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Craniopharyngioma Mimicking Chordoid Glioma Shohei Kobayashi 1,2 , Fumiyuki Yamasaki 1 , Masato Kojima 3,4 , Takeshi Takayasu 1 , Motoki Takano 1 , Ushio Yonezawa 1 , Akira Taguchi 1 , Eiso Hiyama 3 , Yasuyuki Kinoshita 1 1Department of Neurosurgery, Hiroshima University Hospital 2Department of Neurosurgery, Hiroshima City Asa Citizens Hospital 3Department of Pediatric Surgery, Hiroshima University Hospital 4Natural Science Center for Basic Research and Development Keyword: 頭蓋咽頭腫 , 第三脳室限局型 , 脊索腫様膠腫 , BRAFV600E変異 , craniopharyngioma , strictly third ventricle , chordoid glioma , BRAFV600E mutation pp.189-194
Published Date 2022/2/1
DOI https://doi.org/10.11477/mf.1416202007
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Abstract

Entirely intrinsic third ventricular craniopharyngiomas showed characteristics of a round/oval shaped tumor, with rare calcification and cyst formation, and pathologically squamous-papillary type with a positive BRAFV600E mutation. We report an extremely rare case of entirely intrinsic third ventricular craniopharyngioma, pathologically adamantiomatous but with BRAFV600E mutation genetically, developed in a 35-year-old female. It was oval-shaped, with no calcification or cyst, and showed homogeneous enhancement. As shown in this case, it was difficult to differentiate this pathology from chordoid glioma of third ventricle, and the difficulty of this differential diagnosis has not been well documented in previous studies. Our case further implied the importance of molecular diagnosis for subclassification of craniopharyngioma. The BRAFV600E-mutated craniopharyngioma could be the target for the development of treatment with preoperative BRAF-inhibitors. Therefore, differentiation between entirely intrinsic third ventricular craniopharyngiomas and chordoid glioma could be new issue. In this report, we discuss about the preoperative differential diagnosis from chordoid glioma and the literature review.

(Received 12 August, 2021; Accepted 21 September, 2021; Published 1 February, 2022)


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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