Phakomatosis Pigmentovascularis Associated with Pyogenic Granuloma as well as Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome
Annals of Dermatology
;
: 158-160, 2002.
Artículo
en Inglés
| WPRIM
| ID: wpr-158657
ABSTRACT
A 21-year-old Korean male was referred to our department in June, 1999 for the evaluation of extensive reddish patches and gray-bluish pigmentation since birth. Physical examination revealed two kinds of patches over the various parts of the body. Reddish patches suggesting nevus flammeus were located on the left side of face, chest, and both upper and lower extremities. Gray-bluish pigmented patches suggesting nevus of Ota were found on both the periorbital areas. A 0.5×0.6 cm erythematous papule was found on the right anterior chest. The results of its histopathologic examination were compatible with pyogenic granuloma. We made the diagnosis of phakomatosis pigmentovascularis associated with pyogenic granuloma as well as Sturge-Weber syndrome and Klippel-Trenanunay syndrome.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Examen Físico
/
Tórax
/
Pigmentación
/
Síndrome de Sturge-Weber
/
Nevo de Ota
/
Granuloma Piogénico
/
Síndrome de Klippel-Trenaunay-Weber
/
Mancha Vino de Oporto
/
Síndromes Neurocutáneos
/
Extremidad Inferior
Tipo de estudio:
Estudio diagnóstico
Límite:
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Annals of Dermatology
Año:
2002
Tipo del documento:
Artículo
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