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Zeitschriftenartikel zum Thema „Gliomes Chordoides“

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Veröffentlicht am 16. November 2024

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1

Leeds, Norman E., Frederick F. Lang, Teresa Ribalta, Raymond Sawaya und Gregory N. Fuller. „Origin of Chordoid Glioma of the Third Ventricle“. Archives of Pathology & Laboratory Medicine 130, Nr. 4 (01.04.2006): 460–64. http://dx.doi.org/10.5858/2006-130-460-oocgot.

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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 anatomic origin of chordoid glioma. Data Sources.—The clinical, imaging, histologic, immunophenotypic, and ultrastructural data in previously published case series and individual case reports of chordoid glioma were reviewed in conjunction with the study of a new case of chordoid glioma that presented at a relatively small size, thereby facilitating neuroanatomic localization. Conclusions.—Chordoid glioma exhibits features of specialized ependymal differentiation on ultrastructural examination, and all examples reported in the literature to date have displayed a highly stereotypical suprasellar anatomic localization and an ovoid shape, as seen on neuroimaging studies and gross anatomy. Neuroanatomic, radiologic, and clinical evidence supports an anatomic origin for chordoid glioma from the vicinity of the lamina terminalis.

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2

Thavaratnam, LK, ST Loy, A. Gupta, I. Ng und JF Cullen. „Chordoid glioma“. Singapore Medical Journal 56, Nr. 11 (November 2015): 641–43. http://dx.doi.org/10.11622/smedj.2015175.

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3

Liu, Wei-ping, Jin-xiang Cheng, Xi-cai Yi, Hai-ning Zhen, Zhou Fei, Qing Li und Xiang Zhang. „Chordoid Glioma“. Neurologist 17, Nr. 1 (Januar 2011): 52–56. http://dx.doi.org/10.1097/nrl.0b013e3181e7db67.

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4

Ricoy, J. R., R. D. Lobato, B. Báez, A. Cabello, M. A. Martínez und G. Rodríguez. „Suprasellar chordoid glioma“. Acta Neuropathologica 99, Nr. 6 (09.06.2000): 699–703. http://dx.doi.org/10.1007/s004010051183.

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5

Konovalov, A. N., I. V. Chernov, M. V. Ryzhova, D. I. Pitskhelauri, Yu V. Kushel, L. I. Astafieva, O. I. Sharipov et al. „Chordoid gliomas of the third ventricle“. Voprosy neirokhirurgii imeni N.N. Burdenko 87, Nr. 6 (2023): 14. http://dx.doi.org/10.17116/neiro20238706114.

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6

Brat, D. J., B. W. Scheithauer, S. C. Cortez, K. Brecher und P. C. Burger. „THIRD VENTRICULAR “CHORDOID GLIOMA”“. Journal of Neuropathology and Experimental Neurology 56, Nr. 5 (Mai 1997): 586. http://dx.doi.org/10.1097/00005072-199705000-00072.

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7

Brat, Daniel J. „Chordoid glioma further defined“. Advances in Anatomic Pathology 9, Nr. 1 (Januar 2002): 77. http://dx.doi.org/10.1097/00125480-200201000-00016.

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8

Suetens, Kristin, Jeroen Swinnen, Linde Stessens, Sofie Van Cauter und Geert Gelin. „Chordoid Glioma as a Differential Diagnosis of Anterior Third Ventricle Tumours: A Rare Case Report and Five-Year Follow-Up“. Case Reports in Radiology 2019 (04.12.2019): 1–6. http://dx.doi.org/10.1155/2019/3584837.

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Chordoid glioma is a rare and relatively recently defined tumour entity. Worldwide there have only been around 90 cases described until now. A chordoid glioma comprises a low-grade suprasellar neuroepithelial neoplasm originating in the anterior part of the third ventricle, with consistent radiological features on MRI. This lesion should be considered as a differential of third ventricle tumours. The patient described in this paper is quite unique in the sense that despite only partial tumour resection was obtained, the residual tumour was not progressive during several years of follow-up. Preoperative recognition of this disease entity is crucial to modify the treatment approach and improve patient outcome.

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9

Bellamy, Charlotte, Hannah Tovell, Florent Dingli, Damarys Loew, Stephane Liva, Selina Schwaighofer, Eduard Stefan, Alexandra Newton, Marc Sanson und Franck Bielle. „Abstract 4370: Functional characterisation of a novel mutation in PRKCA, a major driver of chordoid gliomas“. Cancer Research 84, Nr. 6_Supplement (22.03.2024): 4370. http://dx.doi.org/10.1158/1538-7445.am2024-4370.

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Abstract Chordoid gliomas (ChG) are a rare low-grade brain tumor, believed to be derived from tanycytes. An analysis by the team identified a novel mutation present in all ChGs: PRKCA p.D463H. This mutation involves a D463H substitution at the kinase domain of the Protein kinase C alpha (PKCα), it is not found in any other cancer, and represents the hallmark of ChG. The aim of the project is to identify novel and biologically relevant PKCαD463H signaling pathways, which will demonstrate the involvement and the role of this mutated kinase in cellular functions implicated in the development of ChGs. The D463H mutation affects a critical residue of the kinase domain of PKCα, suggesting that such a change modifies substrate affinity. Following the purification of PKCαD463H, we have shown its inactivation via in vitro kinase assays and peptide array. In cellulo fret-based activity reporter assays have shown that PKCαD463H has a dominant negative effect over PKCαWT. Through co-immunoprecipitation we have shown that the mutant protein can bind the WT form and also colocalizes in the cell. Our results also show that the mutation affects the tertiary structure of the protein, resulting in a more open, unstable protein compared to the WT. Phosphoproteomic analysis of HEK cells overexpressing PKC⍺D463H show a decrease of phosphorylation specifically on proteins involved with cell-cell adhesion, including functionally relevant phosphosites. This is in line with our Co-IP mass spectrometry data which shows a decrease in interaction of PKC⍺D463H with proteins involved in cell junctions. The cell of origin, tanycytes, are highly specialized cells that contain important cell-cell junctions and therefore their perturbation could be a potential route of tumorigenesis. By understanding these changes integrated with our snRNAseq and bulk RNAseq of ChGs, and exploration in cellular models, we hope to elucidate the mechanism by which the mutation leads to the development of Chordoid Glioma. Citation Format: Charlotte Bellamy, Hannah Tovell, Florent Dingli, Damarys Loew, Stephane Liva, Selina Schwaighofer, Eduard Stefan, Alexandra Newton, Marc Sanson, Franck Bielle. Functional characterisation of a novel mutation in PRKCA, a major driver of chordoid gliomas [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 4370.

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10

Sanda, Nicolae, Claudiu-Nicolae Mircea, Michèle Bernier, Avinoam B. Safran und Sorin Aldea. „Chordoid Glioma Infiltrating Optic Structures“. Journal of Neuro-Ophthalmology 39, Nr. 3 (September 2019): 408–10. http://dx.doi.org/10.1097/wno.0000000000000757.

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11

Castellano-Sanchez, Amilcar Antonio, Erwin Schemankewitz, Claire Mazewski und Daniel J. Brat. „Pediatric Chordoid Glioma withChondroid Metaplasia“. Pediatric and Developmental Pathology 4, Nr. 6 (01.11.2001): 564–67. http://dx.doi.org/10.1007/s10024001-0087-1.

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12

Brat, Daniel J. „The Elusive Origin of Chordoid Glioma“. Archives of Pathology & Laboratory Medicine 130, Nr. 4 (01.04.2006): 437–38. http://dx.doi.org/10.5858/2006-130-437-teoocg.

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13

Hanbali, Fadi, Gregory N. Fuller, Norman E. Leeds und Raymond Sawaya. „Choroid plexus cyst and chordoid glioma“. Neurosurgical Focus 10, Nr. 6 (Juni 2001): 1–6. http://dx.doi.org/10.3171/foc.2001.10.6.6.

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Several types of mass lesions may occur in the third and lateral ventricles. Typically they arise from the lining of the ventricular cavity or from contiguous structures, by extension into the ventricle. The authors describe two patients, each of whom presented with a different rare lesion of the ventricular system. The first was a 53-year-old woman with a history of hypertension who sustained a blunt traumatic injury to the occipital region and subsequently developed a progressively worsening right-sided headache. Radiological examinations over the next 2 years revealed an enlarged right lateral ventricle and, ultimately, a choroid plexus cyst in its anterior and middle third, near the foramen of Monro, which is a rare location for these lesions. The cyst was removed en bloc, and follow-up examinations showed a significant improvement in her headache and a minimal differences in size between right and left ventricles. The authors also describe a 57-year-old man with hypertension, diabetes mellitus, and an old mycardial infarct, who presented to an outside institution with a progressively worsening headache, generalized malaise, and loss of olfactory sensation. Diagnostic imaging revealed a 1.5-cm oval lesion centered in the lamina terminalis region, an open craniotomy was performed, and evaluation of a biopsy sample demonstrated the mass to be a chordoid glioma of the third ventricle, a recently described glioma subtype. Two days after surgery, he suffered a left parietal stroke and an anterior mycardial infarction. After convalescing, he presented to The University of Texas M. D. Anderson Cancer Center for radiotherapy and follow up; 7 months later he was readmitted complaining of headache, short-term memory loss, and worsening confusion and disorientation. Neuroimaging revealed progression of the tumor (now 2 cm in diameter), which was removed by gross-total resection. His headache resolved immediately, and 2 months later his only complaint was of episodes of confusion. Three weeks later he died of a massive myocardial infarction. These two patients represent the sixth case of an adult with a choroid plexus cyst in the anterior lateral ventricle and the 19th case of an adult with a chordoid glioma of the third ventricle, respectively.

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14

Muthusamy, RajeshwariK, und SangitaS Mehta. „Chordoid Glioma of the Third Ventricle“. Neurology India 67, Nr. 4 (2019): 1178. http://dx.doi.org/10.4103/0028-3886.266267.

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15

Moomjian, Lauren, Chun-Der Li, Yinghua Pang, Francisco A. DeLara und Daniel E. Meltzer. „Chordoid Glioma of the Third Ventricle“. Neurographics 2, Nr. 3 (01.09.2012): 103–5. http://dx.doi.org/10.3174/ng.3120034.

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16

Cenacchi, G., F. Roncaroli, S. Cerasoli, G. Ficarra, G. A. Merli und F. Giangaspero. „Chordoid Glioma of the Third Ventricle“. American Journal of Surgical Pathology 25, Nr. 3 (März 2001): 401–5. http://dx.doi.org/10.1097/00000478-200103000-00016.

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17

Pasquier, Basile, Michel Péoc'h, Alan L. Morrison, Emmanuel Gay, Dominique Pasquier, Sylvie Grand, Marc Sindou und Nicolas Kopp. „Chordoid Glioma of the Third Ventricle“. American Journal of Surgical Pathology 26, Nr. 10 (Oktober 2002): 1330–42. http://dx.doi.org/10.1097/00000478-200210000-00010.

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18

Zarghouni, Mehrzad, Clayton Vandergriff, Kennith F. Layton, J. Brad Mcgowan, Caetano Coimbra, Amol Bhakti und Michael J. Opatowsky. „Chordoid Glioma of the Third Ventricle“. Baylor University Medical Center Proceedings 25, Nr. 3 (Juli 2012): 285–86. http://dx.doi.org/10.1080/08998280.2012.11928853.

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19

Al-Zubidi, Nagham, Margaret M. McGlynn, Patricia Chévez-Barrios, Sushma Yalamanchili und Andrew G. Lee. „Neuro-Ophthalmologic Features of Chordoid Glioma“. Journal of Neuro-Ophthalmology 34, Nr. 1 (März 2014): 47–49. http://dx.doi.org/10.1097/wno.0b013e3182a595b7.

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20

Takei, Hidehiro, Meenakshi B. Bhattacharjee und Adekunle M. Adesina. „Chordoid Glioma of the Third Ventricle“. Acta Cytologica 50, Nr. 6 (2006): 691–96. http://dx.doi.org/10.1159/000326044.

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21

Destefani, Marília Henrique, Alessandro Spanó Mello, Ricardo Santos de Oliveira und Gustavo Novelino Simão. „Chordoid glioma of the third ventricle“. Radiologia Brasileira 48, Nr. 5 (Oktober 2015): 338–39. http://dx.doi.org/10.1590/0100-3984.2014.0125.

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22

Baehring, Joachim M., und Serguei Bannykh. „Chordoid Glioma of the Third Ventricle“. Journal of Neuro-Oncology 76, Nr. 3 (Februar 2006): 269. http://dx.doi.org/10.1007/s11060-006-6054-y.

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23

Scheurkogel, Merel M., Sjoerd G. van Duinen, Marco J. T. Verstegen und Geert J. Lycklama à Nijeholt. „Chordoid glioma: a rare suprasellar mass“. Acta Neurologica Belgica 112, Nr. 3 (30.05.2012): 311–14. http://dx.doi.org/10.1007/s13760-012-0084-3.

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24

Vanhauwaert, D. J., F. Clement, J. Van Dorpe und M. J. Deruytter. „Chordoid glioma of the third ventricle“. Acta Neurochirurgica 150, Nr. 11 (21.10.2008): 1183–91. http://dx.doi.org/10.1007/s00701-008-0014-6.

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25

Cunha, Pedro, Olinda Rebelo und Marcos Barbosa. „Chordoid Glioma of the Third Ventricle, a Rare Tumor with an Unexpected Outcome“. Arquivos Brasileiros de Neurocirurgia: Brazilian Neurosurgery 36, Nr. 01 (17.02.2017): 32–37. http://dx.doi.org/10.1055/s-0037-1599062.

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Chordoid glioma is a rare tumor of the third ventricle whose imaging features are difficult to distinguish from other more common lesions in this location. There are only 83 cases described so far in the literature. Although gross total resection (GTR) is the treatment of choice, immediate postoperative mortality with this approach can be as high as 29%, and morbidity among survivors can reach 67%. We report a case of a male patient of advanced age, with a third ventricle mass lesion, who presented with a progressive right temporal hemianopia. Imaging was compatible with craniopharyngioma, meningioma or even metastasis. Chordoid glioma was not considered in the differential diagnosis. The patient underwent surgery and GTR was achieved. There were no postoperative complications, and the patient was discharged from the hospital three weeks later. Unexpectedly, two days afterwards, he suffered a major brainstem hemorrhagic stroke and, unfortunately, died.

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Buccoliero, Anna Maria, Adele Caldarella, Pasquale Gallina, Nicola Di Lorenzo, Antonio Taddei und Gian Luigi Taddei. „Chordoid Glioma: Clinicopathologic Profile and Differential Diagnosis of an Uncommon Tumor“. Archives of Pathology & Laboratory Medicine 128, Nr. 11 (01.11.2004): e141-e145. http://dx.doi.org/10.5858/2004-128-e141-cgcpad.

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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 remained alive and well 8 months after the surgery. Histologically, the tumor consisted of clusters and cords of epithelioid cells embedded in a mucinous matrix. Lymphoplasmacytic infiltrates and Russell bodies were prominent. Immunohistochemically, the tumor cells were positive for glial fibrillary acidic protein, neurofilaments, and neuron-specific enolase, suggesting a divergent neuronal and glial differentiation. The Ki-67 index was low. The clinicopathologic profile and the differential diagnosis of this tumor are discussed.

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Dias, Lídia. „Incidental Third Ventricular Chordoid Glioma: Case Report“. Sinapse 21, Nr. 1 (16.04.2021): 59–61. http://dx.doi.org/10.46531/sinapse/cc/200071/2021.

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28

Gallina, Pasquale, Gastone Pansini, Homere Mouchaty, Regina Mura, AnnaMaria Buccoliero und NicolaDi Lorenzo. „An incidentally detected third ventricle chordoid glioma“. Neurology India 55, Nr. 4 (2007): 406. http://dx.doi.org/10.4103/0028-3886.33301.

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29

Yao, Kun, Zejun Duan, Zunguo Du, Xiaolong Fan, Yanming Qu, Mingshan Zhang, Yin Wang, Hailong Liu, Lingyan Sun und Xueling Qi. „PRKCA D463H Mutation in Chordoid Glioma of the Third Ventricle: A Cohort of 16 Cases, Including Two Cases Harboring BRAFV600E Mutation“. Journal of Neuropathology & Experimental Neurology 79, Nr. 11 (17.10.2020): 1183–92. http://dx.doi.org/10.1093/jnen/nlaa107.

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Abstract Chordoid gliomas (CG) of the third ventricle are characterized by chordoid and glial features, but the extent of histological variations across CG is not fully understood. Herein, we report 16 consecutive cases of CG. All 16 patients had histories of headache and vision loss; their median age was 41.7 years at the surgery. Histological examination revealed typical features of CG, including cords of epithelioid cells within the mucinous stroma and lymphoplasmacytic infiltration. Two cases exhibited atypical histological features including histiocyte-like cells. PRKCA mutation was found in 14 cases, including the 2 with histiocytic features. BRAFV600E mutation was found only in the 2 cases with histiocytic features. The patients underwent gross total tumor resection without radiotherapy or chemotherapy. Three patients died between 1 and 4 months postsurgery. Only one had a recurrence. Eleven were alive at the most recent follow-up (range: 2–58 months). These data indicate that PRKCA mutation was a good diagnostic marker for CG and additionally suggest that histiocyte-like features can be present in CG in association with BRAF mutations.

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JUNG, Tae-Young, und Shin JUNG. „Third Ventricular Chordoid Glioma With Unusual Aggressive Behavior“. Neurologia medico-chirurgica 46, Nr. 12 (2006): 605–8. http://dx.doi.org/10.2176/nmc.46.605.

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31

Suh, Yeon-Lim, Na Rae Kim, Jong-Hyun Kim und Sung-Hye Park. „Suprasellar chordoid glioma combined with Rathke's cleft cyst“. Pathology International 53, Nr. 11 (November 2003): 780–85. http://dx.doi.org/10.1046/j.1440-1827.2003.01549.x.

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32

Castro-Dufourny, Inés, Rodrigo Carrasco und José M. Pascual. „Chordoid glioma: A new paradigm of hypothalamic dysfunction?“ Pituitary 20, Nr. 3 (31.10.2016): 393–94. http://dx.doi.org/10.1007/s11102-016-0771-9.

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33

Danilowicz, Karina, Santiago Gonzalez Abbati, Soledad Sosa, Florencia Lustig Witis und Gustavo Sevlever. „Suprasellar chordoid glioma: a report of two cases“. Archives of Endocrinology and Metabolism 62, Nr. 6 (2018): 648–54. http://dx.doi.org/10.20945/2359-3997000000092.

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34

Brat, Daniel J., Bernd W. Scheithauer, Susan M. Staugaitis, Selina C. Cortez, Keith Brecher und Peter C. Burger. „Third Ventricular Chordoid Glioma: A Distinct Clinicopathologic Entity“. Journal of Neuropathology & Experimental Neurology 57, Nr. 3 (März 1998): 283–90. http://dx.doi.org/10.1097/00005072-199803000-00009.

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35

Can, Bilge. „Cytology of chordoid glioma of the third ventricle“. Diagnostic Cytopathology 40, Nr. 2 (06.01.2011): 185–87. http://dx.doi.org/10.1002/dc.21619.

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36

Boukobza, M., M. Peyre, G. Lot, J. Mikol und J. J. Merland. „NO45 Gliome chordoide du troisieme ventricule. Aspects TDM et IRM. A propos d’un cas“. Journal de Radiologie 85, Nr. 9 (September 2004): 1526. http://dx.doi.org/10.1016/s0221-0363(04)77740-9.

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37

Astafyeva, L. I., I. N. Badmaeva, I. S. Klochkova, Yu G. Sidneva, O. I. Sharipov, O. A. Gadjieva, B. A. Bashiryan, P. L. Kalinin, A. Yu Lubnin und A. N. Konovalov. „Reset osmostat syndrome — when hyponatremia become «a normal»: diagnostics, case report“. Problems of Endocrinology 69, Nr. 5 (11.11.2023): 65–72. http://dx.doi.org/10.14341/probl13235.

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Reset osmostat syndrome (ROS) is characterized by a change of normal plasma osmolality threshold (decrease or increase), which leads to chronic dysnatremia (hypo- or hypernatremia). We have described a clinical case of ROS and chronic hyponatremia in a patient with chordoid glioma of the III ventricle. It is known that the patient had previously been diagnosed with hyponatremia (131–134 mmol/l). She has not hypothyroidism and hypocorticism. There is normal filtration function of the kidneys was (CKD-EPI 91.7 ml/mi/1,73m2). Urine osmolality and sodium level were studied to exclude of concentration kidney function disorder. During first three days after removal of the tumor of the third ventricle (chordoid glioma, WHO Grade II), the sodium level decreased to 119 mmol/l. Repeated infusions of 200–300 ml hypertonic 3% sodium chloride solution, gluco- and mineralocorticoid therapy was ineffective, increasing plasma sodium levels by 2–3 mmol/l with the return to the initial level during 6–8 hours. Hypopituitary disorders did not develop after surgery. With further observation, the sodium level remained within 126–129 mmol/l for 6 months after surgery. The water load test make exclude the classic syndrome of inappropriate secretion of antidiuretic hormone, and confirmed the diagnosis of RSO. Because of absence of clinical symptoms associated with hyponatremia, no medical correction was required, patient was recommended to clinical follow-up.

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KOBAYASHI, Tatsuya, Takahiko TSUGAWA, Chisa HASHIZUME, Norio ARITA, Hisashi HATANO, Kenichiro IWAMI, Yoichi NAKAZATO und Yoshimasa MORI. „Therapeutic Approach to Chordoid Glioma of the Third Ventricle“. Neurologia medico-chirurgica 53, Nr. 4 (2013): 249–55. http://dx.doi.org/10.2176/nmc.53.249.

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39

NAKAMURA, Kayoko, Masafumi KITANO, Masakazu FUJIMOTO, Hiromi SAKASHITA und Yoshiaki YUBA. „A case of chordoid glioma of the third ventricle“. Journal of the Japanese Society of Clinical Cytology 50, Nr. 5 (2011): 283–88. http://dx.doi.org/10.5795/jjscc.50.283.

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40

Hung, Nguyen Duy, Nguyen Thanh Van Anh, Duong Dai Ha und Nguyen Minh Duc. „Magnetic resonance imaging of a third ventricular chordoid glioma“. Radiology Case Reports 16, Nr. 8 (August 2021): 1941–45. http://dx.doi.org/10.1016/j.radcr.2021.04.074.

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41

Galloway, F. Afshar, J. F. Geddes, M. „Chordoid glioma: an uncommon tumour of the third ventricle“. British Journal of Neurosurgery 15, Nr. 2 (Januar 2001): 147–50. http://dx.doi.org/10.1080/02688690120036865.

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42

Vanhauwaert, D., F. Clement, J. Van Dorpe und M. Deruytter. „Chordoid glioma of third ventricle: a rare clinicopathologic entity“. Surgical Neurology 68, Nr. 2 (August 2007): 200. http://dx.doi.org/10.1016/j.surneu.2007.06.052.

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43

Morais, Barbara A., Djalma F. S. Menendez, Raphael S. S. Medeiros, Manoel J. Teixeira und Guilherme A. Lepski. „Chordoid glioma: Case report and review of the literature“. International Journal of Surgery Case Reports 7 (2015): 168–71. http://dx.doi.org/10.1016/j.ijscr.2015.01.027.

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44

Poyuran, Rajalakshmi, Anita Mahadevan, B. K. Chandrasekhar Sagar, Jitender Saini und Dwarakanath Srinivas. „Chordoid Glioma of Third Ventricle With an Epidermoid Cyst“. International Journal of Surgical Pathology 24, Nr. 7 (28.07.2016): 663–67. http://dx.doi.org/10.1177/1066896916650256.

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45

Castellano-Sanchez, Amilcar A., Monica A. Recine, Ricardo Restrepo, Lydia H. Howard und Morton J. Robinson. „Chordoid glioma: A novel tumor of the third ventricle“. Annals of Diagnostic Pathology 4, Nr. 6 (Dezember 2000): 373–78. http://dx.doi.org/10.1053/adpa.2000.19369.

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46

Kurian, K. M., P. F. X. Statham, C. Smith, J. E. Bell und J. W. Ironside. „Third ventricular chordoid glioma: clinicopathological features of two cases“. Neuropathology and Applied Neurobiology 28, Nr. 2 (März 2002): 165. http://dx.doi.org/10.1046/j.1365-2990.2002.39286_46.x.

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47

Carrasco-Moro, Rodrigo, Inés Castro-Dufourny, Ruth Prieto und José M. Pascual. „Transphenoidal Surgery : The Optimal Approach to Chordoid Gliomas of the Third Ventricle?“ Journal of Korean Neurosurgical Society 61, Nr. 6 (01.11.2018): 774–76. http://dx.doi.org/10.3340/jkns.2017.0221.

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48

Goyal, R., R. K. Vashishta, S. Singhi und M. Gill. „Extraventricular unusual glioma in a child with extensive myxoid change resembling chordoid glioma“. Journal of Clinical Pathology 60, Nr. 11 (01.11.2007): 1294–95. http://dx.doi.org/10.1136/jcp.2005.033548.

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49

Lee, Yat Sing, Tsz Wai Yeung und On Cheung Leung. „One of a kind—chordoid glioma in the fourth ventricle: a case report and literature review“. Acta Radiologica Open 9, Nr. 12 (Dezember 2020): 205846012098014. http://dx.doi.org/10.1177/2058460120980143.

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Annotation:

Chordoid glioma (CG) is a rare brain tumor that is known for its characteristic location in the third ventricle. A wide spectrum of radiological presentations has been described, with few common features among them. Its radiological diagnosis is mainly suggested by location. However, several cases of CG with atypical locations have been described, illustrating that CG is not limited to the third ventricle, and should be considered in the list of radiological differential diagnosis for intraventricular masses. We present here a case of CG that was found in the fourth ventricle.

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50

Petrecca, Kevin, und QasimS Al Hinai. „Rarest of the rare: Chordoid glioma infiltrating the optic chiasm“. Surgical Neurology International 2, Nr. 1 (2011): 53. http://dx.doi.org/10.4103/2152-7806.80118.

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