WordNet
- tumor of the pineal gland
Wikipedia preview
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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Pinealoblastoma |
Classification and external resources |
ICD-10 |
C75.3 |
ICD-O: |
9362/3 |
MeSH |
D010871 |
Pinealoblastoma is a tumor of the pineal gland.
Retinoblastoma can be characterized as "bilateral" when it presents on both sides. It can also be characterized as "trilateral" when it presents with pinealoblastoma.[1]
References [edit]
- ^ Provenzale JM, Weber AL, Klintworth GK, McLendon RE (January 1995). "Radiologic-pathologic correlation. Bilateral retinoblastoma with coexistent pinealoblastoma (trilateral retinoblastoma)". AJNR Am J Neuroradiol 16 (1): 157–65. PMID 7900586.
See also [edit]
- Primitive neuroectodermal tumor
Tumors: endocrine gland neoplasia (C73–C75/D34–D35, 193–194/226–227)
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Pancreas/
islets of Langerhans |
- neuroendocrine tumors/islet cell carcinoma: α: Glucagonoma
- β: Insulinoma
- δ: Somatostatinoma
- G: Gastrinoma
- VIPoma
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Hypothalamic/
pituitary axes
+parathyroid |
Pituitary |
- Pituitary adenoma: Prolactinoma
- ACTH-secreting pituitary adenoma
- GH-secreting pituitary adenoma
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Thyroid |
- Thyroid cancer (malignant): epithelial cell carcinoma
- Papillary
- Follicular/Hurthle cell
- parafollicular cell
- Anaplastic
- Lymphoma
- Squamous cell carcinoma
- Benign: Thyroid adenoma
- Struma ovarii
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Parathyroid |
- Parathyroid adenoma
- Parathyroid carcinoma
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Adrenal tumor |
- adrenal cortex
- Adrenocortical adenoma
- Adrenocortical carcinoma
- adrenal medulla
- Pheochromocytoma
- Neuroblastoma
- see also: Paraganglioma
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Gonads |
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Pinealoma |
- Pinealoblastoma
- Pineocytoma
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MEN |
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noco (d)/cong/tumr, sysi/epon
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proc, drug (A10/H1/H2/H3/H5)
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UpToDate Contents
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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?
- Expression of O6-methylguanine DNA methyltransferase (MGMT) and immunohistochemical analysis of 12 pineal parenchymal tumors
- 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
Related Links
- This website has been created for the sole purpose of CHILDHOOD Pineoblastoma, a PNET maligant brain tumor that arises in the pineal region. ... This website has been created for the sole purpose of CHILDHOOD Pineoblastoma ...
- This website has been created for the sole purpose of CHILDHOOD Pineoblastoma, a PNET maligant brain tumor that arises in the pineal region. ... What Types of Symptoms Are Typical? Because the pineal gland sits just above ...
Related Pictures
★リンクテーブル★
[★]
松果体腫
- 関
- pineal neoplasm、pineal tumor、pineoblastoma、pineocytoma
[★]
松果体腫瘍、松果体部腫瘍
- 関
- pineal neoplasm、pinealoma、pineoblastoma、pineocytoma
[★]
松果体腫瘍、松果体新生物
- 関
- pineal tumor、pinealoma、pineoblastoma、pineocytoma
[★]
- 英
- pineoblastoma
- 関
- 松果体腫瘍、松果体芽細胞腫、松果体腫、松果体細胞腫
[★]
- 英
- pineoblastoma
- 関
- 松果体芽腫
-松果体芽腫