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1.
An. bras. dermatol ; 91(5,supl.1): 54-56, Sept.-Oct. 2016. graf
Artigo em Inglês | LILACS | ID: biblio-837925

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.


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Neoplasias Cutâneas/patologia , Síndromes Neurocutâneas/patologia , Melanose/patologia , Nevo Pigmentado/patologia , Pele/patologia , Mancha Vinho do Porto/patologia , Doenças Raras/patologia
2.
An. bras. dermatol ; 90(3,supl.1): 10-12, May-June 2015. tab, ilus
Artigo em Inglês | LILACS | ID: lil-755755

RESUMO

Abstract

Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. We discuss an entirely unique case of Phacomatosis pigmentovascularis with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita, which may represent a heretofore undescribed variant of phacomatosis pigmentovascularis.

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Assuntos
Humanos , Masculino , Adulto Jovem , Mancha Mongólica/patologia , Síndromes Neurocutâneas/patologia , Nevo de Ota/patologia , Mancha Vinho do Porto/patologia , Dermatopatias Vasculares/patologia , Neoplasias Cutâneas/patologia , Telangiectasia/congênito , Síndromes Neurocutâneas/classificação , Telangiectasia/patologia
3.
An. bras. dermatol ; 89(4): 669-670, Jul-Aug/2014. graf
Artigo em Inglês | LILACS | ID: lil-715549

RESUMO

We present an interesting case report of two sarcoid-like lesions on a port-wine stain (PWS) birthmark in a Brazilian patient which on investigation proved to be cutaneous leishmaniasis.


Assuntos
Adulto , Feminino , Humanos , Leishmaniose Cutânea/patologia , Mancha Vinho do Porto/patologia , Biópsia , Imuno-Histoquímica , Pele/patologia
4.
Saudi Medical Journal. 2009; 30 (6): 844-846
em Inglês | IMEMR | ID: emr-92758

RESUMO

Pyogenic granuloma is a common benign vascular lesion of the skin and mucosa. There are a few reports on the rare association between it and port wine stain, but there is no clear description of an association with neurofibromatosis type 1 in the literature. This report presents a 29-year-old Saudi male with Von Recklinghausen's disease with recurrent pyogenic granuloma on the nevus flammeus over his neck. He was treated with shave excision and electrocautery with clearance and no recurrence of pyogenic granuloma for the last 5 years follow-up


Assuntos
Humanos , Masculino , Recidiva , Mancha Vinho do Porto/patologia , Neurofibromatose 1 , Pescoço , Eletrocoagulação , Seguimentos
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