26 June 2022
: Case report 
Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
Challenging differential diagnosis, Rare disease, Congenital defects / diseases
Pongsakorn Choochuen1ABCDEF, Wison Laochareonsuk12CD, Pattama Tanaanantarak3CD, Kanet Kanjanapradit4B, Surasak Sangkhathat25ADEG*DOI: 10.12659/AJCR.935921
Am J Case Rep 2022; 23:e935921
Figure 2. CT of the head of the patient, transverse plane (A) and coronal plane (B), showing multiple well-defined enhanced soft-tissue masses at the scalp, varying in size, with the largest one about 6.3 cm in diameter at the occipital region. The lower skull shows no cortical destruction, periosteal reaction, or sclerotic change.