Juvenile Hyaline Fibromatosis
Clinical and Experimental Otorhinolaryngology
;
: 102-106, 2010.
Artigo
em Inglês
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pele
/
Contratura
/
Diagnóstico Diferencial
/
Síndrome da Fibromatose Hialina
/
Fibroma
/
Gengiva
/
Hipertrofia Gengival
/
Cabeça
/
Hialina
/
Articulações
Tipo de estudo:
Estudo diagnóstico
Idioma:
Inglês
Revista:
Clinical and Experimental Otorhinolaryngology
Ano de publicação:
2010
Tipo de documento:
Artigo
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