Renal cell carcinoma causes: Difference between revisions
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==Causes== | ==Causes== | ||
Sporadic development of renal cell carcinomas contributes to the majority of cases of the most common renal cell carcinoma, the conventional (or clear cell) carcinoma.<ref name="pmid24359990">{{cite journal |vauthors=Haas NB, Nathanson KL |title=Hereditary kidney cancer syndromes |journal=Adv Chronic Kidney Dis |volume=21 |issue=1 |pages=81–90 |date=January 2014 |pmid=24359990 |pmc=3872053 |doi=10.1053/j.ackd.2013.10.001 |url=}}</ref><ref name="pmid20448661">{{cite journal |vauthors=Linehan WM, Srinivasan R, Schmidt LS |title=The genetic basis of kidney cancer: a metabolic disease |journal=Nat Rev Urol |volume=7 |issue=5 |pages=277–85 |date=May 2010 |pmid=20448661 |pmc=2929006 |doi=10.1038/nrurol.2010.47 |url=}}</ref> | Sporadic development of renal cell carcinomas contributes to the majority of cases of the most common renal cell carcinoma, the conventional (or clear cell) carcinoma.<ref name="pmid24359990">{{cite journal |vauthors=Haas NB, Nathanson KL |title=Hereditary kidney cancer syndromes |journal=Adv Chronic Kidney Dis |volume=21 |issue=1 |pages=81–90 |date=January 2014 |pmid=24359990 |pmc=3872053 |doi=10.1053/j.ackd.2013.10.001 |url=}}</ref><ref name="pmid20448661">{{cite journal |vauthors=Linehan WM, Srinivasan R, Schmidt LS |title=The genetic basis of kidney cancer: a metabolic disease |journal=Nat Rev Urol |volume=7 |issue=5 |pages=277–85 |date=May 2010 |pmid=20448661 |pmc=2929006 |doi=10.1038/nrurol.2010.47 |url=}}</ref><ref name="pmid23038766">{{cite journal |vauthors=Linehan WM |title=Genetic basis of kidney cancer: role of genomics for the development of disease-based therapeutics |journal=Genome Res. |volume=22 |issue=11 |pages=2089–100 |date=November 2012 |pmid=23038766 |pmc=3483538 |doi=10.1101/gr.131110.111 |url=}}</ref> | ||
The following tables show the sporadic and hereditary renal-cell carcinomas and associated causes: | The following tables show the sporadic and hereditary renal-cell carcinomas and associated causes: | ||
Latest revision as of 15:20, 10 December 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Farima Kahe M.D. [2]
Overview
The causes of renal cell carcinoma include von hippel-lindau (VHL), hereditary paragangliomas, leiomyomatosis, birt-hogg-dube syndrome, and several other genetic factors.
Causes
Sporadic development of renal cell carcinomas contributes to the majority of cases of the most common renal cell carcinoma, the conventional (or clear cell) carcinoma.[1][2][3]
The following tables show the sporadic and hereditary renal-cell carcinomas and associated causes:
Sporadic Forms of Renal Cell Carcinoma
| Histologic Appearance | Incidence | Gene | Frequency |
| Conventional (Clear Cell) | 75 | VHL | 60 % |
| Papillary | 12 | MET TFE3 |
13 % < 1 % |
| Chromophobe | 4 | ||
| Oncocytoma | 4 | ||
| Collecting Duct | < 1 | ||
| Unclassified | 3 - 5 |
Hereditary Forms of Renal Cell Carcinoma
| Syndrome | Associated Gene | Common Histological Appearance |
| VHL Disease | VHL | Conventional (Clear Cell) |
| FCRC | Chromosome 3p translocation | Conventional (Clear Cell) |
| Hereditary Paraganglioma | SDHB | Conventional (Clear Cell) |
| HPRC | MET | Papillary |
| HLRCC | FH | Papillary |
| Birt-Hogg-Dube Syndrome | BHD | Chromophobe / Oncocytoma |
References
- ↑ Haas NB, Nathanson KL (January 2014). "Hereditary kidney cancer syndromes". Adv Chronic Kidney Dis. 21 (1): 81–90. doi:10.1053/j.ackd.2013.10.001. PMC 3872053. PMID 24359990.
- ↑ Linehan WM, Srinivasan R, Schmidt LS (May 2010). "The genetic basis of kidney cancer: a metabolic disease". Nat Rev Urol. 7 (5): 277–85. doi:10.1038/nrurol.2010.47. PMC 2929006. PMID 20448661.
- ↑ Linehan WM (November 2012). "Genetic basis of kidney cancer: role of genomics for the development of disease-based therapeutics". Genome Res. 22 (11): 2089–100. doi:10.1101/gr.131110.111. PMC 3483538. PMID 23038766.
- ↑ 4.0 4.1 Cohen HT, McGovern FJ (2005). "Renal-cell carcinoma". N Engl J Med. 353 (23): 2477–90. doi:10.1056/NEJMra043172. PMID 16339096.