Angiosarcoma: clinical and imaging features from head to toe.
Identifieur interne : 000781 ( Main/Exploration ); précédent : 000780; suivant : 000782Angiosarcoma: clinical and imaging features from head to toe.
Auteurs : Ayman H. Gaballah [États-Unis] ; Corey T. Jensen [États-Unis] ; Sarah Palmquist [États-Unis] ; Perry J. Pickhardt [États-Unis] ; Alper Duran [États-Unis] ; Gregory Broering [États-Unis] ; Khaled M. Elsayes [États-Unis]Source :
- The British journal of radiology [ 1748-880X ] ; 2017.
Descripteurs français
- KwdFr :
- Diagnostic différentiel, Facteurs de risque, Humains, Hémangiosarcome (anatomopathologie), Hémangiosarcome (imagerie diagnostique), Hémangiosarcome (étiologie), Pronostic, Récidive tumorale locale (anatomopathologie), Récidive tumorale locale (imagerie diagnostique), Stade de la tumeur, Valeur prédictive des tests.
- MESH :
- anatomopathologie : Hémangiosarcome, Récidive tumorale locale.
- imagerie diagnostique : Hémangiosarcome, Récidive tumorale locale.
- étiologie : Hémangiosarcome.
- Diagnostic différentiel, Facteurs de risque, Humains, Pronostic, Stade de la tumeur, Valeur prédictive des tests.
English descriptors
- KwdEn :
- MESH :
- diagnostic imaging : Hemangiosarcoma, Neoplasm Recurrence, Local.
- etiology : Hemangiosarcoma.
- pathology : Hemangiosarcoma, Neoplasm Recurrence, Local.
- Diagnosis, Differential, Humans, Neoplasm Staging, Predictive Value of Tests, Prognosis, Risk Factors.
Abstract
Angiosarcoma is a rare, aggressive subtype of soft-tissue sarcoma with a propensity for local recurrence and metastasis associated with a generally poor prognosis, unless diagnosed early. Given the vascular endothelial cell origin of angiosarcoma, tumours may develop in essentially any organ; however, there is a predilection for the skin where half of all tumours arise, increasing in prevalence with age. The most common risk factors are chronic lymphoedema and history of radiation. We review the most important radiological findings along the spectrum of angiosarcoma from head to toe throughout the body, including uncommon and rare locations. Key imaging features of angiosarcoma across multiple organ systems will be described, as well as the impact on management and prognosis.
DOI: 10.1259/bjr.20170039
PubMed: 28471264
Affiliations:
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Le document en format XML
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Gaballah</name><affiliation wicri:level="2"><nlm:affiliation>1 Department of Diagnostic Radiology, University of Missouri-Columbia, Columbia, MO, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>1 Department of Diagnostic Radiology, University of Missouri-Columbia, Columbia, MO</wicri:regionArea><placeName><region type="state">Missouri (État)</region></placeName></affiliation></author><author><name sortKey="Jensen, Corey T" sort="Jensen, Corey T" uniqKey="Jensen C" first="Corey T" last="Jensen">Corey T. Jensen</name><affiliation wicri:level="2"><nlm:affiliation>2 Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>2 Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="Palmquist, Sarah" sort="Palmquist, Sarah" uniqKey="Palmquist S" first="Sarah" last="Palmquist">Sarah Palmquist</name><affiliation wicri:level="2"><nlm:affiliation>3 Department of Diagnostic Radiology, Baylor College of Medicine, Houston, TX, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>3 Department of Diagnostic Radiology, Baylor College of Medicine, Houston, TX</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="Pickhardt, Perry J" sort="Pickhardt, Perry J" uniqKey="Pickhardt P" first="Perry J" last="Pickhardt">Perry J. 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Elsayes</name><affiliation wicri:level="2"><nlm:affiliation>2 Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>2 Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author></analytic><series><title level="j">The British journal of radiology</title><idno type="eISSN">1748-880X</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term><term>Hemangiosarcoma (diagnostic imaging)</term><term>Hemangiosarcoma (etiology)</term><term>Hemangiosarcoma (pathology)</term><term>Humans</term><term>Neoplasm Recurrence, Local (diagnostic imaging)</term><term>Neoplasm Recurrence, Local (pathology)</term><term>Neoplasm Staging</term><term>Predictive Value of Tests</term><term>Prognosis</term><term>Risk Factors</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Diagnostic différentiel</term><term>Facteurs de risque</term><term>Humains</term><term>Hémangiosarcome (anatomopathologie)</term><term>Hémangiosarcome (imagerie diagnostique)</term><term>Hémangiosarcome (étiologie)</term><term>Pronostic</term><term>Récidive tumorale locale (anatomopathologie)</term><term>Récidive tumorale locale (imagerie diagnostique)</term><term>Stade de la tumeur</term><term>Valeur prédictive des tests</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangiosarcome</term><term>Récidive tumorale locale</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Hemangiosarcoma</term><term>Neoplasm Recurrence, Local</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Hemangiosarcoma</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Hémangiosarcome</term><term>Récidive tumorale locale</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hemangiosarcoma</term><term>Neoplasm Recurrence, Local</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Hémangiosarcome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term><term>Humans</term><term>Neoplasm Staging</term><term>Predictive Value of Tests</term><term>Prognosis</term><term>Risk Factors</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Diagnostic différentiel</term><term>Facteurs de risque</term><term>Humains</term><term>Pronostic</term><term>Stade de la tumeur</term><term>Valeur prédictive des tests</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Angiosarcoma is a rare, aggressive subtype of soft-tissue sarcoma with a propensity for local recurrence and metastasis associated with a generally poor prognosis, unless diagnosed early. Given the vascular endothelial cell origin of angiosarcoma, tumours may develop in essentially any organ; however, there is a predilection for the skin where half of all tumours arise, increasing in prevalence with age. The most common risk factors are chronic lymphoedema and history of radiation. We review the most important radiological findings along the spectrum of angiosarcoma from head to toe throughout the body, including uncommon and rare locations. Key imaging features of angiosarcoma across multiple organ systems will be described, as well as the impact on management and prognosis.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Missouri (État)</li><li>Texas</li><li>Wisconsin</li></region></list><tree><country name="États-Unis"><region name="Missouri (État)"><name sortKey="Gaballah, Ayman H" sort="Gaballah, Ayman H" uniqKey="Gaballah A" first="Ayman H" last="Gaballah">Ayman H. Gaballah</name></region><name sortKey="Broering, Gregory" sort="Broering, Gregory" uniqKey="Broering G" first="Gregory" last="Broering">Gregory Broering</name><name sortKey="Duran, Alper" sort="Duran, Alper" uniqKey="Duran A" first="Alper" last="Duran">Alper Duran</name><name sortKey="Elsayes, Khaled M" sort="Elsayes, Khaled M" uniqKey="Elsayes K" first="Khaled M" last="Elsayes">Khaled M. Elsayes</name><name sortKey="Jensen, Corey T" sort="Jensen, Corey T" uniqKey="Jensen C" first="Corey T" last="Jensen">Corey T. Jensen</name><name sortKey="Palmquist, Sarah" sort="Palmquist, Sarah" uniqKey="Palmquist S" first="Sarah" last="Palmquist">Sarah Palmquist</name><name sortKey="Pickhardt, Perry J" sort="Pickhardt, Perry J" uniqKey="Pickhardt P" first="Perry J" last="Pickhardt">Perry J. Pickhardt</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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