A Case of Juvenile Xanthogranuloma Developed in a Neurofibromatosis Child with Family History / 대한피부과학회지
Korean Journal of Dermatology
;
: 547-549, 2008.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Peau
/
Facteurs de risque
/
Xanthome juvénile
/
Neurofibromatoses
/
Leucémie myélomonocytaire juvénile
Type d'étude:
Etude d'étiologie
/
Facteurs de risque
Limites du sujet:
Enfant
/
Humains
/
Bébé
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
2008
Type:
Article
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