Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis): whole-body MR findings in two siblings with different subcutaneous nodules distribution.
Davide CastiglioneMaria Chiara TerranovaDario PiconeGiuseppe Lo ReSergio SalernoPublished in: Skeletal radiology (2017)
Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis) is a rare, progressive, autosomal recessive disorder whose main hallmark is the deposition of amorphous hyaline material in soft tissues, with an evolutionary course and health impairment. It may present involvement of subcutaneous or periskeletal soft tissue, or may develop as a visceral infiltration entity with poor prognosis. Very few radiological data about this inherited condition have been reported, due to the extreme rarity of disease. We herein present a case of two siblings, affected by different severity of the disease, with different clinical features. They were examined by whole-body MR (WBMR) in order to assess different lesions localization, to rule out any visceral involvement and any other associated anomalies and to define patients' management.
Keyphrases
- poor prognosis
- intellectual disability
- end stage renal disease
- long non coding rna
- soft tissue
- ejection fraction
- magnetic resonance
- healthcare
- insulin resistance
- chronic kidney disease
- newly diagnosed
- multiple sclerosis
- public health
- gene expression
- prognostic factors
- contrast enhanced
- peritoneal dialysis
- case report
- climate change
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- electronic health record
- magnetic resonance imaging
- computed tomography
- machine learning
- autism spectrum disorder
- adipose tissue
- deep learning
- human health