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  • Title: Solitary infantile myofibromatosis involving the clavicle.
    Author: Imaizumi S, Ogose A, Hotta T, Takahashi HE, Emura I.
    Journal: Skeletal Radiol; 1999 Aug; 28(8):473-6. PubMed ID: 10486019.
    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.
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