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 3. (A) Masson stain showing green in the fibrotic areas, proving the collagen accumulation in ECM. (B) H&E staining shows benign fibroblastic cells with an eosinophilic ground substance in the background. (C) Showing positive immunohistochemical staining for collagen type VI in the extracellular matrix area (*). (D) Showing negative immunohistochemical staining for collagen type IV in patient’s biopsy tissue.