[Classification of vascular neoplasms].
Identifieur interne : 006601 ( PubMed/Checkpoint ); précédent : 006600; suivant : 006602[Classification of vascular neoplasms].
Auteurs : M. HundeikerSource :
- Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete [ 0017-8470 ] ; 1978.
Descripteurs français
- KwdFr :
- Complications postopératoires (diagnostic), Diagnostic différentiel, Humains, Hémangioendothéliome (diagnostic), Hémangiome (diagnostic), Hémangiome caverneux (diagnostic), Hémangiopéricytome (diagnostic), Lymphangiome (diagnostic), Lymphangiosarcome (diagnostic), Lymphoedème (diagnostic), Mastectomie, Naevus (diagnostic), Peau (), Sarcome de Kaposi (diagnostic), Syndrome, Tumeur glomique (diagnostic), Tumeurs cutanées (diagnostic), Tumeurs du tissu vasculaire ().
- MESH :
- diagnostic : Complications postopératoires, Hémangioendothéliome, Hémangiome, Hémangiome caverneux, Hémangiopéricytome, Lymphangiome, Lymphangiosarcome, Lymphoedème, Naevus, Sarcome de Kaposi, Tumeur glomique, Tumeurs cutanées.
- Diagnostic différentiel, Humains, Mastectomie, Peau, Syndrome, Tumeurs du tissu vasculaire.
English descriptors
- KwdEn :
- Diagnosis, Differential, Glomus Tumor (diagnosis), Hemangioendothelioma (diagnosis), Hemangioma (diagnosis), Hemangioma, Cavernous (diagnosis), Hemangiopericytoma (diagnosis), Humans, Lymphangioma (diagnosis), Lymphangiosarcoma (diagnosis), Lymphedema (diagnosis), Mastectomy, Neoplasms, Vascular Tissue (classification), Nevus (diagnosis), Postoperative Complications (diagnosis), Sarcoma, Kaposi (diagnosis), Skin (blood supply), Skin Neoplasms (diagnosis), Syndrome.
- MESH :
- blood supply : Skin.
- classification : Neoplasms, Vascular Tissue.
- diagnosis : Glomus Tumor, Hemangioendothelioma, Hemangioma, Hemangioma, Cavernous, Hemangiopericytoma, Lymphangioma, Lymphangiosarcoma, Lymphedema, Nevus, Postoperative Complications, Sarcoma, Kaposi, Skin Neoplasms.
- Diagnosis, Differential, Humans, Mastectomy, Syndrome.
Abstract
Neoplasms of blood and lymph vessels differ from angiectatic and angiokeratotic nevi by real proliferating growth. According to their features of growth and their wall structures, they are classified into three main groups: angiomas, glomangiomas and malignant vascular tumors. Within the angiomas on the one hand, capillary angiomas are classified into: planotuberous and tuberonodous angiomas of childhood and Kasabach-Merritt syndrome, multilocular hemangiomatosis, progressive multiple angiomas, tardive ("senile") angiomas, eruptive angiomas (granulomata pediculata), papular angioplasia, gemmangioma, and benign juvenile hemangioendothelioma. On the other hand, cavernous angiomas, i.e. arterial and venous cavernomas, as well as blue rubberbleb nevus, Mafucci's syndrome, angioleiomyoma, benign juvenile hemangiopericytoma and cavernous lymphangioma, form thick walled structures without involution. Glomangiomas occur as solitary, multiple systematized, and multiple disseminated and familiar forms. Within the group of malignant vascular tumors--Kaposi sarcoma, lymphangiosarcoma in lymphedema, hemangioendothelioma and angioplastic reticulosarcoma, hemangio- or lymphangiosarcoma, angioendotheliomastosis proliferans, rarity and increasing loss of characteristic differentiated structures give rise to difficulties in nosologic classification.
PubMed: 214413
Affiliations:
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Hundeiker</name></author></analytic><series><title level="j">Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete</title><idno type="ISSN">0017-8470</idno><imprint><date when="1978" type="published">1978</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term><term>Glomus Tumor (diagnosis)</term><term>Hemangioendothelioma (diagnosis)</term><term>Hemangioma (diagnosis)</term><term>Hemangioma, Cavernous (diagnosis)</term><term>Hemangiopericytoma (diagnosis)</term><term>Humans</term><term>Lymphangioma (diagnosis)</term><term>Lymphangiosarcoma (diagnosis)</term><term>Lymphedema (diagnosis)</term><term>Mastectomy</term><term>Neoplasms, Vascular Tissue (classification)</term><term>Nevus (diagnosis)</term><term>Postoperative Complications (diagnosis)</term><term>Sarcoma, Kaposi (diagnosis)</term><term>Skin (blood supply)</term><term>Skin Neoplasms (diagnosis)</term><term>Syndrome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Complications postopératoires (diagnostic)</term><term>Diagnostic différentiel</term><term>Humains</term><term>Hémangioendothéliome (diagnostic)</term><term>Hémangiome (diagnostic)</term><term>Hémangiome caverneux (diagnostic)</term><term>Hémangiopéricytome (diagnostic)</term><term>Lymphangiome (diagnostic)</term><term>Lymphangiosarcome (diagnostic)</term><term>Lymphoedème (diagnostic)</term><term>Mastectomie</term><term>Naevus (diagnostic)</term><term>Peau ()</term><term>Sarcome de Kaposi (diagnostic)</term><term>Syndrome</term><term>Tumeur glomique (diagnostic)</term><term>Tumeurs cutanées (diagnostic)</term><term>Tumeurs du tissu vasculaire ()</term></keywords><keywords scheme="MESH" qualifier="blood supply" xml:lang="en"><term>Skin</term></keywords><keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Neoplasms, Vascular Tissue</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Glomus Tumor</term><term>Hemangioendothelioma</term><term>Hemangioma</term><term>Hemangioma, Cavernous</term><term>Hemangiopericytoma</term><term>Lymphangioma</term><term>Lymphangiosarcoma</term><term>Lymphedema</term><term>Nevus</term><term>Postoperative Complications</term><term>Sarcoma, Kaposi</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Complications postopératoires</term><term>Hémangioendothéliome</term><term>Hémangiome</term><term>Hémangiome caverneux</term><term>Hémangiopéricytome</term><term>Lymphangiome</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Naevus</term><term>Sarcome de Kaposi</term><term>Tumeur glomique</term><term>Tumeurs cutanées</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term><term>Humans</term><term>Mastectomy</term><term>Syndrome</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Diagnostic différentiel</term><term>Humains</term><term>Mastectomie</term><term>Peau</term><term>Syndrome</term><term>Tumeurs du tissu vasculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Neoplasms of blood and lymph vessels differ from angiectatic and angiokeratotic nevi by real proliferating growth. According to their features of growth and their wall structures, they are classified into three main groups: angiomas, glomangiomas and malignant vascular tumors. Within the angiomas on the one hand, capillary angiomas are classified into: planotuberous and tuberonodous angiomas of childhood and Kasabach-Merritt syndrome, multilocular hemangiomatosis, progressive multiple angiomas, tardive ("senile") angiomas, eruptive angiomas (granulomata pediculata), papular angioplasia, gemmangioma, and benign juvenile hemangioendothelioma. On the other hand, cavernous angiomas, i.e. arterial and venous cavernomas, as well as blue rubberbleb nevus, Mafucci's syndrome, angioleiomyoma, benign juvenile hemangiopericytoma and cavernous lymphangioma, form thick walled structures without involution. Glomangiomas occur as solitary, multiple systematized, and multiple disseminated and familiar forms. Within the group of malignant vascular tumors--Kaposi sarcoma, lymphangiosarcoma in lymphedema, hemangioendothelioma and angioplastic reticulosarcoma, hemangio- or lymphangiosarcoma, angioendotheliomastosis proliferans, rarity and increasing loss of characteristic differentiated structures give rise to difficulties in nosologic classification.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">214413</PMID><DateCreated><Year>1979</Year><Month>02</Month><Day>21</Day></DateCreated><DateCompleted><Year>1979</Year><Month>02</Month><Day>21</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0017-8470</ISSN><JournalIssue CitedMedium="Print"><Volume>29</Volume><Issue>11</Issue><PubDate><Year>1978</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete</Title><ISOAbbreviation>Hautarzt</ISOAbbreviation></Journal><ArticleTitle>[Classification of vascular neoplasms].</ArticleTitle><Pagination><MedlinePgn>565-72</MedlinePgn></Pagination><Abstract><AbstractText>Neoplasms of blood and lymph vessels differ from angiectatic and angiokeratotic nevi by real proliferating growth. According to their features of growth and their wall structures, they are classified into three main groups: angiomas, glomangiomas and malignant vascular tumors. Within the angiomas on the one hand, capillary angiomas are classified into: planotuberous and tuberonodous angiomas of childhood and Kasabach-Merritt syndrome, multilocular hemangiomatosis, progressive multiple angiomas, tardive ("senile") angiomas, eruptive angiomas (granulomata pediculata), papular angioplasia, gemmangioma, and benign juvenile hemangioendothelioma. On the other hand, cavernous angiomas, i.e. arterial and venous cavernomas, as well as blue rubberbleb nevus, Mafucci's syndrome, angioleiomyoma, benign juvenile hemangiopericytoma and cavernous lymphangioma, form thick walled structures without involution. Glomangiomas occur as solitary, multiple systematized, and multiple disseminated and familiar forms. Within the group of malignant vascular tumors--Kaposi sarcoma, lymphangiosarcoma in lymphedema, hemangioendothelioma and angioplastic reticulosarcoma, hemangio- or lymphangiosarcoma, angioendotheliomastosis proliferans, rarity and increasing loss of characteristic differentiated structures give rise to difficulties in nosologic classification.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hundeiker</LastName><ForeName>M</ForeName><Initials>M</Initials></Author></AuthorList><Language>ger</Language><PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><VernacularTitle>Systematik der vaskulären Neubildungen.</VernacularTitle></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Hautarzt</MedlineTA><NlmUniqueID>0372755</NlmUniqueID><ISSNLinking>0017-8470</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005918" MajorTopicYN="N">Glomus Tumor</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006390" MajorTopicYN="N">Hemangioendothelioma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006391" MajorTopicYN="N">Hemangioma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006392" MajorTopicYN="N">Hemangioma, Cavernous</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006393" MajorTopicYN="N">Hemangiopericytoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008202" MajorTopicYN="N">Lymphangioma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008408" MajorTopicYN="N">Mastectomy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009383" MajorTopicYN="N">Neoplasms, Vascular Tissue</DescriptorName><QualifierName UI="Q000145" MajorTopicYN="Y">classification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009506" MajorTopicYN="N">Nevus</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011183" MajorTopicYN="N">Postoperative Complications</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012514" MajorTopicYN="N">Sarcoma, Kaposi</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012867" MajorTopicYN="N">Skin</DescriptorName><QualifierName UI="Q000098" MajorTopicYN="N">blood supply</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading></MeshHeadingList><NumberOfReferences>40</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1978</Year><Month>11</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1978</Year><Month>11</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1978</Year><Month>11</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">214413</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Hundeiker, M" sort="Hundeiker, M" uniqKey="Hundeiker M" first="M" last="Hundeiker">M. 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