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1. 視神経膠腫 optic pathway glioma
2. 低悪性度神経膠腫のマネージメント management of low grade glioma
3. 神経線維腫症I型（NF1）：病因、臨床的特徴、および診断 neurofibromatosis type 1 nf1 pathogenesis clinical features and diagnosis
4. 松果体部腫瘍 pineal gland masses
5. 頭蓋照射の遅延合併症 delayed complications of cranial irradiation

García Carretero R1, Romero Brugera M2, Vazquez-Gomez O3, Rebollo-Aparicio N2.
BMJ case reports.BMJ Case Rep.2016 Nov 17;2016. pii: bcr2016218205. doi: 10.1136/bcr-2016-218205.
Chordoid gliomas are rare tumours. Despite being considered low-grade neoplasms, recent reviews have reported generally poor prognosis due to complications involving severe hypothalamic symptoms. We report a patient aged 30 years with chordoid glioma. What makes this case report interesting is the
PMID 27856533

Spontaneous intratumoural and intraventricular haemorrhage associated with a pilomyxoid astrocytoma in the hypothalamic/chiasmatic region.

Wang Z1, Yan HM2, Zhou XR1, Liu JK1, Chang JY1, Wang YT1.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia.J Clin Neurosci.2016 Nov;33:217-220. doi: 10.1016/j.jocn.2016.03.033. Epub 2016 Jul 19.
Pilomyxoid astrocytoma (PMA) is a rare, low-grade glioma that is recognised as a variant of pilocytic astrocytoma. There have been few reports on this pathologic entity presenting with spontaneous haemorrhage. In this study, we report a rare case of PMA in the hypothalamic/chiasmatic region presenti
PMID 27450285

Expanded Endoscopic Transnasal Approach to the Chordoid Glioma of the Third Ventricle : The First Case Ever Reported.

Zeinalizadeh M1, Sadrehosseini SM2, Tayebi Meybodi K3, Sharifabadi AH4.
Journal of Korean Neurosurgical Society.J Korean Neurosurg Soc.2016 Nov;59(6):643-646. Epub 2016 Oct 24.
Chordoid glioma of the third ventricle is a rare and challenging tumor to surgery because of its unique anatomical location and its close juxtaposition to the neurovascular structures and hypothalamus. The authors report a case of chordoid glioma of the third ventricle in a 43-year-old woman, who pr
PMID 27847580

園田順彦,隈部俊宏,齋藤竜太,金森政之,山下洋二,冨永悌二
脳神経外科ジャーナル 21(3), 224-235, 2012-03-20
小児神経膠腫のうち,視経路・視床下部星細胞腫,上衣系腫瘍,脳幹部びまん性神経膠腫の代表的疾患3つを紹介する.視経路・視床下部星細胞腫:まれな疾患であり,組織学的には毛様細胞性星細胞腫が多く,発生にはBRAF遺伝子の異常が関与していることが多い.治療法として,現在は白金製剤を基本とした化学療法が標準治療となっている.上衣系腫瘍:現在,遺伝子変異の解析が網羅的に行われつつある.全摘出術が最良の治療法で …
NAID 110009419599

寺西英人,川崎浩三,齋藤亜紀
小児がん : 小児悪性腫瘍研究会記録 48(3), 334-337, 2011-10-25
低悪性度星細胞腫(LGA)の12歳男児が,再発後も8年以上生存しているので報告する.生後10か月時に視床下部原発LGA髄膜播種と診断され,多剤併用大量化学療法後に末梢血幹細胞移植を施行された.4歳時に残存腫瘍の増大を認め,ビンクリスチン週1回投与で46か月間進行を止めたが,再増大しテモゾロミドでは無効だった.ビンブラスチンを37か月間使用後腫瘍内出血をきたし中断したが腫瘍は増大を止めている.
NAID 110009857591