Skip to main content

Advertisement

Log in

Solitary infantile myofibromatosis involving the clavicle

  • Case Report
  • Published:
Skeletal Radiology Aims and scope Submit manuscript

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 11 August 1998 Revision requested: 5 October 1998, 18 March 1999 Revision received: 15 March 1999, 23 April 1999 Accepted: 28 April 1999

Rights and permissions

Reprints and permissions

About this article

Cite this article

Imaizumi, S., Ogose, A., Hotta, T. et al. Solitary infantile myofibromatosis involving the clavicle. Skeletal Radiol 28, 473–476 (1999). https://doi.org/10.1007/s002560050550

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s002560050550

Navigation