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.
MeSH terms
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Accessory Nerve Diseases / etiology
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Cervical Vertebrae*
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Diathermy / methods
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Humans
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Infant
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Magnetic Resonance Imaging
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Male
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Myofibromatosis / diagnosis*
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Myofibromatosis / surgery
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Paralysis / etiology
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Postoperative Complications / etiology
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Soft Tissue Neoplasms / diagnosis*
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Soft Tissue Neoplasms / surgery
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Spinal Neoplasms / diagnosis