神経節細胞腫、神経節腫
- 関
- ganglioneuroma
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/11/29 15:47:20」(JST)
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Ganglioglioma |
Classification and external resources |
Dysplastic Cerebellar Ganglioglioma (Lhermitte-Duclos disease)
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ICD-O: |
M9505/1 |
MeSH |
D018303 |
Ganglioglioma is a tumour that arises from ganglion cells in the central nervous system.[1] Gangliogliomas and ganglioneuromas are slow growing benign tumors that mostly affect children and young adults.
Contents
- 1 Information
- 2 See also
- 3 References
- 4 External links
Information[edit]
The term "gangliocytoma" is sometimes equated with ganglioglioma. However, it is also sometimes equated with ganglioneuroma.[2] In this context, the glial nature of the tumor is de-emphasized. The term "gangliocytoma" is sometimes used to imply that the tumor is entirely neuronal.[3] While Gangliogliomas are most well known as occurring in the temporal lobe of the brain, they also occur in the frontal lobe, parietal lobe, occipital lobe, and regions of the thalamus and third ventricle. They also occur in the cerebellum and in the spinal cord. Gangliogliomas in the brain are often associated with seizures. They are the second most common cause of spinal cord tumors in children. They are usually either purely cystic or cystic with solid components, but may be solid. Calcification is frequently present and contrast enhancement on CT or MRI is variable. Because gangliogliomas are composed of both glial and neural elements, they may undergo malignant degeneration. When neuronal elements make up the majority of the mass, the neoplasm is referred to as a ganglioneuroma. In contrast, gangliocytomas are composed of mature ganglion cells and therefore have no potential for malignant change.[citation needed]
See also[edit]
References[edit]
- ^ "ganglioglioma" at Dorland's Medical Dictionary
- ^ "gangliocytoma" at Dorland's Medical Dictionary
- ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease. St. Louis, Mo: Elsevier Saunders. p. 1406. ISBN 0-7216-0187-1.
External links[edit]
- Ganglioglioma Images MedPix Medical Image Database
- Gangliocytoma Images MedPix Medical Image Database
- Lhermitte-Duclos Images MedPix Medical Image Database
Nervous tissue tumors/NS neoplasm/Neuroectodermal tumor (ICD-O 9350–9589) (C70–C72, D32–D33, 191–192/225)
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Endocrine/
Sellar (9350–9379) |
Sellar: Craniopharyngioma · Pituicytoma
Other: Pinealoma
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CNS
(9380–9539) |
Neuroepithelial
(brain tumors,
spinal tumors)
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Glioma
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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
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Oligodendroglioma
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Ependyma
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Ependymoma · Subependymoma
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Choroid plexus
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Choroid plexus tumor (Choroid plexus papilloma, Choroid plexus carcinoma)
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Multiple/unknown
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Oligoastrocytoma · Gliomatosis cerebri · Gliosarcoma
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Mature
neuron
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Ganglioneuroma: Ganglioglioma · Retinoblastoma · Neurocytoma · Dysembryoplastic neuroepithelial tumour · Lhermitte-Duclos disease
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PNET
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Neuroblastoma (Esthesioneuroblastoma, Ganglioneuroblastoma) · Medulloblastoma · Atypical teratoid rhabdoid tumor
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Primitive
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Medulloepithelioma
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Meningiomas
(Meninges)
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Meningioma · Hemangiopericytoma
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Hematopoietic
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Primary central nervous system lymphoma
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PNS: NST
(9540–9579) |
Cranial and paraspinal nerves: Neurofibroma (Neurofibrosarcoma, Neurofibromatosis) · Neurilemmoma/Schwannoma (Acoustic neuroma) · Malignant peripheral nerve sheath tumor
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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
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noco/auto/cong/tumr, sysi/epon, injr
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UpToDate Contents
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English Journal
- High Incidence of MYCN Amplification in a Moroccan Series of Neuroblastic Tumors: Comparison to Current Biological Data.
- Tabyaoui I, Tahiri-Jouti N, Serhier Z, El Maani K, Cherkaoui S, Al Zemmouri M, Othmani MB, Zamiati S.Source*Laboratory of Genetics and Molecular Pathology †Medical Informatics Laboratory, Faculty of Medicine and Pharmacy of Casablanca, Hassan II Aïn Chock University Departments of ‡Pediatrics III ∥Pediatric Visceral Surgery, Harouchi Children's Hospital §Department of Pediatric Oncology and Hematology, 20 Août 1953 Hospital ¶Pathology Department, Ibn Rochd Hospital, Casablanca, Morocco.
- Diagnostic molecular pathology : the American journal of surgical pathology, part B.Diagn Mol Pathol.2013 Jun;22(2):112-8. doi: 10.1097/PDM.0b013e318277448e.
- MYCN protooncogene status was assessed for the first time in Morocco in peripheral neuroblastic tumors, including neuroblastoma, ganglioneuroblastoma, and ganglioneuroma. Correlations with age at diagnosis, stage, mitosis-karyorrhexis index, differentiation, and Shimada histology were evaluated. Thi
- PMID 23628823
- Ganglioneuroma in the papilla of Vater with neurofibromatosis type 1: report of a case.
- Papp R, Baracs J, Papp A, Tornóczki T, Vincze A, Horváth OP, Kelemen D.SourceDepartment of Surgery, Medical Faculty of Pécs University, Rákóczi u. 2, 7623, Pécs, Hungary.
- Surgery today.Surg Today.2013 Jun;43(6):675-7. doi: 10.1007/s00595-012-0367-6. Epub 2012 Oct 7.
- Ganglioneuromas (GNs) are rare benign tumors and their association with neurofibromatosis type 1 (NF-1) is especially uncommon. We report in this article the case of a young woman, subjected to diagnostic work-up because of abdominal pain. Endoscopy and histology revealed not only a GN in the papill
- PMID 23052754
- Retroperitoneal Ganglioneuroma and Reversible Posterior Leukoencephalopathy in a Child With Acute Lymphoblastic Leukemia.
- Maher OM, Marco SA, Sadanandan S, Fireman F, Sedrak A.Source*Division of Pediatric Hematology and Oncology, The Brooklyn Hospital Center, Brooklyn, NY †National Cancer Institute, Cairo University, Cairo, Egypt.
- Journal of pediatric hematology/oncology.J Pediatr Hematol Oncol.2013 May 9. [Epub ahead of print]
- PMID 23669738
Japanese Journal
- 症例報告 閉塞性水頭症で発症したLhermitte-Duclos diseaseの一例
- F-22)Dysplastic gangliocytoma of the cerebellum(Lhermitte-Duclos disease)が疑われる小脳腫瘍の1例(F 中枢神経系腫瘍,2010年度小児腫瘍症例検討会)
- Gangliocytoma を合併したGH産生下垂体腺腫の1例
Related Links
- gangliocytoma /gan·glio·cy·to·ma/ (gang″gle-o-si-to?mah) ganglioneuroma. gan·gli·o·cy·to·ma (găng′glē-ō-sī-tō′mə) n. See ganglioneuroma. gangliocytoma [gang′glē·ō′sītō′mə] a benign tumor involving ganglion cells. These tumors are ...
- A gangliocytoma is related to a ganglioglioma. However, it only contains neural ganglion cells. It is a benign (WHO grade I) tumour. EpidemiologyThey account for 0.1-0.5% of all brain tumours and occur in children and young adults 2 ...
Related Pictures
★リンクテーブル★
[★]
- 英
- gangliocytoma, ganglioma, neuroganglioma
- 関
- 神経節神経腫、神経節細胞腫、神経節芽腫
- 同
- 神経細胞腫 neurocytoma、神経節性神経腫 ganglioneuroma
[★]
神経節腫、神経節神経腫、神経節性神経腫
- 関
- gangliocytoma
- 同
- 節神経腫
[★]
- 英
- gangliocytoma
- 関
- 神経節神経腫