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tumor of the pineal gland

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/05/14 22:58:49」(JST)

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1. 松果体部腫瘍 pineal gland masses
2. まれな脳腫瘍 uncommon brain tumors
3. 固形腫瘍による軟髄膜転移の臨床的特徴および診断 clinical features and diagnosis of leptomeningeal metastases from solid tumors
4. 網膜芽細胞腫の概要 overview of retinoblastoma

English Journal

Clinical and neurophysiological changes in patients with pineal region expansions.

Hajnsek S, Paladino J, Gadze ZP, Nanković S, Mrak G, Lupret V.SourceUniversity of Zagreb, Zagreb University Hospital Centre, School of Medicine, Department of Neurology, Zagreb, Croatia.
Collegium antropologicum.Coll Antropol.2013 Mar;37(1):35-40.
In the last 20 years neurological and neurosurgical follow up of our patients with pineal region expansions (118 patients) pointed to certain clinical and neurophysiological regularities. We performed retrospective study which included 84 patients with pineal region expansions in the period from 199
PMID 23697248

Clinicopathologic Study of Pineal Parenchymal Tumors of Intermediate Differentiation (PPTID).

Ito T, Kanno H, Sato KI, Oikawa M, Ozaki Y, Nakamura H, Terasaka S, Kobayashi H, Houkin K, Hatanaka K, Murata JI, Tanaka S.SourceDepartment of Neurosurgery, Brain Tumor Center, Nakamura Memorial Hospital, Sapporo, Japan. Electronic address: titoh@med.nmh.or.jp.
World neurosurgery.World Neurosurg.2013 Feb 8. pii: S1878-8750(13)00272-6. doi: 10.1016/j.wneu.2013.02.007. [Epub ahead of print]
OBJECTIVE: Pineal parenchymal tumors of intermediate differentiation (PPTID) are extremely rare tumor entities, and only limited data are available regarding their pathologic features and biologic behaviors. Because grading criteria of pineal parenchymal tumors (PPTs) have yet to be established, the
PMID 23396072

Treatment of young children with CNS-primitive neuroectodermal tumors/pineoblastomas in the prospective multicenter trial HIT 2000 using different chemotherapy regimens and radiotherapy.

Friedrich C, von Bueren AO, von Hoff K, Gerber NU, Ottensmeier H, Deinlein F, Benesch M, Kwiecien R, Pietsch T, Warmuth-Metz M, Faldum A, Kuehl J, Kortmann RD, Rutkowski S.SourceDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Martinistr. 52, D-20246 Hamburg, Germany.
Neuro-oncology.Neuro Oncol.2013 Feb;15(2):224-34. doi: 10.1093/neuonc/nos292. Epub 2012 Dec 7.
BACKGROUND: Especially in young children, primitive neuroectodermal tumors of the central nervous system (CNS-PNET) and pineoblastomas are associated with an unfavorable outcome, and only a few prospective trials have been conducted thus far.METHODS: From January 2001 through January 2005, 17 eligib
PMID 23223339

Japanese Journal

Quantitative imaging values of CT, MR, and FDG-PET to differentiate pineal parenchymal tumors and germinomas: are they useful?

Neuroradiology 56(4), 297-303, 2014-02-09
NAID 120005669342

Expression of O6-methylguanine DNA methyltransferase (MGMT) and immunohistochemical analysis of 12 pineal parenchymal tumors

Neuropathology 32(6), 647-653, 2012-12
NAID 120005356854

Pineal parenchymal tumor of intermediate differentiation showing malignant progression at relapse

Neuropathology : official journal the Japanese Society of Neuropathology 29(5), 602-608, 2009-10-01
NAID 10028192420

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