"T1: heterogeneous, mostly isointense signal intensity"
"T2: heterogeneous iso- to high signal intensity"
"T1 C+ (Gd): discrete enhancement "
"Juvenile hyaline fibromatosis is a very rare disorder in infancy and childhood. It follows an autosomal recessive inheritance pattern and does not have any gender predominance 1."
"The diagnosis of juvenile hyaline fibromatosis is established by a combination of clinical and pathological features 1."
"The diagnosis of juvenile hyaline fibromatosis is established by a combination of clinical and pathological features 1."
"T1: heterogeneous, mostly isointense signal intensity"
"T2: heterogeneous iso- to high signal intensity"
"T1 C+ (Gd): discrete enhancement "
"T1 C+ (Gd): discrete enhancement "
"loss of ANTXR2 function confirmed by germline sequencing"
"Gene mutations affect the ANTXR2 (CMG2) gene on chromosome 4q21."
"Hyaline is diastase resistant and strongly positive for PAS, which is a special stain and not an immunostain 1."
Expected headings
"Associations"
"Signal characteristics"
"There are only a few reports in the literature focussing on imaging appearances of juvenile hyaline fibromatosis. The disease is characterised by subcutaneous or cutaneous nodules. Osseous involvement causes osteolytic lesions, which might be found in the skull, the long bones and phalanges of the hands and feet 2-4."