Articles de revues : « Chordoid Glioma »

1

Thavaratnam, LK, ST Loy, A. Gupta, I. Ng et JF Cullen. « Chordoid glioma ». Singapore Medical Journal 56, n^o 11 (novembre 2015) : 641–43. http://dx.doi.org/10.11622/smedj.2015175.

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Liu, Wei-ping, Jin-xiang Cheng, Xi-cai Yi, Hai-ning Zhen, Zhou Fei, Qing Li et Xiang Zhang. « Chordoid Glioma ». Neurologist 17, n^o 1 (janvier 2011) : 52–56. http://dx.doi.org/10.1097/nrl.0b013e3181e7db67.

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Leeds, Norman E., Frederick F. Lang, Teresa Ribalta, Raymond Sawaya et Gregory N. Fuller. « Origin of Chordoid Glioma of the Third Ventricle ». Archives of Pathology & ; Laboratory Medicine 130, n^o 4 (1 avril 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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Ricoy, J. R., R. D. Lobato, B. Báez, A. Cabello, M. A. Martínez et G. Rodríguez. « Suprasellar chordoid glioma ». Acta Neuropathologica 99, n^o 6 (9 juin 2000) : 699–703. http://dx.doi.org/10.1007/s004010051183.

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Brat, D. J., B. W. Scheithauer, S. C. Cortez, K. Brecher et P. C. Burger. « THIRD VENTRICULAR “CHORDOID GLIOMA” ». Journal of Neuropathology and Experimental Neurology 56, n^o 5 (mai 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, n^o 1 (janvier 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 et Gian Luigi Taddei. « Chordoid Glioma : Clinicopathologic Profile and Differential Diagnosis of an Uncommon Tumor ». Archives of Pathology & ; Laboratory Medicine 128, n^o 11 (1 novembre 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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8

Sanda, Nicolae, Claudiu-Nicolae Mircea, Michèle Bernier, Avinoam B. Safran et Sorin Aldea. « Chordoid Glioma Infiltrating Optic Structures ». Journal of Neuro-Ophthalmology 39, n^o 3 (septembre 2019) : 408–10. http://dx.doi.org/10.1097/wno.0000000000000757.

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Castellano-Sanchez, Amilcar Antonio, Erwin Schemankewitz, Claire Mazewski et Daniel J. Brat. « Pediatric Chordoid Glioma withChondroid Metaplasia ». Pediatric and Developmental Pathology 4, n^o 6 (1 novembre 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, n^o 4 (1 avril 2006) : 437–38. http://dx.doi.org/10.5858/2006-130-437-teoocg.

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Hanbali, Fadi, Gregory N. Fuller, Norman E. Leeds et Raymond Sawaya. « Choroid plexus cyst and chordoid glioma ». Neurosurgical Focus 10, n^o 6 (juin 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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12

Muthusamy, RajeshwariK, et SangitaS Mehta. « Chordoid Glioma of the Third Ventricle ». Neurology India 67, n^o 4 (2019) : 1178. http://dx.doi.org/10.4103/0028-3886.266267.

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Moomjian, Lauren, Chun-Der Li, Yinghua Pang, Francisco A. DeLara et Daniel E. Meltzer. « Chordoid Glioma of the Third Ventricle ». Neurographics 2, n^o 3 (1 septembre 2012) : 103–5. http://dx.doi.org/10.3174/ng.3120034.

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Cenacchi, G., F. Roncaroli, S. Cerasoli, G. Ficarra, G. A. Merli et F. Giangaspero. « Chordoid Glioma of the Third Ventricle ». American Journal of Surgical Pathology 25, n^o 3 (mars 2001) : 401–5. http://dx.doi.org/10.1097/00000478-200103000-00016.

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15

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

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Zarghouni, Mehrzad, Clayton Vandergriff, Kennith F. Layton, J. Brad Mcgowan, Caetano Coimbra, Amol Bhakti et Michael J. Opatowsky. « Chordoid Glioma of the Third Ventricle ». Baylor University Medical Center Proceedings 25, n^o 3 (juillet 2012) : 285–86. http://dx.doi.org/10.1080/08998280.2012.11928853.

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17

Al-Zubidi, Nagham, Margaret M. McGlynn, Patricia Chévez-Barrios, Sushma Yalamanchili et Andrew G. Lee. « Neuro-Ophthalmologic Features of Chordoid Glioma ». Journal of Neuro-Ophthalmology 34, n^o 1 (mars 2014) : 47–49. http://dx.doi.org/10.1097/wno.0b013e3182a595b7.

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18

Takei, Hidehiro, Meenakshi B. Bhattacharjee et Adekunle M. Adesina. « Chordoid Glioma of the Third Ventricle ». Acta Cytologica 50, n^o 6 (2006) : 691–96. http://dx.doi.org/10.1159/000326044.

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19

Destefani, Marília Henrique, Alessandro Spanó Mello, Ricardo Santos de Oliveira et Gustavo Novelino Simão. « Chordoid glioma of the third ventricle ». Radiologia Brasileira 48, n^o 5 (octobre 2015) : 338–39. http://dx.doi.org/10.1590/0100-3984.2014.0125.

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20

Baehring, Joachim M., et Serguei Bannykh. « Chordoid Glioma of the Third Ventricle ». Journal of Neuro-Oncology 76, n^o 3 (février 2006) : 269. http://dx.doi.org/10.1007/s11060-006-6054-y.

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Scheurkogel, Merel M., Sjoerd G. van Duinen, Marco J. T. Verstegen et Geert J. Lycklama à Nijeholt. « Chordoid glioma : a rare suprasellar mass ». Acta Neurologica Belgica 112, n^o 3 (30 mai 2012) : 311–14. http://dx.doi.org/10.1007/s13760-012-0084-3.

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22

Vanhauwaert, D. J., F. Clement, J. Van Dorpe et M. J. Deruytter. « Chordoid glioma of the third ventricle ». Acta Neurochirurgica 150, n^o 11 (21 octobre 2008) : 1183–91. http://dx.doi.org/10.1007/s00701-008-0014-6.

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23

Suetens, Kristin, Jeroen Swinnen, Linde Stessens, Sofie Van Cauter et 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 (4 décembre 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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24

Dias, Lídia. « Incidental Third Ventricular Chordoid Glioma : Case Report ». Sinapse 21, n^o 1 (16 avril 2021) : 59–61. http://dx.doi.org/10.46531/sinapse/cc/200071/2021.

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Gallina, Pasquale, Gastone Pansini, Homere Mouchaty, Regina Mura, AnnaMaria Buccoliero et NicolaDi Lorenzo. « An incidentally detected third ventricle chordoid glioma ». Neurology India 55, n^o 4 (2007) : 406. http://dx.doi.org/10.4103/0028-3886.33301.

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Cunha, Pedro, Olinda Rebelo et Marcos Barbosa. « Chordoid Glioma of the Third Ventricle, a Rare Tumor with an Unexpected Outcome ». Arquivos Brasileiros de Neurocirurgia : Brazilian Neurosurgery 36, n^o 01 (17 février 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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27

JUNG, Tae-Young, et Shin JUNG. « Third Ventricular Chordoid Glioma With Unusual Aggressive Behavior ». Neurologia medico-chirurgica 46, n^o 12 (2006) : 605–8. http://dx.doi.org/10.2176/nmc.46.605.

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Suh, Yeon-Lim, Na Rae Kim, Jong-Hyun Kim et Sung-Hye Park. « Suprasellar chordoid glioma combined with Rathke's cleft cyst ». Pathology International 53, n^o 11 (novembre 2003) : 780–85. http://dx.doi.org/10.1046/j.1440-1827.2003.01549.x.

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Castro-Dufourny, Inés, Rodrigo Carrasco et José M. Pascual. « Chordoid glioma : A new paradigm of hypothalamic dysfunction ? » Pituitary 20, n^o 3 (31 octobre 2016) : 393–94. http://dx.doi.org/10.1007/s11102-016-0771-9.

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

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31

Brat, Daniel J., Bernd W. Scheithauer, Susan M. Staugaitis, Selina C. Cortez, Keith Brecher et Peter C. Burger. « Third Ventricular Chordoid Glioma : A Distinct Clinicopathologic Entity ». Journal of Neuropathology & ; Experimental Neurology 57, n^o 3 (mars 1998) : 283–90. http://dx.doi.org/10.1097/00005072-199803000-00009.

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32

Can, Bilge. « Cytology of chordoid glioma of the third ventricle ». Diagnostic Cytopathology 40, n^o 2 (6 janvier 2011) : 185–87. http://dx.doi.org/10.1002/dc.21619.

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33

Goyal, R., R. K. Vashishta, S. Singhi et M. Gill. « Extraventricular unusual glioma in a child with extensive myxoid change resembling chordoid glioma ». Journal of Clinical Pathology 60, n^o 11 (1 novembre 2007) : 1294–95. http://dx.doi.org/10.1136/jcp.2005.033548.

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34

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

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

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36

Hung, Nguyen Duy, Nguyen Thanh Van Anh, Duong Dai Ha et Nguyen Minh Duc. « Magnetic resonance imaging of a third ventricular chordoid glioma ». Radiology Case Reports 16, n^o 8 (août 2021) : 1941–45. http://dx.doi.org/10.1016/j.radcr.2021.04.074.

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37

Galloway, F. Afshar, J. F. Geddes, M. « Chordoid glioma : an uncommon tumour of the third ventricle ». British Journal of Neurosurgery 15, n^o 2 (janvier 2001) : 147–50. http://dx.doi.org/10.1080/02688690120036865.

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38

Vanhauwaert, D., F. Clement, J. Van Dorpe et M. Deruytter. « Chordoid glioma of third ventricle : a rare clinicopathologic entity ». Surgical Neurology 68, n^o 2 (août 2007) : 200. http://dx.doi.org/10.1016/j.surneu.2007.06.052.

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39

Morais, Barbara A., Djalma F. S. Menendez, Raphael S. S. Medeiros, Manoel J. Teixeira et 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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40

Poyuran, Rajalakshmi, Anita Mahadevan, B. K. Chandrasekhar Sagar, Jitender Saini et Dwarakanath Srinivas. « Chordoid Glioma of Third Ventricle With an Epidermoid Cyst ». International Journal of Surgical Pathology 24, n^o 7 (28 juillet 2016) : 663–67. http://dx.doi.org/10.1177/1066896916650256.

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41

Castellano-Sanchez, Amilcar A., Monica A. Recine, Ricardo Restrepo, Lydia H. Howard et Morton J. Robinson. « Chordoid glioma : A novel tumor of the third ventricle ». Annals of Diagnostic Pathology 4, n^o 6 (décembre 2000) : 373–78. http://dx.doi.org/10.1053/adpa.2000.19369.

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42

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

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Petrecca, Kevin, et QasimS Al Hinai. « Rarest of the rare : Chordoid glioma infiltrating the optic chiasm ». Surgical Neurology International 2, n^o 1 (2011) : 53. http://dx.doi.org/10.4103/2152-7806.80118.

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NAKANO, Mariko, Yoshifumi ASAKURA, Manabu YAMASHITA, Toshie TERAUCHI, Nozomu KUROSE, Takayuki NOJIMA et Hideaki IIZUKA. « A case report of chordoid glioma of the third ventricle. » Journal of the Japanese Society of Clinical Cytology 39, n^o 3 (2000) : 208–12. http://dx.doi.org/10.5795/jjscc.39.208.

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Tonami, Hisao, Maya Kamehiro, Manabu Oguchi, Kotaro Higashi, Itaru Yamamoto, Takayuki Nojima, Kazuya Okamoto, Takuya Akai et Hideaki Iizuka. « Chordoid Glioma of the Third Ventricle : CT and MR Findings ». Journal of Computer Assisted Tomography 24, n^o 2 (mars 2000) : 336–38. http://dx.doi.org/10.1097/00004728-200003000-00029.

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Mittal, R., Amitesh Dubey, S. Singhvi et Manash Bora. « Atypical Chordoid Glioma of the Third Ventricle : A Case Report ». Indian Journal of Neurosurgery 04, n^o 02 (28 juillet 2015) : 124–27. http://dx.doi.org/10.1055/s-0035-1558838.

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Michotte, A., J. Van Der Veken, M. Huylebrouck, J. Duerinck, J. D'Haens et A. Hoorens. « Expression of thyroid transcription factor 1 in a chordoid glioma ». Journal of the Neurological Sciences 346, n^o 1-2 (novembre 2014) : 362–63. http://dx.doi.org/10.1016/j.jns.2014.09.005.

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48

Tu, A., T. Yeo, D. Steinke, L. Resch et V. Mehta. « Chordoid Glioma : Imaging Pearls of a Unique Third Ventricular Tumor ». Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 37, n^o 5 (septembre 2010) : 677–80. http://dx.doi.org/10.1017/s031716710001088x.

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Romero-Rojas, Alfredo E., Julio A. Díaz-Pérez et Lina M. Ariza-Serrano. « CD99 is expressed in chordoid glioma and suggests ependymal origin ». Virchows Archiv 460, n^o 1 (20 novembre 2011) : 119–22. http://dx.doi.org/10.1007/s00428-011-1170-2.

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Jain, D., M. C. Sharma, C. Sarkar, V. Suri, A. Rishi, A. Garg et S. Vaishya. « Chordoid glioma : report of two rare examples with unusual features ». Acta Neurochirurgica 150, n^o 3 (4 février 2008) : 295–300. http://dx.doi.org/10.1007/s00701-008-1420-x.

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