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Radiosurgical treatment of ulnar plexiform neurofibroma in a neurofibromatosis type 1 (NF1) patient

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Acknowledgments

The authors wish to thank Dr. David W. Schaal and Rose Tomey, Accuray Incorporated, for technical and editorial assistance.

Conflicts of interest

The authors hereby declare that no actual nor potential conflicts of interest exist. The authors have no financial interests in the instruments presented in this manuscript.

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No funding or financial support was received for this work.

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Correspondence to Marcello Marchetti.

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Comment

This is an interesting case report on a successful radiosurgical treatment for a recurrent neurofibroma of the extremities infiltrating the skin. Benign tumors respond very well to single-session radiosurgery. In this NF1 patient, the authors have chosen hypofractionation because of the tumor’s infiltration to the skin, which seems to have resulted in a rather high dose delivered to the skin if they had opted for a single-session regime. For genetic reasons, NF1- and NF2 patients have a high propensity for the development of neoplasms. Therefore, in these patients, a radiosurgical treatment for benign tumors of the extremities should only be a secondary treatment following open surgery whenever possible. In patients with a genetic predisposition for the development of tumors, it may also be prudent to use single-session regimes whenever possible in order to minimize radiation exposure. This report adds to the growing evidence of radiosurgery applied successfully to tumors of extracranial location.

Thomas Mindermann

Zurich, Switzerland

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Marchetti, M., Franzini, A., Nazzi, V. et al. Radiosurgical treatment of ulnar plexiform neurofibroma in a neurofibromatosis type 1 (NF1) patient. Acta Neurochir 155, 553–555 (2013). https://doi.org/10.1007/s00701-012-1597-5

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  • DOI: https://doi.org/10.1007/s00701-012-1597-5

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