Correlation between histologic assessment and fluorescence in situ hybridization using MelanoSITE in evaluation of histologically ambiguous melanocytic lesions
The 4-probe, multicolor, fluorescence in situ hybridization (FISH) panel targeting chromosomes 6 and 11 has shown promising sensitivity and specificity in distinguishing between benign nevi and malignant melanoma. Only a few studies have assessed the potential utility of FISH in classification of hi...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2012-12, Vol.136 (12), p.1571-1579 |
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description | The 4-probe, multicolor, fluorescence in situ hybridization (FISH) panel targeting chromosomes 6 and 11 has shown promising sensitivity and specificity in distinguishing between benign nevi and malignant melanoma. Only a few studies have assessed the potential utility of FISH in classification of histologically ambiguous melanocytic lesions. In the United States, this assay is exclusively licensed to NeoGenomics Laboratories (Irvine, California), which provides the technical component and has developed an innovative service (MelanoSITE) allowing pathologists to interpret FISH results using a dedicated Web portal. Thus far, use of MelanoSITE as a diagnostic adjunct in the diagnosis of melanocytic lesions has not, to our knowledge, been reported in the literature.
To analyze 1.5 years of experience with the MelanoSITE melanoma FISH assay in the evaluation of histologically ambiguous lesions in the context of second opinion and routine dermatopathology practice.
A prospective histologic/FISH correlation study of 140 cases.
Twenty-seven percent of abnormal FISH results were false-positive results because of tetraploidy. After correcting for known false-positive results, all lesions considered atypical nevi showed normal FISH signals. Abnormal FISH signals were reported in 30% of lesions considered histologically borderline and in 48% of lesions in which a diagnosis of melanoma was favored.
Four-probe, multicolor FISH results for melanoma correlate with the microscopic assessments of histologically ambiguous lesions. Pathologists using MelanoSITE must be aware of the high rate of false-positive results from tetraploidy. |
doi_str_mv | 10.5858/arpa.2011-0673-OA |
format | Article |
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To analyze 1.5 years of experience with the MelanoSITE melanoma FISH assay in the evaluation of histologically ambiguous lesions in the context of second opinion and routine dermatopathology practice.
A prospective histologic/FISH correlation study of 140 cases.
Twenty-seven percent of abnormal FISH results were false-positive results because of tetraploidy. After correcting for known false-positive results, all lesions considered atypical nevi showed normal FISH signals. Abnormal FISH signals were reported in 30% of lesions considered histologically borderline and in 48% of lesions in which a diagnosis of melanoma was favored.
Four-probe, multicolor FISH results for melanoma correlate with the microscopic assessments of histologically ambiguous lesions. Pathologists using MelanoSITE must be aware of the high rate of false-positive results from tetraploidy.</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/arpa.2011-0673-OA</identifier><identifier>PMID: 22480223</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>Adolescent ; Adult ; Child ; Child, Preschool ; Chromosomes ; Cohort Studies ; Diagnosis ; Diagnosis, Differential ; False Positive Reactions ; Female ; Fluorescence ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Materials Testing ; Melanocytes - metabolism ; Melanocytes - pathology ; Melanoma ; Melanoma - diagnosis ; Melanoma - genetics ; Melanoma - metabolism ; Melanoma - pathology ; Melanoma-Specific Antigens - metabolism ; Middle Aged ; Nevus - diagnosis ; Nevus - genetics ; Nevus - metabolism ; Nevus - pathology ; Prospective Studies ; Reagent Kits, Diagnostic ; Sensitivity and Specificity ; Skin diseases ; Skin Neoplasms - diagnosis ; Skin Neoplasms - genetics ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology ; Tetraploidy ; Web portals ; Young Adult</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2012-12, Vol.136 (12), p.1571-1579</ispartof><rights>COPYRIGHT 2012 College of American Pathologists</rights><rights>Copyright College of American Pathologists Dec 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-3b64fd3fc3f34c649293a57dbccd179b2fffc12c8ae8c3f22b40505a40b69e003</citedby><cites>FETCH-LOGICAL-c465t-3b64fd3fc3f34c649293a57dbccd179b2fffc12c8ae8c3f22b40505a40b69e003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22480223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zembowicz, Artur</creatorcontrib><creatorcontrib>Yang, Sung-Eun</creatorcontrib><creatorcontrib>Kafanas, Antonios</creatorcontrib><creatorcontrib>Lyle, Stephen R</creatorcontrib><title>Correlation between histologic assessment and fluorescence in situ hybridization using MelanoSITE in evaluation of histologically ambiguous melanocytic lesions</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>The 4-probe, multicolor, fluorescence in situ hybridization (FISH) panel targeting chromosomes 6 and 11 has shown promising sensitivity and specificity in distinguishing between benign nevi and malignant melanoma. Only a few studies have assessed the potential utility of FISH in classification of histologically ambiguous melanocytic lesions. In the United States, this assay is exclusively licensed to NeoGenomics Laboratories (Irvine, California), which provides the technical component and has developed an innovative service (MelanoSITE) allowing pathologists to interpret FISH results using a dedicated Web portal. Thus far, use of MelanoSITE as a diagnostic adjunct in the diagnosis of melanocytic lesions has not, to our knowledge, been reported in the literature.
To analyze 1.5 years of experience with the MelanoSITE melanoma FISH assay in the evaluation of histologically ambiguous lesions in the context of second opinion and routine dermatopathology practice.
A prospective histologic/FISH correlation study of 140 cases.
Twenty-seven percent of abnormal FISH results were false-positive results because of tetraploidy. After correcting for known false-positive results, all lesions considered atypical nevi showed normal FISH signals. Abnormal FISH signals were reported in 30% of lesions considered histologically borderline and in 48% of lesions in which a diagnosis of melanoma was favored.
Four-probe, multicolor FISH results for melanoma correlate with the microscopic assessments of histologically ambiguous lesions. Pathologists using MelanoSITE must be aware of the high rate of false-positive results from tetraploidy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosomes</subject><subject>Cohort Studies</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>False Positive Reactions</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Materials Testing</subject><subject>Melanocytes - metabolism</subject><subject>Melanocytes - pathology</subject><subject>Melanoma</subject><subject>Melanoma - diagnosis</subject><subject>Melanoma - genetics</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>Melanoma-Specific Antigens - metabolism</subject><subject>Middle Aged</subject><subject>Nevus - diagnosis</subject><subject>Nevus - genetics</subject><subject>Nevus - metabolism</subject><subject>Nevus - pathology</subject><subject>Prospective Studies</subject><subject>Reagent Kits, Diagnostic</subject><subject>Sensitivity and Specificity</subject><subject>Skin diseases</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><subject>Tetraploidy</subject><subject>Web portals</subject><subject>Young Adult</subject><issn>0003-9985</issn><issn>1543-2165</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptks1u1DAUhSMEokPhAdggS0iITQb_xJlkORq1UKloFpS15TjXGVeOPdgxaHiZvioOU6BFIy8s2985vr4-RfGa4CVvePNBhr1cUkxIiesVK7frJ8WC8IqVlNT8abHAGLOybRt-VryI8TYvW0rJ8-KM0qrBlLJFcbfxIYCVk_EOdTD9AHBoZ-LkrR-MQjJGiHEENyHpeqRt8gGiAqcAGYeimRLaHbpgevPzaJKicQP6nD2d_3J1czFj8F3adDz2-oG9tPaA5NiZIfkU0fhbpA5TvthCzHh8WTzT0kZ4dT-fF18vL242n8rr7cerzfq6VFXNp5J1daV7phXTrFJ11dKWSb7qO6V6smo7qrVWhKpGQpMZSrsKc8xlhbu6hdym8-L90Xcf_LcEcRKjyc-0uSDIpQlCV6wm2XeV0bf_obc-BZerE4TxuuJNTdk_apAWhHHaT0Gq2VSsGcMNZritM1WeoAZwEKT1DrTJ24_45Qk-jx5Go04K3j0Q7EDaaRe9TfNfxMcgOYIq-BgDaLEPZpThIAgWc9rEnDYxp03MaRPbdda8ue9E6kbo_yr-xIv9AlVP0uQ</recordid><startdate>201212</startdate><enddate>201212</enddate><creator>Zembowicz, Artur</creator><creator>Yang, Sung-Eun</creator><creator>Kafanas, Antonios</creator><creator>Lyle, Stephen R</creator><general>College of American Pathologists</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>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201212</creationdate><title>Correlation between histologic assessment and fluorescence in situ hybridization using MelanoSITE in evaluation of histologically ambiguous melanocytic lesions</title><author>Zembowicz, Artur ; Yang, Sung-Eun ; Kafanas, Antonios ; Lyle, Stephen R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-3b64fd3fc3f34c649293a57dbccd179b2fffc12c8ae8c3f22b40505a40b69e003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromosomes</topic><topic>Cohort Studies</topic><topic>Diagnosis</topic><topic>Diagnosis, Differential</topic><topic>False Positive Reactions</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Materials Testing</topic><topic>Melanocytes - metabolism</topic><topic>Melanocytes - pathology</topic><topic>Melanoma</topic><topic>Melanoma - diagnosis</topic><topic>Melanoma - genetics</topic><topic>Melanoma - metabolism</topic><topic>Melanoma - pathology</topic><topic>Melanoma-Specific Antigens - metabolism</topic><topic>Middle Aged</topic><topic>Nevus - diagnosis</topic><topic>Nevus - genetics</topic><topic>Nevus - metabolism</topic><topic>Nevus - pathology</topic><topic>Prospective Studies</topic><topic>Reagent Kits, Diagnostic</topic><topic>Sensitivity and Specificity</topic><topic>Skin diseases</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>Tetraploidy</topic><topic>Web portals</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zembowicz, Artur</creatorcontrib><creatorcontrib>Yang, Sung-Eun</creatorcontrib><creatorcontrib>Kafanas, Antonios</creatorcontrib><creatorcontrib>Lyle, Stephen R</creatorcontrib><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>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</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>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zembowicz, Artur</au><au>Yang, Sung-Eun</au><au>Kafanas, Antonios</au><au>Lyle, Stephen R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation between histologic assessment and fluorescence in situ hybridization using MelanoSITE in evaluation of histologically ambiguous melanocytic lesions</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2012-12</date><risdate>2012</risdate><volume>136</volume><issue>12</issue><spage>1571</spage><epage>1579</epage><pages>1571-1579</pages><issn>0003-9985</issn><issn>1543-2165</issn><eissn>1543-2165</eissn><coden>APLMAS</coden><abstract>The 4-probe, multicolor, fluorescence in situ hybridization (FISH) panel targeting chromosomes 6 and 11 has shown promising sensitivity and specificity in distinguishing between benign nevi and malignant melanoma. Only a few studies have assessed the potential utility of FISH in classification of histologically ambiguous melanocytic lesions. In the United States, this assay is exclusively licensed to NeoGenomics Laboratories (Irvine, California), which provides the technical component and has developed an innovative service (MelanoSITE) allowing pathologists to interpret FISH results using a dedicated Web portal. Thus far, use of MelanoSITE as a diagnostic adjunct in the diagnosis of melanocytic lesions has not, to our knowledge, been reported in the literature.
To analyze 1.5 years of experience with the MelanoSITE melanoma FISH assay in the evaluation of histologically ambiguous lesions in the context of second opinion and routine dermatopathology practice.
A prospective histologic/FISH correlation study of 140 cases.
Twenty-seven percent of abnormal FISH results were false-positive results because of tetraploidy. After correcting for known false-positive results, all lesions considered atypical nevi showed normal FISH signals. Abnormal FISH signals were reported in 30% of lesions considered histologically borderline and in 48% of lesions in which a diagnosis of melanoma was favored.
Four-probe, multicolor FISH results for melanoma correlate with the microscopic assessments of histologically ambiguous lesions. Pathologists using MelanoSITE must be aware of the high rate of false-positive results from tetraploidy.</abstract><cop>United States</cop><pub>College of American Pathologists</pub><pmid>22480223</pmid><doi>10.5858/arpa.2011-0673-OA</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Child Child, Preschool Chromosomes Cohort Studies Diagnosis Diagnosis, Differential False Positive Reactions Female Fluorescence Humans In Situ Hybridization, Fluorescence Male Materials Testing Melanocytes - metabolism Melanocytes - pathology Melanoma Melanoma - diagnosis Melanoma - genetics Melanoma - metabolism Melanoma - pathology Melanoma-Specific Antigens - metabolism Middle Aged Nevus - diagnosis Nevus - genetics Nevus - metabolism Nevus - pathology Prospective Studies Reagent Kits, Diagnostic Sensitivity and Specificity Skin diseases Skin Neoplasms - diagnosis Skin Neoplasms - genetics Skin Neoplasms - metabolism Skin Neoplasms - pathology Tetraploidy Web portals Young Adult |
title | Correlation between histologic assessment and fluorescence in situ hybridization using MelanoSITE in evaluation of histologically ambiguous melanocytic lesions |
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