2005
DOI: 10.1016/j.surneu.2004.02.037
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Plexiform neurofibroma of the cauda equina: case report

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Cited by 5 publications
(6 citation statements)
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“…In our patient, the clinical manifestations were atypical because there were already symptoms due to poliomyelitis at childhood. In our case, consistent with 2 others, 6,7 the neoplasm was of mixed intensity on T1-and T2-weighted images. The intraoperative findings of tumor encompassing the nerves of the cauda equina are not typical of plexiform neurofibromas in this area.…”
Section: Discussionsupporting
confidence: 92%
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“…In our patient, the clinical manifestations were atypical because there were already symptoms due to poliomyelitis at childhood. In our case, consistent with 2 others, 6,7 the neoplasm was of mixed intensity on T1-and T2-weighted images. The intraoperative findings of tumor encompassing the nerves of the cauda equina are not typical of plexiform neurofibromas in this area.…”
Section: Discussionsupporting
confidence: 92%
“…Plexiform neurofibromas of the cauda equina are extremely rare tumors, with only 5 cases reported in the literature. [3][4][5][6][7] The ages of the affected patients ranged from 4 to 68 years. The neoplasm was a malignant plexiform neurofibroma in only 1 adult patient.…”
Section: Discussionmentioning
confidence: 99%
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“…It enlarges into a heterogeneous mass causing symptoms by compression or by engulfing other nerve elements [10]. The MRI reveals a lesion of mixed intensity on T1-and T2-weighted images, with diffuse heterogeneous enhancement on postcontrast images [10,26]. When the lesion is localized on a nerve, the intraoperative findings are usually of one or more thickened and elongated nerves, but not a mass distinct from the involved nerves [9].…”
Section: Neurofibromas: Backgroundmentioning
confidence: 99%
“…The treatment for neurofibromas is operative consisting of complete removal of the lesion by extensive surgical resection [9,26,28] to prevent or delay progression [11,26,28]. Postoperatively, in most of the patients the back pain improves, whereas the weakness and sensory loss remains [9].…”
Section: Neurofibromas: Backgroundmentioning
confidence: 99%