2022
DOI: 10.1016/j.wneu.2022.04.135
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Primary Benign Tumors of the Spinal Canal

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Cited by 13 publications
(6 citation statements)
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“…NF1 causes tumors along the nervous system which can present as intraspinal or paraspinal tumors or in combination; they are noted in more than one-third of patients with NF1. 68 , 70 , 71 They are isolated neurofibromas or plexiform neurofibromas (with the incidence of 25%–50%). 69 Plexiform neurofibromas may be followed by pain, neurologic deficits, and deformity of adjacent structures.…”
Section: Tumorsmentioning
confidence: 99%
“…NF1 causes tumors along the nervous system which can present as intraspinal or paraspinal tumors or in combination; they are noted in more than one-third of patients with NF1. 68 , 70 , 71 They are isolated neurofibromas or plexiform neurofibromas (with the incidence of 25%–50%). 69 Plexiform neurofibromas may be followed by pain, neurologic deficits, and deformity of adjacent structures.…”
Section: Tumorsmentioning
confidence: 99%
“…Malignant Schwann cell-derived tumors are rare and classified as malignant nerve sheath tumors (MNST) according to the WHO classification of 2016 [3,4]. Spinal schwannomas account for approximately 25% of all intradural spinal cord tumors [3,[5][6][7], with an incidence of 0.3-0.7 per 100,000 person years [8]. Tumors may be both intra-and extradural and may extend through the neural foramen to develop an hourglass or dumbbell shape [9].…”
Section: Introductionmentioning
confidence: 99%
“…Schwannomas are WHO grade 1 nerve sheath tumors that may affect peripheral, spinal, or cranial nerves [1][2][3][4]. Spinal schwannomas comprise 25% of all intradural spinal cord tumors [2,5,6] with an incidence of 0.3-0.7 per 100,000 [7]. Although benign, large schwannomas can compress nerve roots or the spinal cord, resulting in neurological deficits.…”
Section: Introductionmentioning
confidence: 99%