Phacomatosis pigmentovascularis type IIa - case report / Facomatose pigmentovascular tipo IIa - relato de caso
An. bras. dermatol
;
88(6,supl.1): 85-88, Nov-Dec/2013. tab, graf
Article
in English
| LILACS
| ID: lil-696803
ABSTRACT
Phacomatosis Pigmentovascularis is a rare syndrome characterized by capillary malformation and pigmentary nevus. A case of a 2-year-old patient is reported, who presented extensive nevus flammeus and an aberrant Mongolian spot, without systemic disease, manifestations that allow us to classify this case as type IIa Phacomatosis Pigmentovascularis, according to Hasegawa's classification.
RESUMO
A Facomatose Pigmentovascular, síndrome rara, é caracterizada pela presença concomitante de malformação capilar e nevos pigmentares. Relata-se o caso de um paciente de dois anos de idade com malformação capilar extensa e mancha mongólica aberrante sem comprometimento sistêmico, manifestações que o incluem no tipo IIa na classificação da Facomatose Pigmentovascular, segundo Hasegawa.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Skin Neoplasms
/
Nevus of Ota
/
Neurocutaneous Syndromes
/
Mongolian Spot
Limits:
Child, preschool
/
Humans
/
Male
Language:
English
Journal:
An. bras. dermatol
Journal subject:
Dermatology
Year:
2013
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Federal University for Health Sciences/BR
Similar
MEDLINE
...
LILACS
LIS