A case of phakomatosis pigmentovascularis association with congenital temporal alopecia / 대한피부과학회지
Korean Journal of Dermatology
; : 252-255, 1991.
Article
de Ko
| WPRIM
| ID: wpr-110682
Bibliothèque responsable:
WPRO
ABSTRACT
Phakomatosis pigmentovascularis is characterized by the coexistence of pigmentary and vascular nevi, which are occasionally associated with systemic organ involvement. We report a 12-year-old male, who showed bilateral nevus of Ota on the forehead, periorbital area, sclera and soft palate, nevus of Ito on the scapular area, mongolian spot on the sacral area and widespread nevus flammeus. He was also associated with congenital temporal alopecia on the lower portion of left temporal region since birth.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Palais mou
/
Sclère
/
Naevus de Ota
/
Tache lie de vin
/
Syndromes neurocutanés
/
Parturition
/
Tache mongoloïde
/
Alopécie
/
Front
/
Naevus
Limites du sujet:
Child
/
Humans
/
Male
langue:
Ko
Texte intégral:
Korean Journal of Dermatology
Année:
1991
Type:
Article