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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.
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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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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