Juvenile Hyaline Fibromatosis
Clinical and Experimental Otorhinolaryngology
;
: 102-106, 2010.
Article
Dans Anglais
| WPRIM
| ID: wpr-205383
ABSTRACT
Juvenile hyaline fibromatosis (JHF) is a rare, progressive autosomal recessive disease that's characterized by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present here the case of a 2-yr-old boy with JHF along with a review of the relevant literature. This case demonstrates that JHF should be considered in the differential diagnosis when multiple subcutaneous nodules are observed in the face, head and neck.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Peau
/
Contracture
/
Diagnostic différentiel
/
Hyalinose systémique
/
Fibrome
/
Gencive
/
Hypertrophie gingivale
/
Tête
/
Substance hyaline
/
Articulations
Type d'étude:
Etude diagnostique
langue:
Anglais
Texte intégral:
Clinical and Experimental Otorhinolaryngology
Année:
2010
Type:
Article
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