Chordoid glioma: a clinicopathological study
10.3760/cma.j.cn112151-20210111-00025
- VernacularTitle:脊索样胶质瘤临床病理学观察
- Author:
Leiming WANG
1
;
Liwei SHAO
;
Bo CHENG
;
Huanying ZHAO
;
Lihong ZHAO
;
Yingying YAO
;
Qiuping GUI
;
Dehong LU
;
Lianghong TENG
Author Information
1. 首都医科大学宣武医院病理科，北京 100053
- Keywords:
Glioma;
DNA mutational analysis;
Third ventricle
- From:
Chinese Journal of Pathology
2021;50(8):865-869
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To analyze the clinicopathological features of chordoid glioma.Methods:A total of 12 cases of chordoid gliomas from 2009 to 2020 in Xuanwu Hospital of Capital Medical University and General Hospital of Chinese People′s Liberation Army were retrospectively analyzed. The clinical and imaging characteristics, pathologic and molecular characteristics were analyzed, and the relevant literature was reviewed.Results:All 12 patients (4 males and 8 females) aged from 25 to 67 years (mean 39 years) and mainly had a history of headache or/and vision loss. MRI showed that the lesions located in the third ventricle, and they showed abnormal enhancement. Pathologically, these 12 cases displayed the morphologic characteristics of chordoid gliomas, including papillary structures in two cases. Immunohistochemically, GFAP and vimentin were expressed in all 12 cases (12/12). TTF1 was also expressed in all cases (10/10). CD34 and CKpan were seen in 11 cases (11/12). EMA with dot-and/or-ring like positivity was seen in 9 cases (9/10). Tissues were available in nine chordoid gliomas for Sanger sequencing to detect PRKCA and IDH gene mutation, and eight cases (8/9) showed PRKCA gene D463H mutation. None of these cases showed IDH1 R132 and IDH2 R172 mutation. All 12 patients underwent surgery, and four were lost to follow up. The remaining eight patients were progression or recurrence free at last follow-up in January 2021.Conclusions:Chordoid gliomas have relatively distinguishing clinical and histopathological features. PRKCA gene mutation in chordoid gliomas can be considered as a biomarker for the diagnosis and differential diagnosis of chordoid gliomas, and may provide a direction for future targeted therapy.
