MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity.
Identifieur interne : 008854 ( Ncbi/Merge ); précédent : 008853; suivant : 008855MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity.
Auteurs : David Harker [États-Unis] ; Michael Jennings [États-Unis] ; Patrick Mcdonough [États-Unis] ; Melissa Mauskar [États-Unis] ; Stephanie Savory [États-Unis] ; Gregory A. Hosler [États-Unis] ; Travis Vandergriff [États-Unis]Source :
- Journal of cutaneous pathology [ 1600-0560 ] ; 2017.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- Chronic Disease, Female, Gene Amplification, Hemangiosarcoma (complications), Hemangiosarcoma (genetics), Humans, In Situ Hybridization, Fluorescence, Lymphedema (etiology), Middle Aged, Obesity, Morbid (complications), Proto-Oncogene Proteins c-myc (genetics), Skin Neoplasms (complications), Skin Neoplasms (genetics).
- MESH :
- chemical , genetics : Proto-Oncogene Proteins c-myc.
- complications : Hemangiosarcoma, Obesity, Morbid, Skin Neoplasms.
- etiology : Lymphedema.
- genetics : Hemangiosarcoma, Skin Neoplasms.
- Chronic Disease, Female, Gene Amplification, Humans, In Situ Hybridization, Fluorescence, Middle Aged.
Abstract
Angiosarcoma is a malignancy of vascular endothelial cells which may arise secondarily as a complication of lymphedema, including chronic lymphedema of morbid obesity. Amplifications in MYC are frequently present in secondary angiosarcoma (arising in irradiated sites and chronic lymphedema) and less frequently in primary cutaneous angiosarcoma.
DOI: 10.1111/cup.12827
PubMed: 27686553
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000558
- to stream PubMed, to step Curation: 000558
- to stream PubMed, to step Checkpoint: 000558
Links to Exploration step
pubmed:27686553Le document en format XML
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<series><title level="j">Journal of cutaneous pathology</title>
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<term>Female</term>
<term>Gene Amplification</term>
<term>Hemangiosarcoma (complications)</term>
<term>Hemangiosarcoma (genetics)</term>
<term>Humans</term>
<term>In Situ Hybridization, Fluorescence</term>
<term>Lymphedema (etiology)</term>
<term>Middle Aged</term>
<term>Obesity, Morbid (complications)</term>
<term>Proto-Oncogene Proteins c-myc (genetics)</term>
<term>Skin Neoplasms (complications)</term>
<term>Skin Neoplasms (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Amplification de gène</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémangiosarcome ()</term>
<term>Hémangiosarcome (génétique)</term>
<term>Lymphoedème (étiologie)</term>
<term>Maladie chronique</term>
<term>Obésité morbide ()</term>
<term>Protéines proto-oncogènes c-myc (génétique)</term>
<term>Technique FISH</term>
<term>Tumeurs cutanées ()</term>
<term>Tumeurs cutanées (génétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Proto-Oncogene Proteins c-myc</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Obesity, Morbid</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hemangiosarcoma</term>
<term>Skin Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Hémangiosarcome</term>
<term>Protéines proto-oncogènes c-myc</term>
<term>Tumeurs cutanées</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chronic Disease</term>
<term>Female</term>
<term>Gene Amplification</term>
<term>Humans</term>
<term>In Situ Hybridization, Fluorescence</term>
<term>Middle Aged</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Amplification de gène</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémangiosarcome</term>
<term>Maladie chronique</term>
<term>Obésité morbide</term>
<term>Technique FISH</term>
<term>Tumeurs cutanées</term>
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<front><div type="abstract" xml:lang="en">Angiosarcoma is a malignancy of vascular endothelial cells which may arise secondarily as a complication of lymphedema, including chronic lymphedema of morbid obesity. Amplifications in MYC are frequently present in secondary angiosarcoma (arising in irradiated sites and chronic lymphedema) and less frequently in primary cutaneous angiosarcoma.</div>
</front>
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<DateCreated><Year>2016</Year>
<Month>09</Month>
<Day>30</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>08</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>08</Month>
<Day>17</Day>
</DateRevised>
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<JournalIssue CitedMedium="Internet"><Volume>44</Volume>
<Issue>1</Issue>
<PubDate><Year>2017</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Journal of cutaneous pathology</Title>
<ISOAbbreviation>J. Cutan. Pathol.</ISOAbbreviation>
</Journal>
<ArticleTitle>MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity.</ArticleTitle>
<Pagination><MedlinePgn>15-19</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/cup.12827</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Angiosarcoma is a malignancy of vascular endothelial cells which may arise secondarily as a complication of lymphedema, including chronic lymphedema of morbid obesity. Amplifications in MYC are frequently present in secondary angiosarcoma (arising in irradiated sites and chronic lymphedema) and less frequently in primary cutaneous angiosarcoma.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To describe the presence of MYC amplifications in two cases of cutaneous angiosarcoma secondary to chronic lymphedema of morbid obesity.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">This study is a case series of two patients with cutaneous angiosarcoma. Clinical data was retrieved from the medical records. Histopathological analysis of the biopsy specimens was performed, including immunohistochemistry, along with fluorescence in situ hybridization.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Angiosarcoma arose in the setting of massive chronic lymphedema complicating morbid obesity without other predisposing risk factors. Both cases exhibited epithelioid cell morphology and high-level MYC amplification.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">We report MYC amplification in two cases of angiosarcoma arising in massive chronic lymphedema of morbid obesity.</AbstractText>
<CopyrightInformation>© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Harker</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Jennings</LastName>
<ForeName>Michael</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Paul L. Foster School of Medicine, El Paso, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>McDonough</LastName>
<ForeName>Patrick</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Mauskar</LastName>
<ForeName>Melissa</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Savory</LastName>
<ForeName>Stephanie</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hosler</LastName>
<ForeName>Gregory A</ForeName>
<Initials>GA</Initials>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Vandergriff</LastName>
<ForeName>Travis</ForeName>
<Initials>T</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0001-6577-3838</Identifier>
<AffiliationInfo><Affiliation>Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
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<Month>10</Month>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C489427">MYC protein, human</NameOfSubstance>
</Chemical>
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<NameOfSubstance UI="D016271">Proto-Oncogene Proteins c-myc</NameOfSubstance>
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<MeshHeading><DescriptorName UI="D005784" MajorTopicYN="N">Gene Amplification</DescriptorName>
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<MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D017404" MajorTopicYN="N">In Situ Hybridization, Fluorescence</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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</MeshHeading>
<MeshHeading><DescriptorName UI="D016271" MajorTopicYN="N">Proto-Oncogene Proteins c-myc</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<name sortKey="Hosler, Gregory A" sort="Hosler, Gregory A" uniqKey="Hosler G" first="Gregory A" last="Hosler">Gregory A. Hosler</name>
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<name sortKey="Vandergriff, Travis" sort="Vandergriff, Travis" uniqKey="Vandergriff T" first="Travis" last="Vandergriff">Travis Vandergriff</name>
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