Challenging Management of Plexiform Schwannoma and Plexiform Neurofibroma

J Craniofac Surg. 2022 May 1;33(3):803-808. doi: 10.1097/SCS.0000000000008381. Epub 2021 Dec 2.

Abstract

Plexiform variants of neurofibromas and schwannomas are rare and typically arise in superficial soft tissues in the head and neck region. The treatment of these tumors is challenging and no generally accepted guidelines exist for their optimal management. The purpose of this study was to review the management and longterm prognosis of head and neck plexiform neurofibromas and schwannomas at 2 tertiary care academic hospitals in Finland over a 31-year period. The pathology files were searched for plexiform neurofibromas and schwannomas between the years 1990 and 2020. The case notes were reviewed for full management details. Two plexiform schwannomas and 6 plexiform neurofibromas were identified. Five of the 6 plexiform neurofibromas were managed operatively. All patients with a surgically managed plexiform neurofibroma underwent multiple operations. Sclerotherapy abolished 1 patient's cutaneous plexiform neurofibromas. The management of plexiform neurofibromas and plexiform schwannomas remains challenging. Sclerotherapy may offer a promising management option for cutaneous plexiform neurofibromas.

MeSH terms

  • Head and Neck Neoplasms* / surgery
  • Humans
  • Neurilemmoma* / surgery
  • Neurofibroma, Plexiform* / surgery
  • Prognosis