Pheochromocytoma causes: Difference between revisions
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==Causes== | ==Causes== | ||
* Pheochromocytoma develops in called chromaffin cells, found in adrenal medulla. Chromaffin cells typically secrete adrenaline, noradrenaline and dopamine. These hormones are sympathetic stimulants. Pheochromocytoma results in the irregular and excessive release of these hormones causing hypertension and tachycardia. Approximately 10% are located in chromaffin tissue outside of the adrenal gland, The most common extradrenal locations are the abdomen and thorax | * Pheochromocytoma develops in called [[chromaffin cells]], found in adrenal medulla. Chromaffin cells typically secrete adrenaline, [[Norepinephrine|noradrenaline]] and [[dopamine]]. These hormones are sympathetic stimulants. Pheochromocytoma results in the irregular and excessive release of these hormones causing hypertension and tachycardia. Approximately 10% are located in chromaffin tissue outside of the adrenal gland, The most common extradrenal locations are the abdomen and thorax | ||
* Approximately 10% of tumors are malignant. Commonest sites of spread are base of skull, head and neck. | * Approximately 10% of tumors are malignant. Commonest sites of spread are base of skull, head and neck. | ||
* Genetic base of pheochromocytoma depends on 2 clusters: cluster 1 tumors are noradrenergic. Cluster 2 tumors are adrenergic.<sup>[[Pheochromocytoma pathophysiology#cite note-pmid23933153-3|[3]]]</sup> | * Genetic base of pheochromocytoma depends on 2 clusters: cluster 1 tumors are noradrenergic. Cluster 2 tumors are adrenergic.<sup>[[Pheochromocytoma pathophysiology#cite note-pmid23933153-3|[3]]]</sup> | ||
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* Succinate dehydrogenase (SDH) subunit genes | * Succinate dehydrogenase (SDH) subunit genes | ||
* Von Hippel-Lindau (VHL) disease | * [[Von Hippel-Lindau Disease|Von Hippel-Lindau (VHL) disease]] | ||
* Fumarate hydratase gene mutations | * Fumarate hydratase gene mutations | ||
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* '''Multiple endocrine neoplasia type 2A''' | * '''[[Multiple endocrine neoplasia type 2A]]''' | ||
* '''Multiple endocrine neoplasia type 2B''' | * '''[[Multiple endocrine neoplasia type 2B]]''' | ||
* '''Neurofibromatosis type 1 (NF1)''' | * '''[[Neurofibromatosis type 1|Neurofibromatosis type 1 (NF1)]]''' | ||
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Revision as of 17:40, 7 July 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Pheochromocytoma develops in called chromaffin cells, found in adrenal medulla which secrete adrenaline, noradrenaline.
Familial pheochromocytoma may be caused by a mutation of either VHL, RET, NF1, SDHB or SDHD genes.
Causes
- Pheochromocytoma develops in called chromaffin cells, found in adrenal medulla. Chromaffin cells typically secrete adrenaline, noradrenaline and dopamine. These hormones are sympathetic stimulants. Pheochromocytoma results in the irregular and excessive release of these hormones causing hypertension and tachycardia. Approximately 10% are located in chromaffin tissue outside of the adrenal gland, The most common extradrenal locations are the abdomen and thorax
- Approximately 10% of tumors are malignant. Commonest sites of spread are base of skull, head and neck.
- Genetic base of pheochromocytoma depends on 2 clusters: cluster 1 tumors are noradrenergic. Cluster 2 tumors are adrenergic.[3]
| Cluster 1 | Cluster 2 |
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