Ganglioneuroma pathophysiology: Difference between revisions
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==Pathophysiology== | ==Pathophysiology== | ||
===Genetics=== | |||
===Gross Pathology=== | ===Gross Pathology=== | ||
*Ganglioneuromas are solid, firm [[tumors]] that are typically white when seen with the naked eye | *Ganglioneuromas are solid, firm [[tumors]] that are typically white when seen with the naked eye | ||
Revision as of 14:42, 9 September 2015
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Ganglioneuroma Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Ganglioneuroma pathophysiology On the Web |
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American Roentgen Ray Society Images of Ganglioneuroma pathophysiology |
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Risk calculators and risk factors for Ganglioneuroma pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]
Overview
Pathophysiology
Genetics
Gross Pathology
- Ganglioneuromas are solid, firm tumors that are typically white when seen with the naked eye
- Gangliocytoma is commonly located in the following regions:[1]
- Posterior paraspinal mediastinum (most common)
- Adrenal gland
- Paraspinal retroperitoneum
- Neck
Microscopic Pathology
- Ganglioneuromas are derived from the primordial neural crest cells, which are undifferentiated cells of the sympathetic nervous system.
- Ganglioneuromas are fully differentiated neuronal tumors that do not contain immature elements.
- They are composed of ganglion cells, schwann cells and fibrous tissue.
Videos
{{#ev:youtube|IWng6E9flDA}}
Associated Conditions
- Multiple endocrine neoplasia type IIb: particularly with mucosal ganglioneuromas.[1]
- Turner syndrome
- Neurofibromatosis type 1
References
- ↑ 1.0 1.1 Pathology of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma