| Literature DB >> 10486019 |
S Imaizumi1, A Ogose, T Hotta, H E Takahashi, I Emura.
Abstract
A rare case of solitary infantile myofibromatosis of bone is reported in the right clavicle of a 15-year-old boy. A radiograph demonstrated an osteolytic lesion with a sharp margin and a sclerotic rim. CT revealed a circumscribed lesion with slight expansion of the cortex. On MRI the lesion appeared isointense to muscle on T1-weighted images, bright on T2-weighted images, and showed marked gadolinium enhancement. The patient was well, without evidence of recurrence or metastasis, 4 years and 5 months following resection.Entities:
Mesh:
Year: 1999 PMID: 10486019 DOI: 10.1007/s002560050550
Source DB: PubMed Journal: Skeletal Radiol ISSN: 0364-2348 Impact factor: 2.199