Glioblastoma multiforme classification: Difference between revisions
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==Classification== | ==Classification== | ||
Glioblastoma may be classified according to its origin into two subtypes: Primary and secondary.<ref name=ddd>Classification of glioblastoma multiforme. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/glioblastoma</ref> | Glioblastoma may be classified according to its origin into two subtypes: Primary and secondary.<ref name=ddd>Classification of glioblastoma multiforme. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/glioblastoma</ref> | ||
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! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|Differential diagnosis}} | |||
! style="background: #4479BA; width: 400px;" | {{fontcolor|#FFF|Characteristic features of the differential diagnosis}} | |||
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:[[Metastasis|Cerebral metastasis]] | |||
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*May look identical | |||
*Both may appear multifocal | |||
*Metastases are centred on grey-white matter junction and spare the overlying cortex | |||
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:[[Primary CNS lymphoma]] | |||
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*In patients with [[AIDS]] | |||
*Central [[necrosis]] is more common | |||
*Homogeneously enhancing on [[MRI]] | |||
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:[[Cerebral abscess]] | |||
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*Central restricted diffusion is helpful | |||
*[[Hemorrhagic]] then assessment may be difficult | |||
*Presence of smooth and complete SWI low intensity rim | |||
*Presence of dual rim sign | |||
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:[[Astrocytoma|Anaplastic astrocytoma]] | |||
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*No central [[necrosis]] | |||
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:[[Demyelination|Tumefactive demyelination]] | |||
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*Can appear similar | |||
*Open ring pattern of enhancement | |||
*Younger patients | |||
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:[[Stroke]] | |||
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*History is suggestive of diagnosis | |||
*No elevated choline | |||
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:[[Toxoplasmosis|Cerebral toxoplasmosis]] | |||
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*In patients with [[AIDS]] | |||
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:[[Radiation|Radiation necrosis]] | |||
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*History of [[radiation]] exposure | |||
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:[[Encephalitis]] | |||
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*History of [[fever]] | |||
*[[Confusion]] | |||
*[[Stiff neck]] may be present suggestive of [[meningoencephalitis]] | |||
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:[[Oligodendroglioma]] | |||
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*[[Biopsy]] helps in differentiation | |||
*Slower growing [[tumor]] | |||
*Better [[prognosis]] | |||
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:[[Epilepsy]] | |||
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*Multifactorial | |||
*Mass may or may not be observed on MRI depending on the cause | |||
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====Primary glioblastoma==== | ====Primary glioblastoma==== |
Revision as of 16:13, 16 September 2015
Glioblastoma multiforme Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Glioblastoma multiforme classification On the Web |
American Roentgen Ray Society Images of Glioblastoma multiforme classification |
Risk calculators and risk factors for Glioblastoma multiforme classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]
Overview
Glioblastoma may be classified into several subtypes based on its origin and molecular alterations.[1][2]
Classification
Glioblastoma may be classified according to its origin into two subtypes: Primary and secondary.[1]
Differential diagnosis | Characteristic features of the differential diagnosis |
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Primary glioblastoma
- De novo origin
- More aggressive
- Occurs in older patients
Secondary glioblastoma
- Arises from pre-existing lower grade gliomas
- Less aggressive
- Occurs in younger patients
Glioblastoma may be classified according to its molecular alterations into four subtypes:[2]
- Classic
- Proneural
- Mesenchymal
- Neural
References
- ↑ 1.0 1.1 Classification of glioblastoma multiforme. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/glioblastoma
- ↑ 2.0 2.1 Verhaak RG, Hoadley KA, Purdom E, Wang V, Qi Y, Wilkerson MD; et al. (2010). "Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1". Cancer Cell. 17 (1): 98–110. doi:10.1016/j.ccr.2009.12.020. PMC 2818769. PMID 20129251.