Revista Portuguesa de Estomatologia, Medicina Dentária e Cirurgia Maxilofacial (Jun 2022)

Malignant peripheral nerve sheath tumor with rhabdoid features arising in the temporal region of a patient suffering from neurofibromatosis 1 – A case report

  • Hatem Wael Amer,
  • Hamed Abdelwahab Shaheen,
  • Madiha Nabil Ashoub,
  • Sarah Ahmed Mohamed Mahmoud

DOI
https://doi.org/10.24873/j.rpemd.2022.06.867
Journal volume & issue
Vol. 63, no. 2
pp. 99 – 104

Abstract

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The malignant peripheral nerve sheath tumor is one of the rare sarcomas that have a challenging diagnosis. It occurs independently with neurofibromatosis type 1. Some studies referred that malignant peripheral nerve sheath tumor attains a worse prognosis when it occurs in the head and neck region. In the reported case, a male patient with neurofibromatosis type 1 manifestations presented with a large mass in the temporal region. Based on the clinical history, histopathology, and immunohistochemical findings, the lesion was diagnosed as a low-grade malignant peripheral nerve sheath tumor with rhabdoid features. Surgical resection followed by intensity-modulated radiotherapy was the treatment of choice.

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