-LOGICAL-b522t-d43df22d580b6253fc93b4bf360dbe7de729042d38abdf5ee3df71aada897d953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jcp.bmj.com/content/59/9/903.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jcp.bmj.com/content/59/9/903.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,230,314,723,776,780,881,3183,23550,27901,27902,53766,53768,77343,77374</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18079054$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16935969$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Naresh, K N</creatorcontrib><creatorcontrib>Lampert, I</creatorcontrib><creatorcontrib>Hasserjian, R</creatorcontrib><creatorcontrib>Lykidis, D</creatorcontrib><creatorcontrib>Elderfield, K</creatorcontrib><creatorcontrib>Horncastle, D</creatorcontrib><creatorcontrib>Smith, N</creatorcontrib><creatorcontrib>Murray-Brown, W</creatorcontrib><creatorcontrib>Stamp, G W</creatorcontrib><title>Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Specimens of bone marrow trephine biopsy (BMT) are transported and fixed in acetic acid–zinc–formalin fixative, decalcified in 10% formic acid–5% formaldehyde and processed with other specimens to paraffin-wax embedding. Sections, 1-μm-thick, are cut by experienced histotechnologists and used for haematoxylin and eosin, Giemsa, reticulin silver and other histological stains. Further, all immunohistochemical procedures used in the laboratory, including double immunostaining, can be used on these sections with no or minimal modifications. About 10 000 BMT specimens have been analysed using this procedure since 1997 and diseases involving the bone marrow have been classified successfully. More recently, standardised polymerase chain reaction-based analysis and mRNA in situ hybridisation studies have been conducted. Excellent morphology with good antigen, DNA and RNA preservation is offered by the Hammersmith Protocol.</description><subject>acetic acid–zinc–formalin</subject><subject>Acids</subject><subject>Antigens</subject><subject>Automation</subject><subject>AZF</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Biopsy - methods</subject><subject>BMT</subject><subject>Bone marrow</subject><subject>Bone Marrow - pathology</subject><subject>bone marrow biopsy using trephine</subject><subject>Bone Marrow Examination - methods</subject><subject>Bone Marrow Examination - standards</subject><subject>Clinical Protocols</subject><subject>DNA, Neoplasm - analysis</subject><subject>EBV</subject><subject>EDTA</subject><subject>Epstein–Barr virus</subject><subject>ethylene diamine tetra acetate</subject><subject>H&amp;E</subject><subject>haematoxylin and eosin</subject><subject>Hematology</subject><subject>Histopathology</subject><subject>Humans</subject><subject>in situ hybridisation</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>ISH</subject><subject>Laboratories</subject><subject>Medical sciences</subject><subject>Methods</subject><subject>Morphology</subject><subject>My Approach</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Protocol</subject><subject>Staining and Labeling - methods</subject><subject>Tissue Fixation - methods</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkc1v1DAQxS0EokvhzA1FQnBAytbfjntAQivoIioKKnC17NjpekniYHuB_vd4yaoFLpxGo_nNm3l6ADxGcIkQ4SfbdlpiCOkSYsgRvAMWiApcU0T5XbCAEKNaCsqPwIOUthAiIhC5D44Ql4RJLhfg3cWU_aD7aoqhdSn58aoKXWXC6KpBxxh-VDm6aeNLb3yY0vVplTeuWuthcDENPm-qDzHk0Ib-IbjX6T65R4d6DD6_ef1pta7PL87erl6d14ZhnGtLie0wtqyBhmNGulYSQ01HOLTGCesElpBiSxptbMecK7hAWlvdSGElI8fg5aw77czgbOvGHHWvpliMxGsVtFd_T0a_UVfhu0INh5STIvD8IBDDt51LWQ0-ta7v9ejCLineCNnA35ee_gNuwy6OxZxCokEQMylEoU5mqo0hpei6m1cQVPuYVIlJ7WNSc0xl48mfDm75Qy4FeHYAdGp130U9tj7dcg0UEjJauHrmfMru581cx6-KCyKYev9lpS7ZGblcf2Rqf_jFzJth-98vfwGvL7iS</recordid><startdate>20060901</startdate><enddate>20060901</enddate><creator>Naresh, K N</creator><creator>Lampert, I</creator><creator>Hasserjian, R</creator><creator>Lykidis, D</creator><creator>Elderfield, K</creator><creator>Horncastle, D</creator><creator>Smith, N</creator><creator>Murray-Brown, W</creator><creator>Stamp, G W</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>IQODW</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20060901</creationdate><title>Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol</title><author>Naresh, K N ; Lampert, I ; Hasserjian, R ; Lykidis, D ; Elderfield, K ; Horncastle, D ; Smith, N ; Murray-Brown, W ; Stamp, G W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b522t-d43df22d580b6253fc93b4bf360dbe7de729042d38abdf5ee3df71aada897d953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>acetic acid–zinc–formalin</topic><topic>Acids</topic><topic>Antigens</topic><topic>Automation</topic><topic>AZF</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Biopsy - methods</topic><topic>BMT</topic><topic>Bone marrow</topic><topic>Bone Marrow - pathology</topic><topic>bone marrow biopsy using trephine</topic><topic>Bone Marrow Examination - methods</topic><topic>Bone Marrow Examination - standards</topic><topic>Clinical Protocols</topic><topic>DNA, Neoplasm - analysis</topic><topic>EBV</topic><topic>EDTA</topic><topic>Epstein–Barr virus</topic><topic>ethylene diamine tetra acetate</topic><topic>H&amp;E</topic><topic>haematoxylin and eosin</topic><topic>Hematology</topic><topic>Histopathology</topic><topic>Humans</topic><topic>in situ hybridisation</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>ISH</topic><topic>Laboratories</topic><topic>Medical sciences</topic><topic>Methods</topic><topic>Morphology</topic><topic>My Approach</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Protocol</topic><topic>Staining and Labeling - methods</topic><topic>Tissue Fixation - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naresh, K N</creatorcontrib><creatorcontrib>Lampert, I</creatorcontrib><creatorcontrib>Hasserjian, R</creatorcontrib><creatorcontrib>Lykidis, D</creatorcontrib><creatorcontrib>Elderfield, K</creatorcontrib><creatorcontrib>Horncastle, D</creatorcontrib><creatorcontrib>Smith, N</creatorcontrib><creatorcontrib>Murray-Brown, W</creatorcontrib><creatorcontrib>Stamp, G W</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naresh, K N</au><au>Lampert, I</au><au>Hasserjian, R</au><au>Lykidis, D</au><au>Elderfield, K</au><au>Horncastle, D</au><au>Smith, N</au><au>Murray-Brown, W</au><au>Stamp, G W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>2006-09-01</date><risdate>2006</risdate><volume>59</volume><issue>9</issue><spage>903</spage><epage>911</epage><pages>903-911</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Specimens of bone marrow trephine biopsy (BMT) are transported and fixed in acetic acid–zinc–formalin fixative, decalcified in 10% formic acid–5% formaldehyde and processed with other specimens to paraffin-wax embedding. Sections, 1-μm-thick, are cut by experienced histotechnologists and used for haematoxylin and eosin, Giemsa, reticulin silver and other histological stains. Further, all immunohistochemical procedures used in the laboratory, including double immunostaining, can be used on these sections with no or minimal modifications. About 10 000 BMT specimens have been analysed using this procedure since 1997 and diseases involving the bone marrow have been classified successfully. More recently, standardised polymerase chain reaction-based analysis and mRNA in situ hybridisation studies have been conducted. Excellent morphology with good antigen, DNA and RNA preservation is offered by the Hammersmith Protocol.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>16935969</pmid><doi>10.1136/jcp.2004.020610</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9746
ispartof Journal of clinical pathology, 2006-09, Vol.59 (9), p.903-911
issn 0021-9746
1472-4146
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1860463
source MEDLINE; BMJ Journals - NESLi2; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects acetic acid–zinc–formalin
Acids
Antigens
Automation
AZF
Biological and medical sciences
Biopsy
Biopsy - methods
BMT
Bone marrow
Bone Marrow - pathology
bone marrow biopsy using trephine
Bone Marrow Examination - methods
Bone Marrow Examination - standards
Clinical Protocols
DNA, Neoplasm - analysis
EBV
EDTA
Epstein–Barr virus
ethylene diamine tetra acetate
H&E
haematoxylin and eosin
Hematology
Histopathology
Humans
in situ hybridisation
Investigative techniques, diagnostic techniques (general aspects)
ISH
Laboratories
Medical sciences
Methods
Morphology
My Approach
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Polymerase Chain Reaction - methods
Protocol
Staining and Labeling - methods
Tissue Fixation - methods
title Optimal processing of bone marrow trephine biopsy: the Hammersmith Protocol
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T17%3A53%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Optimal%20processing%20of%20bone%20marrow%20trephine%20biopsy:%20the%20Hammersmith%20Protocol&rft.jtitle=Journal%20of%20clinical%20pathology&rft.au=Naresh,%20K%20N&rft.date=2006-09-01&rft.volume=59&rft.issue=9&rft.spage=903&rft.epage=911&rft.pages=903-911&rft.issn=0021-9746&rft.eissn=1472-4146&rft.coden=JCPAAK&rft_id=info:doi/10.1136/jcp.2004.020610&rft_dat=%3Cproquest_pubme%3E4022526381%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1781025977&rft_id=info:pmid/16935969&rfr_iscdi=true