Case Report: Kaposiform Hemangioendothelioma in Multiple Spinal Levels Without Skin Changes
Identifieur interne : 000A10 ( Pmc/Curation ); précédent : 000A09; suivant : 000A11Case Report: Kaposiform Hemangioendothelioma in Multiple Spinal Levels Without Skin Changes
Auteurs : Jennifer W. Lisle [États-Unis] ; Heather A. Bradeen [États-Unis] ; Alexandra N. Kalof [États-Unis]Source :
- Clinical Orthopaedics and Related Research [ 0009-921X ] ; 2009.
Abstract
Kaposiform hemangioendothelioma is a rare vascular tumor of childhood that is locally aggressive but has little metastatic potential and by itself is not known to be lethal. It most commonly presents as a superficial or deep soft tissue mass with associated cutaneous lesions. Kasabach-Merritt phenomenon, a condition characterized by profound thrombocytopenia and life-threatening hemorrhage, often is associated with kaposiform hemangioendothelioma. Six cases of kaposiform hemangioendothelioma have been reported in bone, two of which were located in extracraniofacial bones. We report a diagnostically challenging case of a 6-year-old girl with kaposiform hemangioendothelioma of the thoracolumbar spine without Kasabach-Merritt phenomenon or cutaneous lesions.
Url:
DOI: 10.1007/s11999-009-0838-2
PubMed: 19381744
PubMed Central: 2866913
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Lisle</name><affiliation wicri:level="2"><nlm:aff id="Aff1">Department of Orthopedics and Rehabilitation, University of Vermont/Fletcher Allen Health Care, 426C Stafford Hall, 95 Carrigan Avenue, Burlington, VT 05405-0084 USA</nlm:aff><country xml:lang="fr">États-Unis</country><placeName><region type="state">Vermont</region></placeName><wicri:cityArea>Department of Orthopedics and Rehabilitation, University of Vermont/Fletcher Allen Health Care, 426C Stafford Hall, 95 Carrigan Avenue, Burlington</wicri:cityArea></affiliation></author><author><name sortKey="Bradeen, Heather A" sort="Bradeen, Heather A" uniqKey="Bradeen H" first="Heather A." last="Bradeen">Heather A. Bradeen</name><affiliation wicri:level="2"><nlm:aff id="Aff2">Department of Pediatrics, Hematology/Oncology, University of Vermont/Fletcher Allen Health Care, Burlington, VT USA</nlm:aff><country>États-Unis</country><placeName><region type="state">Vermont</region></placeName><wicri:cityArea>Department of Pediatrics, Hematology/Oncology, University of Vermont/Fletcher Allen Health Care, Burlington</wicri:cityArea></affiliation></author><author><name sortKey="Kalof, Alexandra N" sort="Kalof, Alexandra N" uniqKey="Kalof A" first="Alexandra N." last="Kalof">Alexandra N. Kalof</name><affiliation wicri:level="2"><nlm:aff id="Aff3">Department of Pathology, University of Vermont/Fletcher Allen Health Care, Burlington, VT USA</nlm:aff><country>États-Unis</country><placeName><region type="state">Vermont</region></placeName><wicri:cityArea>Department of Pathology, University of Vermont/Fletcher Allen Health Care, Burlington</wicri:cityArea></affiliation></author></analytic><series><title level="j">Clinical Orthopaedics and Related Research</title><idno type="ISSN">0009-921X</idno><idno type="eISSN">1528-1132</idno><imprint><date when="2009">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Kaposiform hemangioendothelioma is a rare vascular tumor of childhood that is locally aggressive but has little metastatic potential and by itself is not known to be lethal. It most commonly presents as a superficial or deep soft tissue mass with associated cutaneous lesions. Kasabach-Merritt phenomenon, a condition characterized by profound thrombocytopenia and life-threatening hemorrhage, often is associated with kaposiform hemangioendothelioma. Six cases of kaposiform hemangioendothelioma have been reported in bone, two of which were located in extracraniofacial bones. We report a diagnostically challenging case of a 6-year-old girl with kaposiform hemangioendothelioma of the thoracolumbar spine without Kasabach-Merritt phenomenon or cutaneous lesions.</p></div></front></TEI><pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Clin Orthop Relat Res</journal-id><journal-title-group><journal-title>Clinical Orthopaedics and Related Research</journal-title></journal-title-group><issn pub-type="ppub">0009-921X</issn><issn pub-type="epub">1528-1132</issn><publisher><publisher-name>Springer-Verlag</publisher-name><publisher-loc>New York</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">19381744</article-id><article-id pub-id-type="pmc">2866913</article-id><article-id pub-id-type="publisher-id">838</article-id><article-id pub-id-type="doi">10.1007/s11999-009-0838-2</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group></article-categories><title-group><article-title>Case Report: Kaposiform Hemangioendothelioma in Multiple Spinal Levels Without Skin Changes</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Lisle</surname><given-names>Jennifer W.</given-names></name><degrees>MD</degrees><address><email>jennifer.lisle@med.uvm.edu</email></address><xref ref-type="aff" rid="Aff1">1</xref></contrib><contrib contrib-type="author"><name><surname>Bradeen</surname><given-names>Heather A.</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Kalof</surname><given-names>Alexandra N.</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="Aff3">3</xref></contrib><aff id="Aff1"><label>1</label>Department of Orthopedics and Rehabilitation, University of Vermont/Fletcher Allen Health Care, 426C Stafford Hall, 95 Carrigan Avenue, Burlington, VT 05405-0084 USA</aff><aff id="Aff2"><label>2</label>Department of Pediatrics, Hematology/Oncology, University of Vermont/Fletcher Allen Health Care, Burlington, VT USA</aff><aff id="Aff3"><label>3</label>Department of Pathology, University of Vermont/Fletcher Allen Health Care, Burlington, VT USA</aff></contrib-group><pub-date pub-type="epub"><day>21</day><month>4</month><year>2009</year></pub-date><pub-date pub-type="ppub"><month>9</month><year>2009</year></pub-date><volume>467</volume><issue>9</issue><fpage>2464</fpage><lpage>2471</lpage><history><date date-type="received"><day>17</day><month>11</month><year>2008</year></date><date date-type="accepted"><day>1</day><month>4</month><year>2009</year></date></history><permissions><copyright-statement>© The Association of Bone and Joint Surgeons 2009</copyright-statement></permissions><abstract><p>Kaposiform hemangioendothelioma is a rare vascular tumor of childhood that is locally aggressive but has little metastatic potential and by itself is not known to be lethal. It most commonly presents as a superficial or deep soft tissue mass with associated cutaneous lesions. Kasabach-Merritt phenomenon, a condition characterized by profound thrombocytopenia and life-threatening hemorrhage, often is associated with kaposiform hemangioendothelioma. Six cases of kaposiform hemangioendothelioma have been reported in bone, two of which were located in extracraniofacial bones. We report a diagnostically challenging case of a 6-year-old girl with kaposiform hemangioendothelioma of the thoracolumbar spine without Kasabach-Merritt phenomenon or cutaneous lesions.</p></abstract><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© The Association of Bone and Joint Surgeons® 2009</meta-value></custom-meta></custom-meta-group></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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