| Literature DB >> 18661320 |
A K Sinha1, E C Jesudason, C L Mallucci, P D Losty, G Kokai, B L Pizer.
Abstract
Infantile myofibromatosis (IM) is a rare pathological entity characterized by solitary or multiple nodular skin, soft tissues or bony lesions. Craniovertebral (CV) junction lesions are rare. We report the successful management of a solitary IM involving the posterior elements of the CV junction in a 6-month-old child.Entities:
Mesh：
Year: 2008 PMID： 18661320 DOI： 10.1080/02688690701882022
Source DB: PubMed Journal: Br J Neurosurg ISSN： 0268-8697 Impact factor: 1.596