Juvenile Hyaline Fibromatosis
Clinical and Experimental Otorhinolaryngology
;
: 102-106, 2010.
Article
in English
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Skin
/
Contracture
/
Diagnosis, Differential
/
Hyaline Fibromatosis Syndrome
/
Fibroma
/
Gingiva
/
Gingival Hypertrophy
/
Head
/
Hyalin
/
Joints
Type of study:
Diagnostic study
Language:
English
Journal:
Clinical and Experimental Otorhinolaryngology
Year:
2010
Type:
Article
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