Type 2 segmental glomangioma - Case report
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700097 |
Resumo: | Abstract Glomus tumors originate from modified perivascular muscle cells. The most common form is the solitary one. The multiple form may be associated with dominant genetic inheritance. We report a case of a patient with hemangiomatous lesions on the calcaneus and wrist since birth. In 6 years, there was progression of lesions throughout the body. Multiple glomangiomas are asymptomatic and more common in childhood. They can be confused with other vascular malformations. Histopathological diagnosis is essential. The case shows a type 2 segmental manifestation that can be explained by genetic mutation leading to the loss of heterozygosity. As the child grows, the lesions may disseminate due to mutation in distant parts of the skin. Literature shows few reports. The treatment is conservative. |
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Anais brasileiros de dermatologia (Online) |
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Type 2 segmental glomangioma - Case reportClassificationCongenital abnormalitiesGlomus tumorInternational classification of diseasesVascular malformationsAbstract Glomus tumors originate from modified perivascular muscle cells. The most common form is the solitary one. The multiple form may be associated with dominant genetic inheritance. We report a case of a patient with hemangiomatous lesions on the calcaneus and wrist since birth. In 6 years, there was progression of lesions throughout the body. Multiple glomangiomas are asymptomatic and more common in childhood. They can be confused with other vascular malformations. Histopathological diagnosis is essential. The case shows a type 2 segmental manifestation that can be explained by genetic mutation leading to the loss of heterozygosity. As the child grows, the lesions may disseminate due to mutation in distant parts of the skin. Literature shows few reports. The treatment is conservative.Sociedade Brasileira de Dermatologia2015-06-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700097Anais Brasileiros de Dermatologia v.90 n.3 suppl.1 2015reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20152483info:eu-repo/semantics/openAccessCabral,Camila RaposoOliveira Filho,Jayme deMatsumoto,Julliene LikaCignachi,StelaTebet,Ana Carolina FrancoNasser,Kássila da Rosaeng2015-11-19T00:00:00Zoai:scielo:S0365-05962015000700097Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2015-11-19T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Type 2 segmental glomangioma - Case report |
title |
Type 2 segmental glomangioma - Case report |
spellingShingle |
Type 2 segmental glomangioma - Case report Cabral,Camila Raposo Classification Congenital abnormalities Glomus tumor International classification of diseases Vascular malformations |
title_short |
Type 2 segmental glomangioma - Case report |
title_full |
Type 2 segmental glomangioma - Case report |
title_fullStr |
Type 2 segmental glomangioma - Case report |
title_full_unstemmed |
Type 2 segmental glomangioma - Case report |
title_sort |
Type 2 segmental glomangioma - Case report |
author |
Cabral,Camila Raposo |
author_facet |
Cabral,Camila Raposo Oliveira Filho,Jayme de Matsumoto,Julliene Lika Cignachi,Stela Tebet,Ana Carolina Franco Nasser,Kássila da Rosa |
author_role |
author |
author2 |
Oliveira Filho,Jayme de Matsumoto,Julliene Lika Cignachi,Stela Tebet,Ana Carolina Franco Nasser,Kássila da Rosa |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Cabral,Camila Raposo Oliveira Filho,Jayme de Matsumoto,Julliene Lika Cignachi,Stela Tebet,Ana Carolina Franco Nasser,Kássila da Rosa |
dc.subject.por.fl_str_mv |
Classification Congenital abnormalities Glomus tumor International classification of diseases Vascular malformations |
topic |
Classification Congenital abnormalities Glomus tumor International classification of diseases Vascular malformations |
description |
Abstract Glomus tumors originate from modified perivascular muscle cells. The most common form is the solitary one. The multiple form may be associated with dominant genetic inheritance. We report a case of a patient with hemangiomatous lesions on the calcaneus and wrist since birth. In 6 years, there was progression of lesions throughout the body. Multiple glomangiomas are asymptomatic and more common in childhood. They can be confused with other vascular malformations. Histopathological diagnosis is essential. The case shows a type 2 segmental manifestation that can be explained by genetic mutation leading to the loss of heterozygosity. As the child grows, the lesions may disseminate due to mutation in distant parts of the skin. Literature shows few reports. The treatment is conservative. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/report |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
report |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700097 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700097 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20152483 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
dc.source.none.fl_str_mv |
Anais Brasileiros de Dermatologia v.90 n.3 suppl.1 2015 reponame:Anais brasileiros de dermatologia (Online) instname:Sociedade Brasileira de Dermatologia (SBD) instacron:SBD |
instname_str |
Sociedade Brasileira de Dermatologia (SBD) |
instacron_str |
SBD |
institution |
SBD |
reponame_str |
Anais brasileiros de dermatologia (Online) |
collection |
Anais brasileiros de dermatologia (Online) |
repository.name.fl_str_mv |
Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD) |
repository.mail.fl_str_mv |
abd@sbd.org.br||revista@sbd.org.br |
_version_ |
1752126420660781056 |