TY - JOUR T1 - An Update on Clinicopathological, Imaging and Genetic Features of Desmoplastic Fibroblastoma (Collagenous Fibroma) JF - In Vivo JO - In Vivo SP - 69 LP - 73 DO - 10.21873/invivo.12233 VL - 35 IS - 1 AU - SHIZUHIDE NAKAYAMA AU - JUN NISHIO AU - MIKIKO AOKI AU - KAZUKI NABESHIMA AU - TAKUAKI YAMAMOTO Y1 - 2021/01/01 UR - http://iv.iiarjournals.org/content/35/1/69.abstract N2 - Desmoplastic fibroblastoma (also known as collagenous fibroma) is an uncommon benign fibroblastic/myofibroblastic neoplasm that primarily arises in the subcutaneous tissue of upper extremity. Magnetic resonance imaging reveals a well-defined mass in intimate association with dense connective tissue and prominent low signal intensity on all pulse sequences. Peripheral and septal enhancement is usually seen after intravenous contrast. Histologically, the lesion is paucicellular and consists of spindle to stellate-shaped cells embedded in a collagenous or myxocollagenous stroma with low vascularity. Diffuse and strong nuclear immunoreactivity for FOS-like antigen 1 seems to be characteristic of desmoplastic fibroblastoma. Cytogenetic studies have demonstrated the presence of 11q12 rearrangements and an identical t(2;11)(q31;q12) translocation. This review provides an updated overview of the clinical, radiological, histological, cytogenetic and molecular genetic features of desmoplastic fibroblastoma and discusses the relationship to fibroma of tendon sheath. ER -