A Case of Juvenile Xanthogranuloma Developed in a Neurofibromatosis Child with Family History / 대한피부과학회지
Korean Journal of Dermatology
;
: 547-549, 2008.
Artigo
em 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:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pele
/
Fatores de Risco
/
Xantogranuloma Juvenil
/
Neurofibromatoses
/
Leucemia Mielomonocítica Juvenil
Tipo de estudo:
Estudo de etiologia
/
Fatores de risco
Limite:
Criança
/
Humanos
/
Lactente
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2008
Tipo de documento:
Artigo
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