Oligodendroglioma pathophysiology: Difference between revisions
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===Gross Pathology=== | ===Gross Pathology=== | ||
Common locations associated with oligodendroglioma include:<ref name=gross>Gross/radiologic findings of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref> | *Common locations associated with oligodendroglioma include:<ref name=gross>Gross/radiologic findings of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma</ref> | ||
:*[[Cerebral hemisphere]]s - most commonly [[frontal lobe]] (50-60%), followed by [[parietal lobe|parietal]] and [[temporal lobe]]s | |||
:*[[Posterior fossa]] (rare) | |||
:*[[spinal cord|Intramedullary spinal cord]] (very rare) | |||
*On gross pathology, oligodendroglioma is characterized by a well-circumscribed, gelatinous, and gray mass. | |||
They are generally composed of cells with small to slightly enlarged round nuclei with dark, compact nuclei and a small amount of eosinophilic cytoplasm. They are often referred to as "fried egg" cells due to their histologic appearance. They appear as a monotonous population of mildly enlarged round cells infiltrating normal brain parenchyma and producing vague nodules. Although the tumor may appear to be vaguely circumscribed, it is by definition a diffusely infiltrating tumor. | They are generally composed of cells with small to slightly enlarged round nuclei with dark, compact nuclei and a small amount of eosinophilic cytoplasm. They are often referred to as "fried egg" cells due to their histologic appearance. They appear as a monotonous population of mildly enlarged round cells infiltrating normal brain parenchyma and producing vague nodules. Although the tumor may appear to be vaguely circumscribed, it is by definition a diffusely infiltrating tumor. | ||
Revision as of 14:34, 7 October 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]
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Oligodendroglioma Microchapters |
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Diagnosis |
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Treatment |
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Oligodendroglioma pathophysiology On the Web |
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American Roentgen Ray Society Images of Oligodendroglioma pathophysiology |
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Risk calculators and risk factors for Oligodendroglioma pathophysiology |
Overview
Pathophysiology
Pathogenesis
- Oligodendroglioma does not arise from the bipotential oligodendrocytes, although tumor cells look very similiar.[1]
- Oligodendroglioma arises from the tripotential glial precursor cells.
Genetics
- Development of oligodendroglioma is the result from multiple genetic mutations.
- Genes associated with the pathogenesis of oligodendroglioma include:[2][3][4][5]
Gross Pathology
- Common locations associated with oligodendroglioma include:[6]
- Cerebral hemispheres - most commonly frontal lobe (50-60%), followed by parietal and temporal lobes
- Posterior fossa (rare)
- Intramedullary spinal cord (very rare)
- On gross pathology, oligodendroglioma is characterized by a well-circumscribed, gelatinous, and gray mass.
They are generally composed of cells with small to slightly enlarged round nuclei with dark, compact nuclei and a small amount of eosinophilic cytoplasm. They are often referred to as "fried egg" cells due to their histologic appearance. They appear as a monotonous population of mildly enlarged round cells infiltrating normal brain parenchyma and producing vague nodules. Although the tumor may appear to be vaguely circumscribed, it is by definition a diffusely infiltrating tumor.
Classically they tend to have a vasculature of finely branching capillaries that may take on a “chicken wire” appearance . When invading grey matter structures such as cortex, the neoplastic oligodendrocytes tend to cluster around neurons exhibiting a phenomenon referred to as “perineuronal satellitosis”. Oligodendrogliomas may invade preferentially around vessels or under the pial surface of the brain.
References
- ↑ General features of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma#cite_note-1
- ↑ Yip S, Butterfield YS, Morozova O, Chittaranjan S, Blough MD, An J; et al. (2012). "Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers". J Pathol. 226 (1): 7–16. doi:10.1002/path.2995. PMC 3246739. PMID 22072542.
- ↑ Molecular genetics of oligodendroglioma. https://en.wikipedia.org/wiki/Oligodendroglioma
- ↑ Bettegowda C, Agrawal N, Jiao Y, Sausen M, Wood LD, Hruban RH; et al. (2011). "Mutations in CIC and FUBP1 contribute to human oligodendroglioma". Science. 333 (6048): 1453–5. doi:10.1126/science.1210557. PMC 3170506. PMID 21817013.
- ↑ Prognosis and treatment of oligodendroglioma. Wikipedia 2015. https://en.wikipedia.org/wiki/Oligodendroglioma
- ↑ Gross/radiologic findings of oligodendroglioma. Libre Pathology. http://librepathology.org/wiki/index.php/Oligodendroglioma