nerve

(redirected from Nerve sheath tumor)
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Related to Nerve sheath tumor: neurofibromatosis
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Synonyms for nerve

tension

get on someone's nerves

Synonyms

nerve yourself

Synonyms

  • brace yourself
  • prepare yourself
  • steel yourself
  • fortify yourself
  • gear yourself up
  • gee yourself up

Synonyms for nerve

Synonyms for nerve

References in periodicals archive ?
Malignant peripheral nerve sheath tumor in the anterior skull base associated with neurofibromatosis type 1.
24) TLE1 positivity is seen in 85% to 97% of synovial sarcomas; however, it has also been reported in endometrial stromal sarcoma, SFT, malignant peripheral nerve sheath tumor, Ewing sarcoma, schwannoma, and epithelioid sarcoma.
Malignant peripheral nerve sheath tumor of the lower labial mucosa: case report and literature review.
Peripheral nerve sheath tumor in a subadult golden eagle (Aquila chrysaetos).
The report provides a snapshot of the global therapeutic landscape of Peripheral Nerve Sheath Tumor (Neurofibrosarcoma)
Gebhardt, "Malignant peripheral nerve sheath tumors (MPNSTs)," Electronic Sarcoma Update Newsletter, vol.
5) Finally, druggable mutations that are known to be common in certain tumor types may also be common in others; for example, BRAF mutations, commonly associated with melanoma, have now been reported in malignant peripheral nerve sheath tumors and are associated with response to vemurafinib.
A neurofibroma is a benign nerve sheath tumor of Schwann cell origin.
Neurofibromatosis type 1 revealed by malignant peripheral nerve sheath tumor.
Schwannoma is a benign nerve sheath tumor originating from the normal peripheral nerve, which is composed of neoplastic cells demonstrating features of constituent Schwann cells of the normal peripheral nerve sheath.
The first category includes traumatic neuroma, neurofibroma, neurilemmoma, and palisaded encapsulated neuroma (PEN) whereas the second category consists of malignant peripheral nerve sheath tumor (MPNST).
Malignant peripheral nerve sheath tumor (MPNST) was ranked as the most important manifestation to treat by the highest percentage of patients (39%) and achieved the highest average rank (2.
NF1 patients with neurofibromas have a 10% lifetime risk of developing a malignant peripheral nerve sheath tumor within one of the lesions.
The differential diagnosis is fairly broad and includes phlegmon/abscess, nerve sheath tumor, synovial sarcoma, fibrous histiocytoma (benign, malignant and angiomatoid forms), angiosarcoma, and fibromatosis.