Acquired vulvar lymphangioma: a case series with emphasis on expanding clinical contexts.
Identifieur interne : 006496 ( Ncbi/Merge ); précédent : 006495; suivant : 006497Acquired vulvar lymphangioma: a case series with emphasis on expanding clinical contexts.
Auteurs : Elba Carballo Nú Ez [Espagne] ; José Manuel Suárez Pe Aranda ; Mario San Martín Alonso ; José Antonio Ortiz-ReySource :
- International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists [ 1538-7151 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Lymphangiome, Tumeurs de la vulve.
- Adulte, Adulte d'âge moyen, Condylomes acuminés, Femelle, Humains, Maladie de Crohn, Récidive tumorale locale, Sujet âgé, Études de suivi.
English descriptors
- KwdEn :
- MESH :
- complications : Condylomata Acuminata, Crohn Disease.
- pathology : Lymphangioma, Vulvar Neoplasms.
- Adult, Aged, Female, Follow-Up Studies, Humans, Middle Aged, Neoplasm Recurrence, Local.
Abstract
Vulvar lymphangioma circumscriptum (LC) is an unusual benign condition, congenital or acquired, related to interference in the lymph drainage. Acquired cases are usually related to oncological surgical procedures. We report 6 cases of vulvar LC: 3 have been caused by surgery and radiotherapy for gynecologic cancer, whereas the other 3 have originated under benign conditions--Crohn disease, recurring episodes of cellulits, and lower limb lymphedema. In 3 of them, the initial clinical diagnosis was genital wart. Surgical exeresis was performed as the treatment of choice in 5 patients and there were 3 cases of recurrences. Diagnosis of this unusual condition is not always easy even after histopathologic examination. The possibility of vulvar LC should be taken into account as a possible diagnosis in patients with previous oncological surgery or genital warts refractory to the conventional treatment. In these cases, a biopsy of not only the epidermis but also the superficial dermis is recommendable to rule out inflammatory or tumoral processes. Knowledge on the features of this lesion can avoid unnecessary clinical and therapeutic procedures.
DOI: 10.1097/PGP.0b013e31829655cb
PubMed: 24681732
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Pontevedra Department of Pathology (J.M.S.P), Clinical Hospital and School of Medicine, Santiago de Compostela Department of Pathology (M.S.M.A, J.A.O.-R.), Clinical and University Hospital of Vigo, Vigo, Galicia</wicri:regionArea><wicri:noRegion>Galicia</wicri:noRegion></affiliation></author><author><name sortKey="Pe Aranda, Jose Manuel Suarez" sort="Pe Aranda, Jose Manuel Suarez" uniqKey="Pe Aranda J" first="José Manuel Suárez" last="Pe Aranda">José Manuel Suárez Pe Aranda</name></author><author><name sortKey="Alonso, Mario San Martin" sort="Alonso, Mario San Martin" uniqKey="Alonso M" first="Mario San Martín" last="Alonso">Mario San Martín Alonso</name></author><author><name sortKey="Ortiz Rey, Jose Antonio" sort="Ortiz Rey, Jose Antonio" uniqKey="Ortiz Rey J" first="José Antonio" last="Ortiz-Rey">José Antonio Ortiz-Rey</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="RBID">pubmed:24681732</idno><idno type="pmid">24681732</idno><idno type="doi">10.1097/PGP.0b013e31829655cb</idno><idno type="wicri:Area/PubMed/Corpus">001588</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001588</idno><idno type="wicri:Area/PubMed/Curation">001588</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001588</idno><idno type="wicri:Area/PubMed/Checkpoint">001588</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">001588</idno><idno type="wicri:Area/Ncbi/Merge">006496</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Acquired vulvar lymphangioma: a case series with emphasis on expanding clinical contexts.</title><author><name sortKey="Nu Ez, Elba Carballo" sort="Nu Ez, Elba Carballo" uniqKey="Nu Ez E" first="Elba Carballo" last="Nú Ez">Elba Carballo Nú Ez</name><affiliation wicri:level="1"><nlm:affiliation>Department of Obstetrics and Gynecology (E.C.N), Clinical and University Hospital of Ourense, Alcalde Gregorio Espino, Vigo. Pontevedra Department of Pathology (J.M.S.P), Clinical Hospital and School of Medicine, Santiago de Compostela Department of Pathology (M.S.M.A, J.A.O.-R.), Clinical and University Hospital of Vigo, Vigo, Galicia, Spain.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Department of Obstetrics and Gynecology (E.C.N), Clinical and University Hospital of Ourense, Alcalde Gregorio Espino, Vigo. Pontevedra Department of Pathology (J.M.S.P), Clinical Hospital and School of Medicine, Santiago de Compostela Department of Pathology (M.S.M.A, J.A.O.-R.), Clinical and University Hospital of Vigo, Vigo, Galicia</wicri:regionArea><wicri:noRegion>Galicia</wicri:noRegion></affiliation></author><author><name sortKey="Pe Aranda, Jose Manuel Suarez" sort="Pe Aranda, Jose Manuel Suarez" uniqKey="Pe Aranda J" first="José Manuel Suárez" last="Pe Aranda">José Manuel Suárez Pe Aranda</name></author><author><name sortKey="Alonso, Mario San Martin" sort="Alonso, Mario San Martin" uniqKey="Alonso M" first="Mario San Martín" last="Alonso">Mario San Martín Alonso</name></author><author><name sortKey="Ortiz Rey, Jose Antonio" sort="Ortiz Rey, Jose Antonio" uniqKey="Ortiz Rey J" first="José Antonio" last="Ortiz-Rey">José Antonio Ortiz-Rey</name></author></analytic><series><title level="j">International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists</title><idno type="eISSN">1538-7151</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aged</term><term>Condylomata Acuminata (complications)</term><term>Crohn Disease (complications)</term><term>Female</term><term>Follow-Up Studies</term><term>Humans</term><term>Lymphangioma (pathology)</term><term>Middle Aged</term><term>Neoplasm Recurrence, Local</term><term>Vulvar Neoplasms (pathology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Condylomes acuminés ()</term><term>Femelle</term><term>Humains</term><term>Lymphangiome (anatomopathologie)</term><term>Maladie de Crohn ()</term><term>Récidive tumorale locale</term><term>Sujet âgé</term><term>Tumeurs de la vulve (anatomopathologie)</term><term>Études de suivi</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphangiome</term><term>Tumeurs de la vulve</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Condylomata Acuminata</term><term>Crohn Disease</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphangioma</term><term>Vulvar Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Female</term><term>Follow-Up Studies</term><term>Humans</term><term>Middle Aged</term><term>Neoplasm Recurrence, Local</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Condylomes acuminés</term><term>Femelle</term><term>Humains</term><term>Maladie de Crohn</term><term>Récidive tumorale locale</term><term>Sujet âgé</term><term>Études de suivi</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Vulvar lymphangioma circumscriptum (LC) is an unusual benign condition, congenital or acquired, related to interference in the lymph drainage. Acquired cases are usually related to oncological surgical procedures. We report 6 cases of vulvar LC: 3 have been caused by surgery and radiotherapy for gynecologic cancer, whereas the other 3 have originated under benign conditions--Crohn disease, recurring episodes of cellulits, and lower limb lymphedema. In 3 of them, the initial clinical diagnosis was genital wart. Surgical exeresis was performed as the treatment of choice in 5 patients and there were 3 cases of recurrences. Diagnosis of this unusual condition is not always easy even after histopathologic examination. The possibility of vulvar LC should be taken into account as a possible diagnosis in patients with previous oncological surgery or genital warts refractory to the conventional treatment. In these cases, a biopsy of not only the epidermis but also the superficial dermis is recommendable to rule out inflammatory or tumoral processes. Knowledge on the features of this lesion can avoid unnecessary clinical and therapeutic procedures.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24681732</PMID><DateCreated><Year>2014</Year><Month>04</Month><Day>09</Day></DateCreated><DateCompleted><Year>2015</Year><Month>04</Month><Day>17</Day></DateCompleted><DateRevised><Year>2014</Year><Month>04</Month><Day>09</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1538-7151</ISSN><JournalIssue CitedMedium="Internet"><Volume>33</Volume><Issue>3</Issue><PubDate><Year>2014</Year><Month>May</Month></PubDate></JournalIssue><Title>International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists</Title><ISOAbbreviation>Int. J. Gynecol. Pathol.</ISOAbbreviation></Journal><ArticleTitle>Acquired vulvar lymphangioma: a case series with emphasis on expanding clinical contexts.</ArticleTitle><Pagination><MedlinePgn>235-40</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1097/PGP.0b013e31829655cb</ELocationID><Abstract><AbstractText>Vulvar lymphangioma circumscriptum (LC) is an unusual benign condition, congenital or acquired, related to interference in the lymph drainage. Acquired cases are usually related to oncological surgical procedures. We report 6 cases of vulvar LC: 3 have been caused by surgery and radiotherapy for gynecologic cancer, whereas the other 3 have originated under benign conditions--Crohn disease, recurring episodes of cellulits, and lower limb lymphedema. In 3 of them, the initial clinical diagnosis was genital wart. Surgical exeresis was performed as the treatment of choice in 5 patients and there were 3 cases of recurrences. Diagnosis of this unusual condition is not always easy even after histopathologic examination. The possibility of vulvar LC should be taken into account as a possible diagnosis in patients with previous oncological surgery or genital warts refractory to the conventional treatment. In these cases, a biopsy of not only the epidermis but also the superficial dermis is recommendable to rule out inflammatory or tumoral processes. Knowledge on the features of this lesion can avoid unnecessary clinical and therapeutic procedures.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Núñez</LastName><ForeName>Elba Carballo</ForeName><Initials>EC</Initials><AffiliationInfo><Affiliation>Department of Obstetrics and Gynecology (E.C.N), Clinical and University Hospital of Ourense, Alcalde Gregorio Espino, Vigo. Pontevedra Department of Pathology (J.M.S.P), Clinical Hospital and School of Medicine, Santiago de Compostela Department of Pathology (M.S.M.A, J.A.O.-R.), Clinical and University Hospital of Vigo, Vigo, Galicia, Spain.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Peñaranda</LastName><ForeName>José Manuel Suárez</ForeName><Initials>JM</Initials></Author><Author ValidYN="Y"><LastName>Alonso</LastName><ForeName>Mario San Martín</ForeName><Initials>MS</Initials></Author><Author ValidYN="Y"><LastName>Ortiz-Rey</LastName><ForeName>José Antonio</ForeName><Initials>JA</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Int J Gynecol Pathol</MedlineTA><NlmUniqueID>8214845</NlmUniqueID><ISSNLinking>0277-1691</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003218" MajorTopicYN="N">Condylomata Acuminata</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003424" MajorTopicYN="N">Crohn Disease</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005500" MajorTopicYN="N">Follow-Up Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008202" MajorTopicYN="N">Lymphangioma</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009364" MajorTopicYN="N">Neoplasm Recurrence, Local</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014846" MajorTopicYN="N">Vulvar Neoplasms</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>4</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>4</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2015</Year><Month>4</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">24681732</ArticleId><ArticleId IdType="doi">10.1097/PGP.0b013e31829655cb</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Espagne</li></country></list><tree><noCountry><name sortKey="Alonso, Mario San Martin" sort="Alonso, Mario San Martin" uniqKey="Alonso M" first="Mario San Martín" last="Alonso">Mario San Martín Alonso</name><name sortKey="Ortiz Rey, Jose Antonio" sort="Ortiz Rey, Jose Antonio" uniqKey="Ortiz Rey J" first="José Antonio" last="Ortiz-Rey">José Antonio Ortiz-Rey</name><name sortKey="Pe Aranda, Jose Manuel Suarez" sort="Pe Aranda, Jose Manuel Suarez" uniqKey="Pe Aranda J" first="José Manuel Suárez" last="Pe Aranda">José Manuel Suárez Pe Aranda</name></noCountry><country name="Espagne"><noRegion><name sortKey="Nu Ez, Elba Carballo" sort="Nu Ez, Elba Carballo" uniqKey="Nu Ez E" first="Elba Carballo" last="Nú Ez">Elba Carballo Nú Ez</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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