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Fully automated dual-color dual-hapten silver in situ hybridization staining for MYC amplification: a diagnostic tool for discriminating secondary angiosarcoma.

Identifieur interne : 001788 ( PubMed/Curation ); précédent : 001787; suivant : 001789

Fully automated dual-color dual-hapten silver in situ hybridization staining for MYC amplification: a diagnostic tool for discriminating secondary angiosarcoma.

Auteurs : Jennifer S. Ko [États-Unis] ; Steven D. Billings ; Christopher P. Lanigan ; Darya Buehler ; Anthony P. Fernandez ; Raymond R. Tubbs

Source :

RBID : pubmed:24329959

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Abstract

MYC amplification occurs in post-radiation and chronic lymphedema-associated secondary angiosarcoma and some primary angiosarcomas. In this study, we tested the ability of automated dual-color dual-hapten in situ hybridization (DISH) staining to discriminate secondary angiosarcoma from radiation-associated atypical vascular lesions (AVL), and to correlate with fluorescence in situ hybridization (FISH) for MYC amplification.

DOI: 10.1111/cup.12278
PubMed: 24329959

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pubmed:24329959

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<term>Hemangiosarcoma (metabolism)</term>
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<term>Adulte</term>
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<term>Hybridation in situ ()</term>
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<term>Hybridation in situ</term>
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<front>
<div type="abstract" xml:lang="en">MYC amplification occurs in post-radiation and chronic lymphedema-associated secondary angiosarcoma and some primary angiosarcomas. In this study, we tested the ability of automated dual-color dual-hapten in situ hybridization (DISH) staining to discriminate secondary angiosarcoma from radiation-associated atypical vascular lesions (AVL), and to correlate with fluorescence in situ hybridization (FISH) for MYC amplification.</div>
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<DateCreated>
<Year>2014</Year>
<Month>03</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted>
<Year>2014</Year>
<Month>10</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised>
<Year>2014</Year>
<Month>03</Month>
<Day>04</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1600-0560</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>41</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2014</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Journal of cutaneous pathology</Title>
<ISOAbbreviation>J. Cutan. Pathol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Fully automated dual-color dual-hapten silver in situ hybridization staining for MYC amplification: a diagnostic tool for discriminating secondary angiosarcoma.</ArticleTitle>
<Pagination>
<MedlinePgn>286-92</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1111/cup.12278</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">MYC amplification occurs in post-radiation and chronic lymphedema-associated secondary angiosarcoma and some primary angiosarcomas. In this study, we tested the ability of automated dual-color dual-hapten in situ hybridization (DISH) staining to discriminate secondary angiosarcoma from radiation-associated atypical vascular lesions (AVL), and to correlate with fluorescence in situ hybridization (FISH) for MYC amplification.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Cases of secondary angiosarcoma, including 11 biopsies and 3 excisions from 11 patients, and 5 AVL biopsies from 5 patients, were examined by FISH and DISH. DISH staining was performed using the Dual Color Open Probe software on a Ventana Benchmark XT automated slide stainer. Metallic black silver (MYC) and reference CHR8 red signals were qualitatively and semi-quantitatively enumerated for tumor nuclei. Small and large clusters of silver signals were recorded as 6 or 12 signals, respectively. MYC amplification was defined as MYC/CHR8 ratio >2.0.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Where tissue was available for both DISH and FISH, all secondary angiosarcoma cases showed MYC amplification (11/11 = 100%) by both DISH and FISH. All AVL were negative for MYC amplification by both techniques (0/5 = 0%).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">In the current cohort, use of DISH identified all MYC amplified cases, and distinguished secondary angiosarcoma from AVL. DISH staining may be useful in distinguishing secondary angiosarcoma from AVL in challenging cases.</AbstractText>
<CopyrightInformation>© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
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<LastName>Ko</LastName>
<ForeName>Jennifer S</ForeName>
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<Affiliation>Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.</Affiliation>
</AffiliationInfo>
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<ForeName>Christopher P</ForeName>
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<ForeName>Raymond R</ForeName>
<Initials>RR</Initials>
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<Language>eng</Language>
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<Year>2014</Year>
<Month>01</Month>
<Day>22</Day>
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<MedlineTA>J Cutan Pathol</MedlineTA>
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<ISSNLinking>0303-6987</ISSNLinking>
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<NameOfSubstance UI="C489427">MYC protein, human</NameOfSubstance>
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<DescriptorName UI="D005784" MajorTopicYN="Y">Gene Amplification</DescriptorName>
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<DescriptorName UI="D012878" MajorTopicYN="Y">Skin Neoplasms</DescriptorName>
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</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">MYC</Keyword>
<Keyword MajorTopicYN="N">atypical vascular lesions</Keyword>
<Keyword MajorTopicYN="N">in situ hybridization</Keyword>
<Keyword MajorTopicYN="N">secondary angiosarcoma</Keyword>
<Keyword MajorTopicYN="N">soft tissue tumors</Keyword>
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