Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.
Identifieur interne : 004E16 ( PubMed/Checkpoint ); précédent : 004E15; suivant : 004E17Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.
Auteurs : E. Calonje [Royaume-Uni] ; C D Fletcher ; E. Wilson-Jones ; J. RosaiSource :
- The American journal of surgical pathology [ 0147-5185 ] ; 1994.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Hémangioendothéliome, Hémangiosarcome, Tumeurs cutanées.
- Adolescent, Adulte, Adulte d'âge moyen, Diagnostic différentiel, Enfant, Femelle, Humains, Immunohistochimie, Mâle, Récidive.
English descriptors
- KwdEn :
- MESH :
Abstract
Fifteen cases of a distinctive type of low-grade angiosarcoma of the skin are described. Most tumors presented in the second to fourth decades of life, the youngest patient being 9 years old and the oldest 78 (mean age, 36 years). There was no sex predilection. Six tumors arose on the lower limb, four on the upper limb, three on the trunk, and one each on the penis and the scalp. One case arose in the setting of chronic lymphedema and another following radiotherapy for carcinoma of the uterine cervix. Distinctive morphologic features were the presence of long arborizing blood vessels arranged in a retiform pattern (reminiscent of normal rete testis) lined by monomorphic hobnail endothelial cells, a very prominent lymphocytic infiltrate in most cases, and the focal presence of papillae with hyaline collagenous cores, similar to those seen in malignant endovascular papillary angioendothelioma (Dabska's tumor). With a median follow-up of 7.25 years in 14 cases, retiform hemangioendothelioma has proved to be a low-grade neoplasm that recurs frequently but has a very low metastatic rate. The single regional lymph node metastasis in this series was from a case with a biphasic pattern in which only the spindle cell component was represented in the metastasis. There have been no tumor-related deaths, underlining the importance of accurate distinction from conventional angiosarcoma. This distinction is facilitated principally by the absence of dissection between individual collagen bundles and the absence of endothelial atypia or mitotic activity. The precise relationship between retiform hemangioendothelioma and Dabska's tumor is uncertain, possibly because cases of the latter may not be homogeneous.
PubMed: 8291650
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:8291650Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.</title><author><name sortKey="Calonje, E" sort="Calonje, E" uniqKey="Calonje E" first="E" last="Calonje">E. Calonje</name><affiliation wicri:level="2"><nlm:affiliation>Soft Tissue Tumour Unit, St. Thomas's Hospital, London, England.</nlm:affiliation><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>Soft Tissue Tumour Unit, St. Thomas's Hospital, London</wicri:cityArea></affiliation></author><author><name sortKey="Fletcher, C D" sort="Fletcher, C D" uniqKey="Fletcher C" first="C D" last="Fletcher">C D Fletcher</name></author><author><name sortKey="Wilson Jones, E" sort="Wilson Jones, E" uniqKey="Wilson Jones E" first="E" last="Wilson-Jones">E. Wilson-Jones</name></author><author><name sortKey="Rosai, J" sort="Rosai, J" uniqKey="Rosai J" first="J" last="Rosai">J. Rosai</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1994">1994</date><idno type="RBID">pubmed:8291650</idno><idno type="pmid">8291650</idno><idno type="wicri:Area/PubMed/Corpus">005592</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">005592</idno><idno type="wicri:Area/PubMed/Curation">005592</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">005592</idno><idno type="wicri:Area/PubMed/Checkpoint">005592</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">005592</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.</title><author><name sortKey="Calonje, E" sort="Calonje, E" uniqKey="Calonje E" first="E" last="Calonje">E. Calonje</name><affiliation wicri:level="2"><nlm:affiliation>Soft Tissue Tumour Unit, St. Thomas's Hospital, London, England.</nlm:affiliation><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>Soft Tissue Tumour Unit, St. Thomas's Hospital, London</wicri:cityArea></affiliation></author><author><name sortKey="Fletcher, C D" sort="Fletcher, C D" uniqKey="Fletcher C" first="C D" last="Fletcher">C D Fletcher</name></author><author><name sortKey="Wilson Jones, E" sort="Wilson Jones, E" uniqKey="Wilson Jones E" first="E" last="Wilson-Jones">E. Wilson-Jones</name></author><author><name sortKey="Rosai, J" sort="Rosai, J" uniqKey="Rosai J" first="J" last="Rosai">J. Rosai</name></author></analytic><series><title level="j">The American journal of surgical pathology</title><idno type="ISSN">0147-5185</idno><imprint><date when="1994" type="published">1994</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Child</term><term>Diagnosis, Differential</term><term>Female</term><term>Hemangioendothelioma (pathology)</term><term>Hemangiosarcoma (pathology)</term><term>Humans</term><term>Immunohistochemistry</term><term>Male</term><term>Middle Aged</term><term>Recurrence</term><term>Skin Neoplasms (pathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term><term>Adulte</term><term>Adulte d'âge moyen</term><term>Diagnostic différentiel</term><term>Enfant</term><term>Femelle</term><term>Humains</term><term>Hémangioendothéliome (anatomopathologie)</term><term>Hémangiosarcome (anatomopathologie)</term><term>Immunohistochimie</term><term>Mâle</term><term>Récidive</term><term>Tumeurs cutanées (anatomopathologie)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Hémangioendothéliome</term><term>Hémangiosarcome</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Hemangioendothelioma</term><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Child</term><term>Diagnosis, Differential</term><term>Female</term><term>Humans</term><term>Immunohistochemistry</term><term>Male</term><term>Middle Aged</term><term>Recurrence</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term><term>Adulte</term><term>Adulte d'âge moyen</term><term>Diagnostic différentiel</term><term>Enfant</term><term>Femelle</term><term>Humains</term><term>Immunohistochimie</term><term>Mâle</term><term>Récidive</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Fifteen cases of a distinctive type of low-grade angiosarcoma of the skin are described. Most tumors presented in the second to fourth decades of life, the youngest patient being 9 years old and the oldest 78 (mean age, 36 years). There was no sex predilection. Six tumors arose on the lower limb, four on the upper limb, three on the trunk, and one each on the penis and the scalp. One case arose in the setting of chronic lymphedema and another following radiotherapy for carcinoma of the uterine cervix. Distinctive morphologic features were the presence of long arborizing blood vessels arranged in a retiform pattern (reminiscent of normal rete testis) lined by monomorphic hobnail endothelial cells, a very prominent lymphocytic infiltrate in most cases, and the focal presence of papillae with hyaline collagenous cores, similar to those seen in malignant endovascular papillary angioendothelioma (Dabska's tumor). With a median follow-up of 7.25 years in 14 cases, retiform hemangioendothelioma has proved to be a low-grade neoplasm that recurs frequently but has a very low metastatic rate. The single regional lymph node metastasis in this series was from a case with a biphasic pattern in which only the spindle cell component was represented in the metastasis. There have been no tumor-related deaths, underlining the importance of accurate distinction from conventional angiosarcoma. This distinction is facilitated principally by the absence of dissection between individual collagen bundles and the absence of endothelial atypia or mitotic activity. The precise relationship between retiform hemangioendothelioma and Dabska's tumor is uncertain, possibly because cases of the latter may not be homogeneous.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8291650</PMID><DateCreated><Year>1994</Year><Month>02</Month><Day>24</Day></DateCreated><DateCompleted><Year>1994</Year><Month>02</Month><Day>24</Day></DateCompleted><DateRevised><Year>2004</Year><Month>11</Month><Day>17</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0147-5185</ISSN><JournalIssue CitedMedium="Print"><Volume>18</Volume><Issue>2</Issue><PubDate><Year>1994</Year><Month>Feb</Month></PubDate></JournalIssue><Title>The American journal of surgical pathology</Title><ISOAbbreviation>Am. J. Surg. Pathol.</ISOAbbreviation></Journal><ArticleTitle>Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.</ArticleTitle><Pagination><MedlinePgn>115-25</MedlinePgn></Pagination><Abstract><AbstractText>Fifteen cases of a distinctive type of low-grade angiosarcoma of the skin are described. Most tumors presented in the second to fourth decades of life, the youngest patient being 9 years old and the oldest 78 (mean age, 36 years). There was no sex predilection. Six tumors arose on the lower limb, four on the upper limb, three on the trunk, and one each on the penis and the scalp. One case arose in the setting of chronic lymphedema and another following radiotherapy for carcinoma of the uterine cervix. Distinctive morphologic features were the presence of long arborizing blood vessels arranged in a retiform pattern (reminiscent of normal rete testis) lined by monomorphic hobnail endothelial cells, a very prominent lymphocytic infiltrate in most cases, and the focal presence of papillae with hyaline collagenous cores, similar to those seen in malignant endovascular papillary angioendothelioma (Dabska's tumor). With a median follow-up of 7.25 years in 14 cases, retiform hemangioendothelioma has proved to be a low-grade neoplasm that recurs frequently but has a very low metastatic rate. The single regional lymph node metastasis in this series was from a case with a biphasic pattern in which only the spindle cell component was represented in the metastasis. There have been no tumor-related deaths, underlining the importance of accurate distinction from conventional angiosarcoma. This distinction is facilitated principally by the absence of dissection between individual collagen bundles and the absence of endothelial atypia or mitotic activity. The precise relationship between retiform hemangioendothelioma and Dabska's tumor is uncertain, possibly because cases of the latter may not be homogeneous.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Calonje</LastName><ForeName>E</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Soft Tissue Tumour Unit, St. Thomas's Hospital, London, England.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Fletcher</LastName><ForeName>C D</ForeName><Initials>CD</Initials></Author><Author ValidYN="Y"><LastName>Wilson-Jones</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Rosai</LastName><ForeName>J</ForeName><Initials>J</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Am J Surg Pathol</MedlineTA><NlmUniqueID>7707904</NlmUniqueID><ISSNLinking>0147-5185</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006390" MajorTopicYN="N">Hemangioendothelioma</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012008" MajorTopicYN="N">Recurrence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1994</Year><Month>2</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1994</Year><Month>2</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1994</Year><Month>2</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">8291650</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Royaume-Uni</li></country><region><li>Angleterre</li></region></list><tree><noCountry><name sortKey="Fletcher, C D" sort="Fletcher, C D" uniqKey="Fletcher C" first="C D" last="Fletcher">C D Fletcher</name><name sortKey="Rosai, J" sort="Rosai, J" uniqKey="Rosai J" first="J" last="Rosai">J. Rosai</name><name sortKey="Wilson Jones, E" sort="Wilson Jones, E" uniqKey="Wilson Jones E" first="E" last="Wilson-Jones">E. Wilson-Jones</name></noCountry><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Calonje, E" sort="Calonje, E" uniqKey="Calonje E" first="E" last="Calonje">E. Calonje</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004E16 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 004E16 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= PubMed
|étape= Checkpoint
|type= RBID
|clé= pubmed:8291650
|texte= Retiform hemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i -Sk "pubmed:8291650" \
| HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |