World Journal of Surgical Oncology (Jan 2005)

Resection of small plexiform neurofibromas in neurofibromatosis type 1 children

  • Fünsterer Carsten,
  • Hartmann Melanie,
  • Schmelzle Rainer,
  • Friedrich Reinhard E,
  • Mautner Victor-F

DOI
https://doi.org/10.1186/1477-7819-3-6
Journal volume & issue
Vol. 3, no. 1
p. 6

Abstract

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Abstract Background Plexiform neurofibromas (PNF) are benign tumors of the peripheral nerve which mostly develop in patients with neurofibromatosis type 1 (NF1). Surgical interventions are usually not applied to children with small tumors. These are rather restricted to debulking of larger tumors in adults that cause clinical complications or aesthetic disfigurement. In most cases, a total resection of PNF is not possible due to the network-like growth of the tumors. Patients and methods Early surgical intervention was carried out for 9 small PNFs in 7 NF1 children. Tumor resection was performed following the graphical delineation of the affected skin and according the MRI findings. Results Total resection was achieved for all 9 PNF without causing any neurological or organic deficit. Annual magnetic resonance tomography over a period of four years did not reveal any relapse of the tumors. Conclusions Early surgical intervention for small superficial PNFs in NF1 children have various advantages and may especially be considered a strategy to prevent progression.