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Phacomatosis pigmentovascularis type IIa--case report
Majoriê Mergen Segatto1, Eloísa Unfer Schmitt2, Laura Netto Hagemann2
1Federal University for Health Sciences, Porto AlegreRS, Brazil.
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.
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