Steatocystoma multiplex suppurativa: case report of a rare condition
Autor(a) principal: | |
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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=S0365-05962016001100051 |
Resumo: | Abstract Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. This is the first case of steatocystoma multiplex suppurativa reported in the Brazilian literature. Female patient, 23 years old, with papular and nodular cystic lesions that started in the armpits and groin, later spreading to the trunk, lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular lesions associated with disseminated hidradenitis-like lesions in flexural areas and the histopathological diagnosis of steatocystoma defined the diagnosis of steatocystoma multiplex suppurativa. |
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Anais brasileiros de dermatologia (Online) |
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Steatocystoma multiplex suppurativa: case report of a rare conditionSteatocystoma MultiplexHidradenitis SuppurativaSuppurationAbstract Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. This is the first case of steatocystoma multiplex suppurativa reported in the Brazilian literature. Female patient, 23 years old, with papular and nodular cystic lesions that started in the armpits and groin, later spreading to the trunk, lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular lesions associated with disseminated hidradenitis-like lesions in flexural areas and the histopathological diagnosis of steatocystoma defined the diagnosis of steatocystoma multiplex suppurativa.Sociedade Brasileira de Dermatologia2016-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100051Anais Brasileiros de Dermatologia v.91 n.5 suppl.1 2016reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20164539info:eu-repo/semantics/openAccessSantana,Cândida Naira Lima e LimaPereira,Daniele do NascimentoLisboa,Alice PaixãoLeal,Juliana MartinsObadia,Daniel LagoSilva,Roberto Souto daeng2017-03-03T00:00:00Zoai:scielo:S0365-05962016001100051Revistahttp://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 |
Steatocystoma multiplex suppurativa: case report of a rare condition |
title |
Steatocystoma multiplex suppurativa: case report of a rare condition |
spellingShingle |
Steatocystoma multiplex suppurativa: case report of a rare condition Santana,Cândida Naira Lima e Lima Steatocystoma Multiplex Hidradenitis Suppurativa Suppuration |
title_short |
Steatocystoma multiplex suppurativa: case report of a rare condition |
title_full |
Steatocystoma multiplex suppurativa: case report of a rare condition |
title_fullStr |
Steatocystoma multiplex suppurativa: case report of a rare condition |
title_full_unstemmed |
Steatocystoma multiplex suppurativa: case report of a rare condition |
title_sort |
Steatocystoma multiplex suppurativa: case report of a rare condition |
author |
Santana,Cândida Naira Lima e Lima |
author_facet |
Santana,Cândida Naira Lima e Lima Pereira,Daniele do Nascimento Lisboa,Alice Paixão Leal,Juliana Martins Obadia,Daniel Lago Silva,Roberto Souto da |
author_role |
author |
author2 |
Pereira,Daniele do Nascimento Lisboa,Alice Paixão Leal,Juliana Martins Obadia,Daniel Lago Silva,Roberto Souto da |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Santana,Cândida Naira Lima e Lima Pereira,Daniele do Nascimento Lisboa,Alice Paixão Leal,Juliana Martins Obadia,Daniel Lago Silva,Roberto Souto da |
dc.subject.por.fl_str_mv |
Steatocystoma Multiplex Hidradenitis Suppurativa Suppuration |
topic |
Steatocystoma Multiplex Hidradenitis Suppurativa Suppuration |
description |
Abstract Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. This is the first case of steatocystoma multiplex suppurativa reported in the Brazilian literature. Female patient, 23 years old, with papular and nodular cystic lesions that started in the armpits and groin, later spreading to the trunk, lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular lesions associated with disseminated hidradenitis-like lesions in flexural areas and the histopathological diagnosis of steatocystoma defined the diagnosis of steatocystoma multiplex suppurativa. |
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=S0365-05962016001100051 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100051 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20164539 |
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_ |
1752126421461893120 |