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Juvenile hyaline fibromatosis: focus on radiographic features in adulthood.
Slimani, Samy; Haddouche, Assia; Haid, Sabrina; Ladjouze-Rezig, Aicha.
Affiliation
  • Slimani S; Department of Rheumatology, Ben Aknoun Hospital, Algiers, 16300, Algeria. slimani@dr.com
Rheumatol Int ; 31(2): 273-6, 2011 Feb.
Article in En | MEDLINE | ID: mdl-20661739
ABSTRACT
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive hereditary disorder (less than 80 cases reported), characterized by multiple nodular lesions on the skin and musculoskeletal involvement, very debilitating because most adolescents and adults become bedridden. Only 10 cases have been reported on JHF in adulthood. We report the case of a 34-year-old male patient in whom clinical and histological findings were consistent with a mild JHF and focus on the radiographic features. The main purpose of this report is to increase the information available related to the radiographic manifestations and prognosis of JHF.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyaline Fibromatosis Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Rheumatol Int Year: 2011 Document type: Article Affiliation country: Algeria

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyaline Fibromatosis Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Rheumatol Int Year: 2011 Document type: Article Affiliation country: Algeria