This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Myofibroma is a rare benign neoplasm of myofibroblastic cells that can occur in either a so...

Chest radiography, CT, and MR imaging were performed in a 3-year-old girl who had posterior mediastinal fibromatosis with transforaminal intraspinal and chest wall extension. Chest radiographs and CT scans showed a slow-growing, noncalcified but locally aggressive left paravertebral mass. The mass was slightly hyperintense relative to muscle on both T1-weighted and fast spin-echo T2-weighted MR...

Citation: Newaz ZA, Pannu V, Kennedy J, Barghan S, Kashtwari DN, et al. (2015) Imaging Features of Intraosseous Myofibroma of the Jaws: A Case Report and Literature Review. J Adv Radiol Med Image 1(1): 102 Volume 1 | Issue 1 Journal of Advances in Radiology and Medical Imaging Introduction The terminology regarding myofibroma has historically had some variation and confusion. Older terms report...

Ultimate widespread use of CGF entities in tactical simulations will depend on how easy it will be to develop, refine and maintain models of the behaviors to be represented. However, proper vehicle behavior model development for CGF applications can be difficult as well as expensive. Means to quickly and effectively create models for new vehicles and/or behaviors must be developed to permit CGF...

The present case report describes a case of infantile myofibromatosis (IM) with a pseudo-ulcerated plaque on the right side of the back of a fetus, detected in the 38th week of gestation using prenatal ultrasound. The fetus was examined weekly by ultrasound to measure the size of the mass. At birth, the scarlet mass was slightly elevated compared with the skin around it, with a cavity in the ce...

Notch signaling regulates a vast array of crucial developmental processes. It is therefore not surprising that mutations in genes encoding Notch receptors or ligands lead to a variety of congenital disorders in humans. For example, loss of function of Notch results in Adams-Oliver syndrome, Alagille syndrome, spondylocostal dysostosis and congenital heart disorders, while Notch gain of function...