A Case of Juvenile Xanthogranuloma Developed in a Neurofibromatosis Child with Family History / 대한피부과학회지
Korean Journal of Dermatology
;
: 547-549, 2008.
Artículo
en Coreano
| WPRIM
| ID: wpr-102059
ABSTRACT
Juvenile xanthogranuloma (JXG) is a fibrohistiocytic proliferative disorder predominant in infancy and childhood. It is a benign and transient skin lesion that usually appears in the cephalic area. Recently, the concurrent finding of neurofibromatosis (NF), juvenile chronic myelogenous leukemia (JCML), and JXG has been repeatedly reported. Especially, the family history of NF may represent a risk factor for the development of JCML in patients with NF and in patients with NF and JXG. So, a finding of JXG and NF in infants should alert the physician to a possible development of JCML. We report a case of JXG developed in a neurofibromatosis child with family history.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Piel
/
Factores de Riesgo
/
Xantogranuloma Juvenil
/
Neurofibromatosis
/
Leucemia Mielomonocítica Juvenil
Tipo de estudio:
Estudio de etiología
/
Factores de riesgo
Límite:
Niño
/
Humanos
/
Lactante
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
2008
Tipo del documento:
Artículo
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