Difference between revisions of "Paraganglioma"
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*[[WC]]: | *[[WC]]: | ||
**[http://commons.wikimedia.org/wiki/File:Carotid_body_tumour_2_intermed_mag.jpg Paraganglioma - intermed. mag. (WC)]. | **Carotid body tumour: | ||
**[http://commons.wikimedia.org/wiki/File:Carotid_body_tumour_2_high_mag.jpg Paraganglioma - high mag. (WC)]. | ***[http://commons.wikimedia.org/wiki/File:Carotid_body_tumour_2_intermed_mag.jpg Paraganglioma - intermed. mag. (WC)]. | ||
**[http://commons.wikimedia.org/wiki/File:Pheochromocytoma_high_mag.jpg Pheochromocytoma - high mag. (WC)]. | ***[http://commons.wikimedia.org/wiki/File:Carotid_body_tumour_2_high_mag.jpg Paraganglioma - high mag. (WC)]. | ||
**Duodenal paraganglioma - uncommon location: | |||
***[http://commons.wikimedia.org/wiki/File:Paraganglioma_-_low_mag.jpg Paraganglioma - low mag. (WC)]. | |||
***[http://commons.wikimedia.org/wiki/File:Paraganglioma_-_very_high_mag.jpg Paraganglioma - very high mag. (WC)]. | |||
***[http://commons.wikimedia.org/wiki/File:Paraganglioma_-_chromo_-_intermed_mag.jpg Paraganglioma - chromogranin A - intermed. mag. (WC)]. | |||
***[http://commons.wikimedia.org/wiki/File:Paraganglioma_-_s100_-_very_high_mag.jpg Paraganglioma - S100 - very high mag. (WC)]. | |||
**Other: | |||
***[http://commons.wikimedia.org/wiki/File:Pheochromocytoma_high_mag.jpg Pheochromocytoma - high mag. (WC)]. | |||
*www: | *www: | ||
**[http://path.upmc.edu/cases/case523.html Paraganglioma with gangliocytic differentiation - several images (upmc.edu)]. | **[http://path.upmc.edu/cases/case523.html Paraganglioma with gangliocytic differentiation - several images (upmc.edu)]. | ||
Revision as of 12:50, 20 May 2012
Paraganglioma is a rare tumour arising from the paraganglion. A paraganglioma arising in the adrenal gland is known as a pheochromocytoma.
General
- Definition: tumour of paraganglion.
- Can be sympathetic or parasympathetic.
- Most common paraganglioma = pheochromocytoma.[1]
- Head & neck most common site - after abdomen.
- Carotid body tumour = paraganglioma of carotid body.
Epidemiology
- Very rare
- Rarely malignant
- Familial syndromes assoc. with paragangliomas.[2]
- von Hippel Lindau.
- Hereditary paragangliomatosis.
- Neurofibromatosis type 1 (von Recklinghausen disease).
- MEN 2A.
- MEN 2B.
Clinical
- 10% bilateral, multiple, familial, pediatric and malignant.[3]
Gross
- Dusky colour.
Note:
- Pheo (in pheochromocytoma) is dusky; chromo is colour.
Image:
Microscopic
Features:[4]
- Zellballen - nests of cells - key low power feature.
- Zellballen is "cell balls" in German.
- Fibrovascular septae.
- Finely granular cytoplasm (salt-and-pepper nuclei).
- +/-Hemorrhage - very common.
DDx:
- Neuroendocrine tumour - nests surrounded by stroma/do not touch.
- Pheochromocytoma - paraganglioma of the adrenal gland.
Images:
- WC:
- Carotid body tumour:
- Duodenal paraganglioma - uncommon location:
- Other:
- www:
IHC
Features:[5]
- Chromogranin +ve.
- Synaptophysin +ve.
- S100 +/-.
- Cytokeratin -ve.
- EMA -ve.
- +ve in RCC.
EM
Features:[6]
- Neurosecretory granules.
- Electron dense core.
- Typically perinuclear location.
Image:
See also
References
- ↑ Thompson, Lester D. R. (2006). Endocrine Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 327. ISBN 978-0443066856.
- ↑ Thompson, Lester D. R. (2006). Endocrine Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 328. ISBN 978-0443066856.
- ↑ Thompson, Lester D. R. (2006). Endocrine Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 327. ISBN 978-0443066856.
- ↑ Thompson, Lester D. R. (2006). Endocrine Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 329-332. ISBN 978-0443066856.
- ↑ Thompson, Lester D. R. (2006). Endocrine Pathology: A Volume in Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 335. ISBN 978-0443066856.
- ↑ 6.0 6.1 URL: http://path.upmc.edu/cases/case408.html. Accessed on: 16 January 2012.