1.Third Ventricular Chordoid Glioma: Case Report.
Sung Nam HWANG ; Seung Won PARK ; Young Baeg KIM ; Duck Young CHOI ; Mi Kyung KIM ; Shin Kwang KHANG
Journal of Korean Neurosurgical Society 2000;29(8):1103-1106
No abstract available.
Glioma*
2.A Case of Nasal Glioma.
Kyun Tae KIM ; Beom Joo LEE ; Sung Ku AHN ; Seung Hun LEE ; Won Soo LEE ; Soo Im CHOI
Annals of Dermatology 1994;6(2):215-218
No abstract available.
Glioma*
3.KSPNO Protocol for Glioma.
Byung Kyu CHO ; Hye Lim JUNG ; Thad T GHIM ; Il Han KIM ; Yong Kil HONG ; Young Shin RA ; Mee Jeong LEE
Korean Journal of Pediatric Hematology-Oncology 2005;12(2):244-285
No abstract available.
Glioma*
4.A Case of Bilateral Thalamic Glioma Presenting with Personality Change.
Kyung Bok LEE ; Jae Ha KIM ; Ji Yoon PARK ; Hakjae ROH ; Moo Young AHN
Journal of the Korean Neurological Association 2007;25(2):278-280
No abstract available.
Glioma*
5.Suprasellar Chordoid Glioma Combined with Rathke's Cleft Cyst: Case Report.
Hyun Wook LEE ; Sang Bok LEE ; Jong Hyun KIM ; Yeon Lim SUH
Journal of Korean Neurosurgical Society 2002;32(4):376-379
Chordoid glioma, a recently introduced clinicopathologic entity, is a rare neoplasm occurring mainly in the third ventricle and hypothalamus. The authors had experienced a case of chordoid glioma combined with Rathke's cleft cyst which occurred in the sellar and suparasellar region. Here we report clinical, radiological, and histopathological features of this neoplasm with review of literature
Glioma*
;
Hypothalamus
;
Third Ventricle
6.The Interaction between GFAP and Fascin in U343 Glioma Cell Line.
Dong Seok KIM ; Seung Woo PARK ; Tae Gon KIM ; Kyu Seung LEE ; Joong Uhn CHOI
Journal of Korean Neurosurgical Society 2004;35(5):507-513
No abstract available.
Cell Line*
;
Glioma*
7.The Feasibility of Histopathological Diagnosis on the Basis of CT Findings in 60 Consecutive Supratentorial Gliomas.
Journal of Korean Neurosurgical Society 1980;9(1):25-38
For assessment of the feasibility of histopathological diagnosis on the basis of CT findings in suratentorial gliomas, 60 consecutive histologically proven cases were analysed. Benign astrocytomas(Kernohan's grade I, I-II, II) were 25, Oligodendrogliomas 6, malignant gliomas(Kernohan's grade III, III-IV, GM) 29 in number. Plain CT findings and degree of peritumoral edema were less significant than the patterns of contrast enhancement in predicting the histological malignancy. Calcification, if present, excluded the diagnosis of malignant gliomas. Combining the CT criteria of pattern of contrast enhancement, degree of peritumoral edema with angiographic signs of malignancy in addition to the clinical feature, a more confident histological diagnosis seemed allowable.
Diagnosis*
;
Edema
;
Glioma*
;
Oligodendroglioma
9.Solitary Primary Leptomeningeal Glioma: Case Report.
Young Goo KIM ; Eui Hyun KIM ; Se Hoon KIM ; Jong Hee CHANG
Brain Tumor Research and Treatment 2013;1(1):36-41
We report a case of solitary primary leptomeningeal glioma. The mass was totally removed under awake surgery. Intraoperatively, no parenchymal involvement was noted. Histopathological study revealed a predominant anaplastic oligodendroglioma component and a focal anaplastic astrocytoma component, which was consistent with an anaplastic oligoastrocytoma. Adjuvant tomotherapy was followed and the tumor has not recurred until 12 months after surgery. A focal type of primary leptomeningeal glioma is extremely rare. We report a rare case of solitary primary leptomeningeal anaplastic oligoastrocytoma.
Astrocytoma
;
Glioma*
;
Oligodendroglioma
10.Metabolic Ratio of FDG-PET and Histologic Grading in Cerebral Gliomas.
Hyung Jin SHIN ; Jong Hyun KIM ; Jung Il LEE ; Ki Joon KIM ; Tae Goo CHO ; Dong Ik SHIN ; Jong Soo KIM ; Seung Chyul HONG ; Kwan PARK ; Whan EOH ; Sun Jung KIM ; Sang Eun KIM ; Yeon Lim SUH
Journal of Korean Neurosurgical Society 1997;26(4):486-490
To assess the degree of malignancy in cerebral gliomas at the time of diagnosis, we compared the metabolic ratio using 18F-fluorodeoxyglucose(FDG)-Positron Emission Tomography(PET) with histologic grading and proliferative index(Ki-67) of cerebral gliomas. Materials for this study were histologically-examined 21 gliomas and they were divided into glioblastomas as group 1, anaplastic gliomas as group 2, and low-grade gliomas as group 3. The visual analysis of FDG-PET images showed hypermetabolic lesions in 14(87.5%) out of 16 high-grade gliomas (glioblastomas and anaplastic gliomas), and hypometabolic lesions in 4(80%) out of 5 low-grade gliomas. Tumor to cerebellum ratio(T/Cbll) in FDG-PET was used as metabolic ratio and the values of T/Cbll in each group were 1.30+/-0.10, 0.73+/-0.07, 0.70+/-0.07, respectively. In comparision of T/Cbll between group 1 with remaining two groups, differences were statistically significant(p=0.0002, p=0.0002, respectively), however, there was no statistical difference between group 2 and group 3. The values of Ki-67 were 24.16+/-5.66 in group 1, 8.10+/-2.70 in group 2, 5.46+/-1.23 in group 3, and differences were statistically significant between group 1 and group 2, 3(p=0.015, p=0.015, respectively), but there was no statistical difference between group 2 and group 3. The correlation between T/Cbll and Ki-67 was good and statistically significant(p=0.0047). In conclusion, the visual and semiquantitative analysis of FDG-PET would be helpful in determining the degree of malignancy in cerebral gliomas.
Cerebellum
;
Diagnosis
;
Glioblastoma
;
Glioma*