| Literature DB >> 26682835 |
Priyadharshini Rajendran1, Balaganesh Karmegaraj2, Mukul Vij3, Julius Xavier Scott4.
Abstract
Juvenile hyaline fibromatosis (JHF) is a rare progressive autosomal recessive disease that is characterised by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present an 18-month-old boy with JHF. This case demonstrates that JHF should be considered in the differential diagnosis when multiple subcutaneous nodules are observed in the face, head and neck. Gum hypertrophy with palatal nodules is unusual in JHF. 2015 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2015 PMID: 26682835 PMCID: PMC4691940 DOI: 10.1136/bcr-2015-211506
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X