Imaizumi S, Ogose A, Hotta T, Takahashi H E, Emura I
Department of Orthopedic Surgery, Niigata University School of Medicine, Asahimachidouri 1-757 Niigata City, Niigata, Japan 951-8510, USA.
Skeletal Radiol. 1999 Aug;28(8):473-6. doi: 10.1007/s002560050550.
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.