Phacomatosis pigmentovascularis of cesioflammea type

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 manifestation...

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Main Authors: Delky Johanna Villarreal Villarreal, Fabiano Leal
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2016-10-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100054&tlng=en
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author Delky Johanna Villarreal Villarreal
Fabiano Leal
author_facet Delky Johanna Villarreal Villarreal
Fabiano Leal
author_sort Delky Johanna Villarreal Villarreal
collection DOAJ
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.
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spelling doaj.art-59c6293c40bb4087b1b9aac61019d4db2022-12-22T04:13:33ZengSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia0365-05962016-10-01915 suppl 1545610.1590/abd1806-4841.20164516Phacomatosis pigmentovascularis of cesioflammea typeDelky Johanna Villarreal VillarrealFabiano LealAbstract 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100054&tlng=enMelanocytesNevusNevus of OtaPort-wine stainSkin abnormalitiesSkin pigmentation
spellingShingle Delky Johanna Villarreal Villarreal
Fabiano Leal
Phacomatosis pigmentovascularis of cesioflammea type
Anais Brasileiros de Dermatologia
Melanocytes
Nevus
Nevus of Ota
Port-wine stain
Skin abnormalities
Skin pigmentation
title 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_short Phacomatosis pigmentovascularis of cesioflammea type
title_sort phacomatosis pigmentovascularis of cesioflammea type
topic Melanocytes
Nevus
Nevus of Ota
Port-wine stain
Skin abnormalities
Skin pigmentation
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962016001100054&tlng=en
work_keys_str_mv AT delkyjohannavillarrealvillarreal phacomatosispigmentovascularisofcesioflammeatype
AT fabianoleal phacomatosispigmentovascularisofcesioflammeatype