Juvenile Hyaline Fibromatosis
Clinical and Experimental Otorhinolaryngology
; : 102-106, 2010.
Article
en En
| WPRIM
| ID: wpr-205383
Biblioteca responsable:
WPRO
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.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Piel
/
Contractura
/
Diagnóstico Diferencial
/
Síndrome de Fibromatosis Hialina
/
Fibroma
/
Encía
/
Hipertrofia Gingival
/
Cabeza
/
Hialina
/
Articulaciones
Tipo de estudio:
Diagnostic_studies
Idioma:
En
Revista:
Clinical and Experimental Otorhinolaryngology
Año:
2010
Tipo del documento:
Article