2018
DOI: 10.1016/j.ijscr.2017.12.019
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A case report of cervical neurofibrosarcoma: Clinical presentation, treatment and outcome

Abstract: HighlightsMalignant peripheral nerve sheath tumors are highly aggressive soft tissue sarcomas with poor prognosis.The recurrence rate is high.Complete surgical resection is the mainstay of therapy, when possible.

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Cited by 3 publications
(8 citation statements)
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References 14 publications
(15 reference statements)
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“…In the present series, there were only 2 cases over a 20-year period. Half of MPNSTs implicate degeneration of NF1 after 10-20 years' progression; the other half are de novo [18,19]. These literature data agree with the present findings.…”
Section: Malignant Peripheral Nerve Sheath Tumor (Mpnst)supporting
confidence: 92%
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“…In the present series, there were only 2 cases over a 20-year period. Half of MPNSTs implicate degeneration of NF1 after 10-20 years' progression; the other half are de novo [18,19]. These literature data agree with the present findings.…”
Section: Malignant Peripheral Nerve Sheath Tumor (Mpnst)supporting
confidence: 92%
“…Location is head and neck in about 10-15% of cases [18,19]. MPNST accounts for 10% of cervical sarcomas [19]. In the present series, there were only 2 cases over a 20-year period.…”
Section: Malignant Peripheral Nerve Sheath Tumor (Mpnst)mentioning
confidence: 45%
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“…Malignant neural sheath tumors of peripheral nerves comprise a group of neoplasms that can differentiate into various elements of the neural sheath, including Schwann cells, perineurial fibroblasts, and fibroblasts [1].…”
Section: Discussionmentioning
confidence: 99%