Bibliografie tematiche / Chordoid Glioma

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Letteratura scientifica selezionata sul tema "Chordoid Glioma"

Autore: Grafiati
Pubblicato: 16 novembre 2024
Ultima modifica: 31 luglio 2025

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Articoli di riviste sul tema "Chordoid Glioma"

1

Thavaratnam, LK, ST Loy, A. Gupta, I. Ng, and JF Cullen. "Chordoid glioma." Singapore Medical Journal 56, no. 11 (2015): 641–43. http://dx.doi.org/10.11622/smedj.2015175.

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2

Liu, Wei-ping, Jin-xiang Cheng, Xi-cai Yi, et al. "Chordoid Glioma." Neurologist 17, no. 1 (2011): 52–56. http://dx.doi.org/10.1097/nrl.0b013e3181e7db67.

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3

Leeds, Norman E., Frederick F. Lang, Teresa Ribalta, Raymond Sawaya, and Gregory N. Fuller. "Origin of Chordoid Glioma of the Third Ventricle." Archives of Pathology & Laboratory Medicine 130, no. 4 (2006): 460–64. http://dx.doi.org/10.5858/2006-130-460-oocgot.

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Abstract (sommario):
Abstract Context.—Chordoid glioma is a relatively recently described unique glial neoplasm that has been formally codified by the World Health Organization in Pathology and Genetics of Tumours of the Nervous System, in which it is included along with astroblastoma and gliomatosis cerebri under the rubric “Tumors of Uncertain Origin.” Many examples of chordoid glioma come to clinical attention only at a relatively large size and occupy a large portion of the third ventricle. Accordingly, the anatomic origin of chordoid glioma has been unclear and debated. Objective.—To examine the regional anat
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4

Ricoy, J. R., R. D. Lobato, B. Báez, A. Cabello, M. A. Martínez, and G. Rodríguez. "Suprasellar chordoid glioma." Acta Neuropathologica 99, no. 6 (2000): 699–703. http://dx.doi.org/10.1007/s004010051183.

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5

Brat, D. J., B. W. Scheithauer, S. C. Cortez, K. Brecher, and P. C. Burger. "THIRD VENTRICULAR “CHORDOID GLIOMA”." Journal of Neuropathology and Experimental Neurology 56, no. 5 (1997): 586. http://dx.doi.org/10.1097/00005072-199705000-00072.

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Brat, Daniel J. "Chordoid glioma further defined." Advances in Anatomic Pathology 9, no. 1 (2002): 77. http://dx.doi.org/10.1097/00125480-200201000-00016.

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Buccoliero, Anna Maria, Adele Caldarella, Pasquale Gallina, Nicola Di Lorenzo, Antonio Taddei, and Gian Luigi Taddei. "Chordoid Glioma: Clinicopathologic Profile and Differential Diagnosis of an Uncommon Tumor." Archives of Pathology & Laboratory Medicine 128, no. 11 (2004): e141-e145. http://dx.doi.org/10.5858/2004-128-e141-cgcpad.

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Abstract (sommario):
Abstract Chordoid glioma is an uncommon low-grade brain neoplasm arising in the third ventricular region, predominantly in middle-aged women. It characteristically shows chordoma-like histologic features and glial fibrillary acidic protein immunoreactivity. We present a case of chordoid glioma in a previously healthy 56-year-old woman admitted to our hospital because of a cranial trauma subsequent to an incidental fall. Radiologic examinations revealed a well-demarcated, partially cystic, enhancing mass at the level of the lamina terminalis. The lesion was surgically removed. The patient remai
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Sanda, Nicolae, Claudiu-Nicolae Mircea, Michèle Bernier, Avinoam B. Safran, and Sorin Aldea. "Chordoid Glioma Infiltrating Optic Structures." Journal of Neuro-Ophthalmology 39, no. 3 (2019): 408–10. http://dx.doi.org/10.1097/wno.0000000000000757.

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Castellano-Sanchez, Amilcar Antonio, Erwin Schemankewitz, Claire Mazewski, and Daniel J. Brat. "Pediatric Chordoid Glioma withChondroid Metaplasia." Pediatric and Developmental Pathology 4, no. 6 (2001): 564–67. http://dx.doi.org/10.1007/s10024001-0087-1.

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Brat, Daniel J. "The Elusive Origin of Chordoid Glioma." Archives of Pathology & Laboratory Medicine 130, no. 4 (2006): 437–38. http://dx.doi.org/10.5858/2006-130-437-teoocg.

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Più fonti

Tesi sul tema "Chordoid Glioma"

1

Bellamy, Charlotte. "Functional characterization of a novel mutation in PRKCA, the major driver of Chordoid glioma." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASL052.

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Abstract (sommario):
Le gliome chordoïde (ChG) est une tumeur cérébrale rare de bas grade, caractérisée par une nouvelle mutation ponctuelle récurrente PRKCA p.D463H, une substitution dans le domaine kinase de la protéine kinase C alpha (PKCα). Cette étude démontre le rôle de cette kinase mutée dans le développement des ChG. Ici, nous montrons l'inactivation et l'effet négatif dominant de PKCαD463H via des tests d'activité in vitro et in cellulo. Nos résultats montrent que la mutation affecte la structure tertiaire, ce qui entraîne une protéine ouverte et instable. Les données de spectrométrie de masse phosphoprot
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Libri sul tema "Chordoid Glioma"

1

van den Bent, Martin J., Frederic Dhermain, and Walter Stummer. Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0007.

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Abstract (sommario):
This chapter contains a description of three rare entities: astroblastoma, angiocentric glioma, and chordoid glioma. Because these tumours are so rare, the evidence on how to best treat them is anecdotal and essentially consists of case series, but it is the best guidance available and the presentation of larger series with new cases remain unlikely. If one is confronted with such a case, a meticulous review of the clinical, radiological, and pathological characteristics of the case is indicated, to minimize the risk of an erroneous diagnosis. If the case does not fit in with the descriptions
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Capitoli di libri sul tema "Chordoid Glioma"

1

Liu, Dongyou. "Chordoid Glioma, Angiocentric Glioma, and Diffuse Midline Glioma." In Tumors and Cancers. CRC Press, 2017. http://dx.doi.org/10.1201/9781315120522-6.

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2

"Chordoid Glioma of 3rd Ventricle." In Diagnostic Pathology: Neuropathology. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-44592-4.50027-5.

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"Chordoid Glioma of the Third Ventricle." In Diagnostic Imaging: Brain. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37754-6.50140-8.

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4

Gallia, Gary L., Martin G. Pomper, and Alessandro Olivi. "Chordoid Glioma of the Third Ventricle." In Textbook of Neuro-Oncology. Elsevier, 2005. http://dx.doi.org/10.1016/b978-0-7216-8148-1.50032-2.

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5

Brat, Daniel. "Chordoid glioma of the third ventricle." In Russell & Rubinstein's Pathology of Tumors of the Nervous System 7Ed. CRC Press, 2006. http://dx.doi.org/10.1201/b13439-17.

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6

Filbin, Mariella, Sanda Alexandrescu, Daphne Haas-Kogan, Ian F. Pollack, David A. Reardon, and Christine Haberler. "Circumscribed astrocytic gliomas." In Oxford Textbook of Neuro-Oncology, 2nd ed., edited by Tracy Batchelor and Michael Weller. Oxford University PressOxford, 2025. https://doi.org/10.1093/med/9780198869702.003.0009.

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Abstract (sommario):
Abstract Pilocytic astrocytoma is a slow-growing tumor occurring in children and corresponds to World Health Organization grade 1. It is characterized by MAPK pathway alterations and prognosis is very good. High-grade astrocytoma with piloid features occurs in adults, shows signs of anaplasia, MAPK pathway alterations, and distinct DNA methylation. Pleomorphic xanthoastrocytoma occurs in children and young adults with BRAF V600E mutations, homozygous CDKN2A/CDKN2B deletions, and is assigned grade 2 or 3. Chordoid glioma is a rare, slow-growing glioma occurring in adults, and is characterized b
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