Oculoectodermal syndrome: twentieth described case with new manifestations
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=S0365-05962016001100160 |
Resumo: | Abstract Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome: aplasia cutis congenita and epibulbar dermoids. Our case expands the clinical spectrum of the disease to include: diffuse hyperpigmentation (some following the Blaschko´s lines); hypopigmented skin areas on the trunk; arachnoid cyst on the right fronto-parietal border; rounded left side of the hippocampus; and dermoid cyst underlying the bulb-medullary transition. Our patient also reported infantile hemangioma on the right wrist and verrucous hemangioma on the left leg, the latter not previously described in the literature. |
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Anais brasileiros de dermatologia (Online) |
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Oculoectodermal syndrome: twentieth described case with new manifestationsAstigmatismDermoid CystEcchymosisHemangiomaHyperpigmentationHypopigmentationAbstract Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome: aplasia cutis congenita and epibulbar dermoids. Our case expands the clinical spectrum of the disease to include: diffuse hyperpigmentation (some following the Blaschko´s lines); hypopigmented skin areas on the trunk; arachnoid cyst on the right fronto-parietal border; rounded left side of the hippocampus; and dermoid cyst underlying the bulb-medullary transition. Our patient also reported infantile hemangioma on the right wrist and verrucous hemangioma on the left leg, the latter not previously described in the literature.Sociedade Brasileira de Dermatologia2016-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100160Anais Brasileiros de Dermatologia v.91 n.5 suppl.1 2016reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20164409info:eu-repo/semantics/openAccessFigueiras,Daniela de AlmeidaLeal,Deborah Maria de Castro BarbosaKozmhinsky,ValterQuerino,Marina Coutinho DominguesRegueira,Marina Genesia da SilvaStudart,Maria Gabriela de Moraiseng2017-03-03T00:00:00Zoai:scielo:S0365-05962016001100160Revistahttp://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 |
Oculoectodermal syndrome: twentieth described case with new manifestations |
title |
Oculoectodermal syndrome: twentieth described case with new manifestations |
spellingShingle |
Oculoectodermal syndrome: twentieth described case with new manifestations Figueiras,Daniela de Almeida Astigmatism Dermoid Cyst Ecchymosis Hemangioma Hyperpigmentation Hypopigmentation |
title_short |
Oculoectodermal syndrome: twentieth described case with new manifestations |
title_full |
Oculoectodermal syndrome: twentieth described case with new manifestations |
title_fullStr |
Oculoectodermal syndrome: twentieth described case with new manifestations |
title_full_unstemmed |
Oculoectodermal syndrome: twentieth described case with new manifestations |
title_sort |
Oculoectodermal syndrome: twentieth described case with new manifestations |
author |
Figueiras,Daniela de Almeida |
author_facet |
Figueiras,Daniela de Almeida Leal,Deborah Maria de Castro Barbosa Kozmhinsky,Valter Querino,Marina Coutinho Domingues Regueira,Marina Genesia da Silva Studart,Maria Gabriela de Morais |
author_role |
author |
author2 |
Leal,Deborah Maria de Castro Barbosa Kozmhinsky,Valter Querino,Marina Coutinho Domingues Regueira,Marina Genesia da Silva Studart,Maria Gabriela de Morais |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Figueiras,Daniela de Almeida Leal,Deborah Maria de Castro Barbosa Kozmhinsky,Valter Querino,Marina Coutinho Domingues Regueira,Marina Genesia da Silva Studart,Maria Gabriela de Morais |
dc.subject.por.fl_str_mv |
Astigmatism Dermoid Cyst Ecchymosis Hemangioma Hyperpigmentation Hypopigmentation |
topic |
Astigmatism Dermoid Cyst Ecchymosis Hemangioma Hyperpigmentation Hypopigmentation |
description |
Abstract Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the syndrome: aplasia cutis congenita and epibulbar dermoids. Our case expands the clinical spectrum of the disease to include: diffuse hyperpigmentation (some following the Blaschko´s lines); hypopigmented skin areas on the trunk; arachnoid cyst on the right fronto-parietal border; rounded left side of the hippocampus; and dermoid cyst underlying the bulb-medullary transition. Our patient also reported infantile hemangioma on the right wrist and verrucous hemangioma on the left leg, the latter not previously described in the literature. |
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=S0365-05962016001100160 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100160 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20164409 |
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_ |
1752126421749202944 |