Intracapsular melanoma: a new pitfall for sentinel lymph node biopsy
Sentinel lymph node biopsy (SLNB) has become an established technique for the staging and treatment of cutaneous melanoma. 1, 2 SLNB is very accurate in predicting tumour burden in the remaining regional lymph node basin and is also the most important independent prognostic indicator for recurrence...
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Veröffentlicht in: | Journal of clinical pathology 2006-08, Vol.59 (8), p.891-892 |
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description | Sentinel lymph node biopsy (SLNB) has become an established technique for the staging and treatment of cutaneous melanoma. 1, 2 SLNB is very accurate in predicting tumour burden in the remaining regional lymph node basin and is also the most important independent prognostic indicator for recurrence and survival when compared with factors such as tumour thickness and ulceration. 1 Large retrospective studies have shown that positive sentinel lymph nodes (SLNs) contain metastatic foci of melanoma cells in the subcapsular, sinusoidal or parenchymal regions. The subcapsular region is most commonly associated and up to 86% of metastatic foci become seeded in this area. 3 An important caveat of SLNB, however, is the false positives which result from benign naevic cells present in the capsule (intracapsular) or trabeculae of SLNs. 4 It is the intracapsular location of these cells, as well as differences in immunostaining and atypia, that aids the pathologist in distinguishing benign naevic cells from metastatic foci. 3- 5 Indeed, false-positives resulting from benign naevic cells are a cause for concern and require further investigation. |
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The subcapsular region is most commonly associated and up to 86% of metastatic foci become seeded in this area. 3 An important caveat of SLNB, however, is the false positives which result from benign naevic cells present in the capsule (intracapsular) or trabeculae of SLNs. 4 It is the intracapsular location of these cells, as well as differences in immunostaining and atypia, that aids the pathologist in distinguishing benign naevic cells from metastatic foci. 3- 5 Indeed, false-positives resulting from benign naevic cells are a cause for concern and require further investigation.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>PMID: 16873576</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Biopsy ; Histology ; Humans ; Letter to the Editor ; Lymphatic Metastasis ; Lymphatic system ; Medical prognosis ; Melanoma ; Melanoma - secondary ; Metastasis ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - pathology</subject><ispartof>Journal of clinical pathology, 2006-08, Vol.59 (8), p.891-892</ispartof><rights>Copyright 2006 Journal of Clinical Pathology</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><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jcp.bmj.com/content/59/8/891.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jcp.bmj.com/content/59/8/891.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>115,230,314,723,776,780,881,23550,53766,53768,77343,77374</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16873576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Howell, B G</creatorcontrib><creatorcontrib>Lipa, J E</creatorcontrib><creatorcontrib>Ghazarian, D M</creatorcontrib><title>Intracapsular melanoma: a new pitfall for sentinel lymph node biopsy</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Sentinel lymph node biopsy (SLNB) has become an established technique for the staging and treatment of cutaneous melanoma. 1, 2 SLNB is very accurate in predicting tumour burden in the remaining regional lymph node basin and is also the most important independent prognostic indicator for recurrence and survival when compared with factors such as tumour thickness and ulceration. 1 Large retrospective studies have shown that positive sentinel lymph nodes (SLNs) contain metastatic foci of melanoma cells in the subcapsular, sinusoidal or parenchymal regions. The subcapsular region is most commonly associated and up to 86% of metastatic foci become seeded in this area. 3 An important caveat of SLNB, however, is the false positives which result from benign naevic cells present in the capsule (intracapsular) or trabeculae of SLNs. 4 It is the intracapsular location of these cells, as well as differences in immunostaining and atypia, that aids the pathologist in distinguishing benign naevic cells from metastatic foci. 3- 5 Indeed, false-positives resulting from benign naevic cells are a cause for concern and require further investigation.</description><subject>Biopsy</subject><subject>Histology</subject><subject>Humans</subject><subject>Letter to the Editor</subject><subject>Lymphatic Metastasis</subject><subject>Lymphatic system</subject><subject>Medical prognosis</subject><subject>Melanoma</subject><subject>Melanoma - secondary</subject><subject>Metastasis</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - pathology</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>eNpVkMtOwzAQRSMEoqXwC8gS60h2_EpZIEF5FVWwgW5HTuLQlMQOsQP073HVUmAxGmnu0Z07sxcNCZNJzAgT-9EQ44TEY8nEIDpybokxoZLQw2hARCopl2IYXU-N71SuWtfXqkONrpWxjTpHChn9idrKl6quUWk75LTxldE1qldNu0DGFhpllW3d6jg6CJTTJ9s-il5ub54n9_Hs6W46uZzFGeXMxyWXmHBNMOVKJQXhQhaKZVQwKoVQYUxyKZM0TciYiqJUlCaClZwVnONC53QUXWx82z5rdJHrdfYa2q5qVLcCqyr4r5hqAa_2A0gqMGMkGJxtDTr73mvnYWn7zoTMQGRKcFjHcKBO_67Z-f98LQDxBqic1187XXVvICSVHB7nE7h64Hw-owLS39xZs9zRC-9bB8u8hfU0t00o40Nw4GNIIR0TKPs6XFeU9BsnZY-7</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Howell, B G</creator><creator>Lipa, J E</creator><creator>Ghazarian, D M</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</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>5PM</scope></search><sort><creationdate>200608</creationdate><title>Intracapsular melanoma: a new pitfall for sentinel lymph node biopsy</title><author>Howell, B G ; Lipa, J E ; Ghazarian, D M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b354t-f57015e1035aa2d1567da4b3643766a0351c7728821936dfa33264f54d550dec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Biopsy</topic><topic>Histology</topic><topic>Humans</topic><topic>Letter to the Editor</topic><topic>Lymphatic Metastasis</topic><topic>Lymphatic system</topic><topic>Medical prognosis</topic><topic>Melanoma</topic><topic>Melanoma - secondary</topic><topic>Metastasis</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Skin Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Howell, B G</creatorcontrib><creatorcontrib>Lipa, J E</creatorcontrib><creatorcontrib>Ghazarian, D M</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</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 & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</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>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>Howell, B G</au><au>Lipa, J E</au><au>Ghazarian, D M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intracapsular melanoma: a new pitfall for sentinel lymph node biopsy</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>2006-08</date><risdate>2006</risdate><volume>59</volume><issue>8</issue><spage>891</spage><epage>892</epage><pages>891-892</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Sentinel lymph node biopsy (SLNB) has become an established technique for the staging and treatment of cutaneous melanoma. 1, 2 SLNB is very accurate in predicting tumour burden in the remaining regional lymph node basin and is also the most important independent prognostic indicator for recurrence and survival when compared with factors such as tumour thickness and ulceration. 1 Large retrospective studies have shown that positive sentinel lymph nodes (SLNs) contain metastatic foci of melanoma cells in the subcapsular, sinusoidal or parenchymal regions. 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subjects | Biopsy Histology Humans Letter to the Editor Lymphatic Metastasis Lymphatic system Medical prognosis Melanoma Melanoma - secondary Metastasis Sentinel Lymph Node Biopsy Skin Neoplasms - pathology |
title | Intracapsular melanoma: a new pitfall for sentinel lymph node biopsy |
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