26 June 2022>: Articles
Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
Challenging differential diagnosis, Rare disease, Congenital defects / diseases
Pongsakorn Choochuen A , Wison Laochareonsuk C , Pattama Tanaanantarak C , Kanet Kanjanapradit B , Surasak Sangkhathat A*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.