Phacomatosis pigmentovascularis of cesioflammea type
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
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=S0365-05962016001100054 |
Resumo: | Abstract Phacomatosis pigmentovascularis is a rare syndrome, defined as the simultaneous presence of vascular nevus and melanocytic nevus in the same patient. We report the case of a 53-year-old woman presented with dermal melanosis and extensive vascular nevus, which match the typical manifestations of phakomatosis pigmetovascularis of cesioflammea type, according to Happle's classification. The rare occurrence of this genodermatosis and the clinical exuberance of the skin lesions motivated this case report. |
id |
SBD-1_1359975a7d99f15133601838d6ebb189 |
---|---|
oai_identifier_str |
oai:scielo:S0365-05962016001100054 |
network_acronym_str |
SBD-1 |
network_name_str |
Anais brasileiros de dermatologia (Online) |
repository_id_str |
|
spelling |
Phacomatosis pigmentovascularis of cesioflammea typeMelanocytesNevusNevus of OtaPort-wine stainSkin abnormalitiesSkin pigmentationAbstract Phacomatosis pigmentovascularis is a rare syndrome, defined as the simultaneous presence of vascular nevus and melanocytic nevus in the same patient. We report the case of a 53-year-old woman presented with dermal melanosis and extensive vascular nevus, which match the typical manifestations of phakomatosis pigmetovascularis of cesioflammea type, according to Happle's classification. The rare occurrence of this genodermatosis and the clinical exuberance of the skin lesions motivated this case report.Sociedade Brasileira de Dermatologia2016-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100054Anais Brasileiros de Dermatologia v.91 n.5 suppl.1 2016reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20164516info:eu-repo/semantics/openAccessVillarreal,Delky Johanna VillarrealLeal,Fabianoeng2017-03-03T00:00:00Zoai:scielo:S0365-05962016001100054Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2017-03-03T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Phacomatosis pigmentovascularis of cesioflammea type |
title |
Phacomatosis pigmentovascularis of cesioflammea type |
spellingShingle |
Phacomatosis pigmentovascularis of cesioflammea type Villarreal,Delky Johanna Villarreal Melanocytes Nevus Nevus of Ota Port-wine stain Skin abnormalities Skin pigmentation |
title_short |
Phacomatosis pigmentovascularis of cesioflammea type |
title_full |
Phacomatosis pigmentovascularis of cesioflammea type |
title_fullStr |
Phacomatosis pigmentovascularis of cesioflammea type |
title_full_unstemmed |
Phacomatosis pigmentovascularis of cesioflammea type |
title_sort |
Phacomatosis pigmentovascularis of cesioflammea type |
author |
Villarreal,Delky Johanna Villarreal |
author_facet |
Villarreal,Delky Johanna Villarreal Leal,Fabiano |
author_role |
author |
author2 |
Leal,Fabiano |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Villarreal,Delky Johanna Villarreal Leal,Fabiano |
dc.subject.por.fl_str_mv |
Melanocytes Nevus Nevus of Ota Port-wine stain Skin abnormalities Skin pigmentation |
topic |
Melanocytes Nevus Nevus of Ota Port-wine stain Skin abnormalities Skin pigmentation |
description |
Abstract Phacomatosis pigmentovascularis is a rare syndrome, defined as the simultaneous presence of vascular nevus and melanocytic nevus in the same patient. We report the case of a 53-year-old woman presented with dermal melanosis and extensive vascular nevus, which match the typical manifestations of phakomatosis pigmetovascularis of cesioflammea type, according to Happle's classification. The rare occurrence of this genodermatosis and the clinical exuberance of the skin lesions motivated this case report. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-10-01 |
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=S0365-05962016001100054 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100054 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20164516 |
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.91 n.5 suppl.1 2016 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_ |
1752126421463990272 |