Ki-1-positive large-cell cutaneous lymphoma mimicking a Stewart-Treves angiosarcoma.
Identifieur interne : 00B282 ( Ncbi/Merge ); précédent : 00B281; suivant : 00B283Ki-1-positive large-cell cutaneous lymphoma mimicking a Stewart-Treves angiosarcoma.
Auteurs : M. Beylot-Barry [France] ; B. Vergier ; C. Beylot ; A. Demascarel ; M S DoutreSource :
- Dermatology (Basel, Switzerland) [ 1018-8665 ] ; 1995.
Descripteurs français
- KwdFr :
- ADN tumoral (analyse), Diagnostic différentiel, Humains, Hémangiosarcome (anatomopathologie), Hémangiosarcome (diagnostic), Immunohistochimie, Immunophénotypage, Lymphome à grandes cellules anaplasiques (), Lymphome à grandes cellules anaplasiques (anatomopathologie), Lymphome à grandes cellules anaplasiques (diagnostic), Lymphome à grandes cellules anaplasiques (immunologie), Mâle, Poignet, Réarrangement des gènes de la chaine bêta du récepteur pour l'antigène des cellules T, Sujet âgé, Technique de Southern, Tumeurs cutanées (), Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (diagnostic), Tumeurs cutanées (immunologie).
- MESH :
- analyse : ADN tumoral.
- anatomopathologie : Hémangiosarcome, Lymphome à grandes cellules anaplasiques, Tumeurs cutanées.
- diagnostic : Hémangiosarcome, Lymphome à grandes cellules anaplasiques, Tumeurs cutanées.
- immunologie : Lymphome à grandes cellules anaplasiques, Tumeurs cutanées.
- Diagnostic différentiel, Humains, Immunohistochimie, Immunophénotypage, Lymphome à grandes cellules anaplasiques, Mâle, Poignet, Réarrangement des gènes de la chaine bêta du récepteur pour l'antigène des cellules T, Sujet âgé, Technique de Southern, Tumeurs cutanées.
English descriptors
- KwdEn :
- Aged, Blotting, Southern, DNA, Neoplasm (analysis), Diagnosis, Differential, Gene Rearrangement, beta-Chain T-Cell Antigen Receptor, Hemangiosarcoma (diagnosis), Hemangiosarcoma (pathology), Humans, Immunohistochemistry, Immunophenotyping, Lymphoma, Large-Cell, Anaplastic (diagnosis), Lymphoma, Large-Cell, Anaplastic (immunology), Lymphoma, Large-Cell, Anaplastic (pathology), Lymphoma, Large-Cell, Anaplastic (therapy), Male, Skin Neoplasms (diagnosis), Skin Neoplasms (immunology), Skin Neoplasms (pathology), Skin Neoplasms (therapy), Wrist.
- MESH :
- chemical , analysis : DNA, Neoplasm.
- diagnosis : Hemangiosarcoma, Lymphoma, Large-Cell, Anaplastic, Skin Neoplasms.
- immunology : Lymphoma, Large-Cell, Anaplastic, Skin Neoplasms.
- pathology : Hemangiosarcoma, Lymphoma, Large-Cell, Anaplastic, Skin Neoplasms.
- therapy : Lymphoma, Large-Cell, Anaplastic, Skin Neoplasms.
- Aged, Blotting, Southern, Diagnosis, Differential, Gene Rearrangement, beta-Chain T-Cell Antigen Receptor, Humans, Immunohistochemistry, Immunophenotyping, Male, Wrist.
Abstract
Anaplastic large-cell cutaneous lymphomas (ALCL) represent a heterogeneous group. Primitive cutaneous lymphomas are exceptional, sometimes with a deceptive clinical aspect, but must be considered as a distinct clinicopathologic entity. We report a case of a cutaneous ALCL, appearing 7 years after a homolateral Hodgkin ganglionic lymphoma and occurring on a chronic lymphoedema of the arm. A Stewart-Treves angiosarcoma was suggested owing to its location, vascular aspect and low histologic differentiation. Immunohistochemistry was helpful in making the diagnosis of ALCL. Southern blotting analysis revealed a rearrangement of the beta-chain of the T-receptor gene, thus suggesting the T-cell origin of this lymphoma.
PubMed: 7894104
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Primitive cutaneous lymphomas are exceptional, sometimes with a deceptive clinical aspect, but must be considered as a distinct clinicopathologic entity. We report a case of a cutaneous ALCL, appearing 7 years after a homolateral Hodgkin ganglionic lymphoma and occurring on a chronic lymphoedema of the arm. A Stewart-Treves angiosarcoma was suggested owing to its location, vascular aspect and low histologic differentiation. Immunohistochemistry was helpful in making the diagnosis of ALCL. Southern blotting analysis revealed a rearrangement of the beta-chain of the T-receptor gene, thus suggesting the T-cell origin of this lymphoma.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7894104</PMID><DateCreated><Year>1995</Year><Month>04</Month><Day>25</Day></DateCreated><DateCompleted><Year>1995</Year><Month>04</Month><Day>25</Day></DateCompleted><DateRevised><Year>2007</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">1018-8665</ISSN><JournalIssue CitedMedium="Print"><Volume>190</Volume><Issue>1</Issue><PubDate><Year>1995</Year></PubDate></JournalIssue><Title>Dermatology (Basel, Switzerland)</Title><ISOAbbreviation>Dermatology (Basel)</ISOAbbreviation></Journal><ArticleTitle>Ki-1-positive large-cell cutaneous lymphoma mimicking a Stewart-Treves angiosarcoma.</ArticleTitle><Pagination><MedlinePgn>77-82</MedlinePgn></Pagination><Abstract><AbstractText>Anaplastic large-cell cutaneous lymphomas (ALCL) represent a heterogeneous group. Primitive cutaneous lymphomas are exceptional, sometimes with a deceptive clinical aspect, but must be considered as a distinct clinicopathologic entity. We report a case of a cutaneous ALCL, appearing 7 years after a homolateral Hodgkin ganglionic lymphoma and occurring on a chronic lymphoedema of the arm. A Stewart-Treves angiosarcoma was suggested owing to its location, vascular aspect and low histologic differentiation. Immunohistochemistry was helpful in making the diagnosis of ALCL. Southern blotting analysis revealed a rearrangement of the beta-chain of the T-receptor gene, thus suggesting the T-cell origin of this lymphoma.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Beylot-Barry</LastName><ForeName>M</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Service de Dermatologie, Hôpital du Haut-Lévêque, CHU de Bordeaux, Pessac, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Vergier</LastName><ForeName>B</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Beylot</LastName><ForeName>C</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Demascarel</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Doutre</LastName><ForeName>M S</ForeName><Initials>MS</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Dermatology</MedlineTA><NlmUniqueID>9203244</NlmUniqueID><ISSNLinking>1018-8665</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004273">DNA, Neoplasm</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015139" MajorTopicYN="N">Blotting, Southern</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004273" MajorTopicYN="N">DNA, Neoplasm</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003937" MajorTopicYN="N">Diagnosis, Differential</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015333" MajorTopicYN="N">Gene Rearrangement, beta-Chain T-Cell Antigen Receptor</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><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="D016130" MajorTopicYN="N">Immunophenotyping</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017728" MajorTopicYN="N">Lymphoma, Large-Cell, Anaplastic</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014953" MajorTopicYN="N">Wrist</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1995</Year><Month>1</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1995</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1995</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">7894104</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>France</li></country></list><tree><noCountry><name sortKey="Beylot, C" sort="Beylot, C" uniqKey="Beylot C" first="C" last="Beylot">C. Beylot</name><name sortKey="Demascarel, A" sort="Demascarel, A" uniqKey="Demascarel A" first="A" last="Demascarel">A. Demascarel</name><name sortKey="Doutre, M S" sort="Doutre, M S" uniqKey="Doutre M" first="M S" last="Doutre">M S Doutre</name><name sortKey="Vergier, B" sort="Vergier, B" uniqKey="Vergier B" first="B" last="Vergier">B. Vergier</name></noCountry><country name="France"><noRegion><name sortKey="Beylot Barry, M" sort="Beylot Barry, M" uniqKey="Beylot Barry M" first="M" last="Beylot-Barry">M. Beylot-Barry</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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