神経外胚葉性腫瘍
WordNet
- an abnormal new mass of tissue that serves no purpose (同)tumour, neoplasm
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/11/04 18:27:12」(JST)
[Wiki en表示]
Neuroectodermal tumor |
Classification and external resources |
MeSH |
D018358 |
A neuroectodermal tumor is a tumor of the central or peripheral nervous system.
See also[edit]
- Neuroendocrine tumors
- Neuroectoderm
- PNET
- Medulloblastoma
External links[edit]
- Neuroectodermal tumor entry in the public domain NCI Dictionary of Cancer Terms
This article incorporates public domain material from the U.S. National Cancer Institute document "Dictionary of Cancer Terms".
Nervous tissue tumors/NS neoplasm/Neuroectodermal tumor (ICD-O 9350–9589) (C70–C72, D32–D33, 191–192/225)
|
|
Endocrine/
sellar (9350–9379) |
sellar: Craniopharyngioma · Pituicytoma
other: Pinealoma
|
|
CNS
(9380–9539) |
Neuroepithelial
(brain tumors,
spinal tumors)
|
Glioma
|
Astrocyte
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Astrocytoma (Pilocytic astrocytoma, Pleomorphic xanthoastrocytoma, Fibrillary (also diffuse or lowgrade) astrocytomas, Anaplastic astrocytoma, Glioblastoma multiforme)
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Oligodendrocyte
|
Oligodendroglioma
|
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Ependyma
|
Ependymoma · Subependymoma
|
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Choroid plexus
|
Choroid plexus tumor (Choroid plexus papilloma, Choroid plexus carcinoma)
|
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Multiple/unknown
|
Oligoastrocytoma · Gliomatosis cerebri · Gliosarcoma
|
|
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Mature
neuron
|
Ganglioneuroma: Ganglioglioma · Retinoblastoma · Neurocytoma · Dysembryoplastic neuroepithelial tumour · Lhermitte-Duclos disease
|
|
PNET
|
Neuroblastoma (Esthesioneuroblastoma, Ganglioneuroblastoma) · Medulloblastoma · Atypical teratoid rhabdoid tumor
|
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Primitive
|
Medulloepithelioma
|
|
|
Meningiomas
(meninges)
|
Meningioma, Hemangiopericytoma
|
|
Hematopoietic
|
Primary central nervous system lymphoma
|
|
|
PNS: NST
(9540–9579) |
cranial and paraspinal nerves: Neurofibroma (Neurofibrosarcoma, Neurofibromatosis) · Neurilemmoma/Schwannoma (Acoustic neuroma) · Malignant peripheral nerve sheath tumor
|
|
note: not all brain tumors are of nervous tissue, and not all nervous tissue tumors are in the brain (see brain metastases)
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anat (n/s/m/p/4/e/b/d/c/a/f/l/g)/phys/devp
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noco (m/d/e/h/v/s)/cong/tumr, sysi/epon, injr
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proc, drug (N1A/2AB/C/3/4/7A/B/C/D)
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anat (h/r/t/c/b/l/s/a)/phys (r)/devp/prot/nttr/nttm/ntrp
|
noco/auto/cong/tumr, sysi/epon, injr
|
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UpToDate Contents
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English Journal
- Severe adverse events from the treatment of advanced melanoma: a systematic review of severe side effects associated with ipilimumab, vemurafenib, interferon alfa-2b, dacarbazine and interleukin-2.
- Ma C1, Armstrong AW.
- The Journal of dermatological treatment.J Dermatolog Treat.2014 Oct;25(5):401-8. doi: 10.3109/09546634.2013.813897. Epub 2013 Jul 3.
- BACKGROUND: Current immunomodulatory agents for stage III and IV melanoma exert different mechanisms of action that manifest in distinct adverse events.OBJECTIVE: This systematic review aims to synthesize safety data from clinical trials on ipilimumab, vemurafenib, interferon (IFN) alfa-2b, dacarbaz
- PMID 23763243
- Multidisciplinary management in Merkel cell carcinoma.
- Matkowski R1, Lata E, Zietek M, Halon A, Forgacz J, Szynglarewicz B.
- The Journal of dermatological treatment.J Dermatolog Treat.2014 Oct;25(5):409-14. doi: 10.3109/09546634.2012.756969. Epub 2013 Aug 13.
- Herein, the authors describe the experience with the treatment of Merkel cell carcinoma (MCC) and review the literature regarding MCC treatment regimens. Nine patients underwent treatment due to stage I, II, or III MCC. The median follow up was 39 months. In five cases, tumors were excised with skin
- PMID 23216365
- Metastatic melanoma: results of 'classical' second-line treatment with cytotoxic chemotherapies.
- Perrin C1, Pracht M, Talour K, Adamski H, Cumin I, Porneuf M, Talarmin M, Mesbah H, Audrain O, Moignet A, Lefeuvre-Plesse C, Lesimple T.
- The Journal of dermatological treatment.J Dermatolog Treat.2014 Oct;25(5):396-400. doi: 10.3109/09546634.2012.697986. Epub 2012 Sep 2.
- BACKGROUND: Metastatic melanoma is one of the most aggressive tumours, with a median survival that does not exceed 12 months. None of the cytotoxic first-line therapies have shown survival benefit in randomised clinical trials.OBJECTIVE: To describe clinical benefit of second-line cytotoxic chemothe
- PMID 22632465
Japanese Journal
- 十二指腸より発生したEwing肉腫ファミリー腫瘍の1例
- 末梢神経未分化神経外胚葉性腫瘍と鑑別を要した原発性皮膚未分化大細胞リンパ腫の1例
Related Links
- Primitive neuroectodermal tumors (PNETs) are a group of highly malignant tumors composed of small round cells of neuroectodermal origin that affect soft tissue and bone. Primitive neuroectodermal tumors (PNETs) exhibit great diversity in their clinical manifestations and pathologic similarities with ...
- Primitive Neuroectodermal Tumors (PNETs) After leukemia and lymphoma, brain tumors are the most common type of childhood cancer. Primitive neuroectodermal tumors (PNETs) are malignant tumors of the central nervous system ...
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原始神経外胚葉性腫瘍
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