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. © 2010 by Korean Society of Otorhinolaryngology-Head and Neck Surgery.
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Park, K. T., Chang, D. Y., & Sung, M. W. (2010). Juvenile hyaline fibromatosis. Clinical and Experimental Otorhinolaryngology, 3(2), 102–106. https://doi.org/10.3342/ceo.2010.3.2.102
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