2014
DOI: 10.5334/jbr-btr.11
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Intraparenchymal meningioma in a child

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Cited by 6 publications
(10 citation statements)
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“…Other pathological patterns include: anaplastic, fibroblastic, meningothelial, transitional, sarcomatous, clear cell, chordoid, atypical, rhabdoid, papillary WHO III. 4 , 8 , 9 The pathological and differential diagnosis are chordoma, extraskeletal myxoid chondrosarcoma, low-grade chondrosarcoma, myxopapillary ependymoma, and chordoid glioma. 10 , 11 …”
Section: Discussionmentioning
confidence: 99%
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“…Other pathological patterns include: anaplastic, fibroblastic, meningothelial, transitional, sarcomatous, clear cell, chordoid, atypical, rhabdoid, papillary WHO III. 4 , 8 , 9 The pathological and differential diagnosis are chordoma, extraskeletal myxoid chondrosarcoma, low-grade chondrosarcoma, myxopapillary ependymoma, and chordoid glioma. 10 , 11 …”
Section: Discussionmentioning
confidence: 99%
“… 4 18 Furthermore, punctate calcification or overall tumor calcification can be found, but typically there is no mass effect or peritumoral edema. 4 6 , 8 , 12 , 13 , 15 In contrast-enhanced CT scanning, lesions of the parenchyma meningioma are significantly enhanced, and can present with homogeneous enhancement or no enhancement. 5 , 6 , 12 , 13 , 15 When using MRI, parenchyma meningiomas appear as a solid mass and hypointensity or equal signal strength is observed in T1WI lesions.…”
Section: Discussionmentioning
confidence: 99%
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“…Our review of the literature revealed fteen well-described cases of complete intraparenchymal meningioma. These mostly affected the cerebral hemispheres of patients aged between 14-month and 66-year-old [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16]. Only one case occurred in the medulla oblongata parenchyma, and was identi ed as meningothelial meningioma in 1985.…”
Section: Introductionmentioning
confidence: 99%