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

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. I...

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Veröffentlicht in:Revista portuguesa de estomatologia, medicina dentária e cirurgia maxilofacial medicina dentária e cirurgia maxilofacial, 2022-01, Vol.63 (2), p.99-104
Hauptverfasser: Amer, Hatem, Shaheen, Hamed, Ashoub, Madiha, Mahmoud, Sarah
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Sprache:eng
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Zusammenfassung: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.
ISSN:1646-2890
1647-6700
DOI:10.24873/j.rpemd.2022.06.867