Kidney cancer: Wikis

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Kidney cancer
Classification and external resources

Micrograph showing the most common type of kidney cancer (clear cell renal cell carcinoma). H&E stain.
MeSH D007680

Kidney cancer is usually defined as any cancer that is determined to have arisen from the kidney. It usually does not include metastatic cancer of the kidney, i.e. cancer that arose outside of the kidney and has spread to it.

The two most common types of kidney cancer, reflecting their location within the kidney, are renal cell carcinoma (RCC) and urothelial cell carcinoma (UCC) of the renal pelvis.

The distinction between these two types (RCC and UCC) is important because their prognosis, staging, and management, i.e. treatment (e.g. surgery, chemotherapy etc.), is different.

Contents

Types

Micrograph of a kidney cancer (chromophobe renal cell carcinoma, oncocytic variant), that may be challenging to differentiate from a benign kidney tumour (renal oncocytoma). H&E stain.
Micrograph of papillary renal cell carcinoma, a form of kidney cancer. H&E stain.

In addition to renal cell carcinoma and renal pelvis carcinoma, other, less common types of kidney cancer include:

Rarely, some other types of cancer and potentially cancerous tumors that more usually originate elsewhere can originate in the kidneys. These include:

Cancer in the kidney may also be secondary, the result of metastasis from a primary cancer elsewhere in the body.

Location within the kidney

Kidney cancer originate in the kidney in two principal locations: the renal tubule and the renal pelvis. Most cancers in the renal tubule are renal cell carcinoma and clear cell adenocarcinoma. Most cancers in the renal pelvis are transitional cell carcinoma.

Signs and symptoms

Common signs and symptoms of a kidney cancer include, in order of prevalence: palpable mass in the abdomen, hematuria, and hydronephrosis. However there may also be no signs or symptoms. A palpable mass is by far the most common sign.[5] The mass typically presents first in the anterior lumbar region, between the margins of the ribs and the crista ilii; it then grows forward to the umbilicus, upwards into the hypochondrium, and downwards into the iliac and inguinal regions. In extreme cases it fills the entire belly. The colon, and sometimes a portion of the small intestines, lies in front of it. This position of the colon furnishes an important diagnostic mark of all kidney cancers.[5]

Epidemiology

Around 208,500 new cases of kidney cancer are diagnosed in the world each year, accounting for just under 2% of all cancers.[6] The highest rates are recorded in Northern America and the lowest rates in Asian and African regions.[7]

In the United States in 2008, these two types together are estimated to cause 54,390 new cases and 13,010 deaths.[8]

2005. The most recent estimates of incidence of kidney cancer suggest that there are 63,300 new cases annually in the EU25. In Europe, kidney cancer accounts for nearly 3% of all cancer cases.[9]

In the UK kidney cancer is the eighth most common cancer in men, with 4,622 new cases diagnosed in 2005. This compares to 2,758 new cases of kidney cancer in women, giving a male:female ratio of 1.5:1. In women it is the fourteenth most common cancer. Male kidney cancer incidence rates increased by more than 85% from 7.1 per 100,000 in 1975 to 13.4 per 100,000 in 2005. In women the rates have more than doubled over the same period from 3.2 to 6.6 per 100,000. Most of the increase has occurred in older men and women, with rates more than doubling between 1975 and 2005 for men in their 70s and early 80 and women aged 65 and over.[10][11][12][13] Well over 50% of those diagnosed with kidney cancer in Britain will die as a result of the disease.

The incidence of kidney cancer is increasing also in the United States, and this increase is thought to be real, at least in part, not due only to changes in diagnostic practices.[14]

Some types of kidney cancer have a known hereditary or familial risk,[15] and to date five hereditary syndromes have been associated with renal cell carcinoma.[16]

Treatment

Treatment for kidney cancer depends on the type and stage of the disease.In wilms tumor,chemotherapy,radiotherapy,and nephrectomy are the accepted treatments.In renal cell carcinoma,treatment depends on the stage of the cancer,but typically does not involve chemotherapy and radiotherapy,as renal cell carcinoma is resistant to these therapies.Treatment for localized renal cell carcinoma consists of nephrectomy alone,with no adjuvant (post surgical) therapy.in metastatic renal cell carcinoma,treatment consists of targeted therapies such as torisel,nexavar,and sutent,the use of immunotherapy including interferon and interleukin-2,and in some cases,nephrectomy.other rare forms of kidney cancer,such as sarcomatoid renal carcinoma,are not disscussed here.</ref name="emedicine">"Error: no |title= specified when using {{Cite web}}". http://emedicine.medscape.com/article.  

In children

The majority of kidney cancers reported in children are Wilms' tumors. One study of 92 children with kidney masses reported 68 Wilms' tumor, 5 congenital mesoblastic nephroma, 4 clear cell sarcoma, 4 neuroblastoma, 4 renal cell carcinoma, 2 lymphoma, 2 angiomyolipoma, 1 teratoma, 1 hemangioma, and 1 renal epithelial tumor.[17]

See also

References

  1. ^ Thyavihally YB, Tongaonkar HB, Desai SB (September 2005). "Benign mixed epithelial stromal tumor of the renal pelvis with exophytic growth: case report". Int Semin Surg Oncol 2: 18. doi:10.1186/1477-7800-2-18. PMID 16150156. PMC 1215508. http://www.issoonline.com/content/2//18.  
  2. ^ Nzegwu MA, Aligbe JU, Akintomide GS, Akhigbe AO (May 2007). "Mature cystic renal teratoma in a 25-year-old woman with ipsilateral hydronephrosis, urinary tract infection and spontaneous abortion". Eur J Cancer Care (Engl) 16 (3): 300–2. doi:10.1111/j.1365-2354.2006.00755.x. PMID 17508953. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0961-5423&date=2007&volume=16&issue=3&spage=300.  
  3. ^ Chiu KC, Lin MC, Liang YC, Chen CY (2008). "Renal carcinosarcoma: case report and review of literature". Ren Fail 30 (10): 1034–9. doi:10.1080/08860220802403192. PMID 19016157. http://www.informaworld.com/openurl?genre=article&doi=10.1080/08860220802403192&magic=pubmed||1B69BA326FFE69C3F0A8F227DF8201D0.  
  4. ^ Kuroda N, Katto K, Tamura M, Shiotsu T, Hes O, Michal M, Nagashima Y, Ohara M, Hirouchi T, Mizuno K, Hayashi Y, Lee GH (January 2008). "Carcinoid tumor of the renal pelvis: consideration on the histogenesis". Pathol. Int. 58 (1): 51–4. doi:10.1111/j.1440-1827.2007.02188.x. PMID 18067641. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=1320-5463&date=2008&volume=58&issue=1&spage=51.  
  5. ^ a b William Roberts and Robert Maguire (1885). A practical treatise on urinary and renal diseases (4th ed.). Smith, Elder and Co.. pp. 697. http://books.google.com/books?pg=PA581&id=PoE5LAtmJqIC.  , page 581
  6. ^ Lindblad, P. and Adami H.O, Kidney Cancer, in Textbook of Cancer.
  7. ^ GLOBOCAN 2002, Cancer Incidence, Mortality and Prevalence Worldwide 2002 estimates. 2006.
  8. ^ "Kidney Cancer". National Cancer Institute, U.S. National Institutes of Health. http://www.cancer.gov/cancertopics/types/kidney. Retrieved 2009-03-03.  
  9. ^ Ferlay, J., et al., Estimates of the cancer incidence and mortality in Europe in 2006. Ann Oncol, 2007. 18(3): p. 581-92.
  10. ^ Office for National Statistics, Registrations of cancer diagnosed in 2005, England 2008.
  11. ^ Northern Ireland Cancer Registry, Registrations of cancer diagnosed in 2005, Northern Ireland 2008.
  12. ^ Information and Statistics Division, Scotland Registrations of cancer diagnosed in 2005, Scotland 2008.
  13. ^ Welsh Cancer Intelligence and Surveillance Unit, Registrations of cancer diagnosed in 2005, Wales 2008.
  14. ^ Lynch, Charles F.; West, Michele M.; Davila, Jessica A.; Platz, Charles E. (2007), "Chapter 24: Cancers of the Kidney and Renal Pelvis", in Ries, LAG; Young, JL; Keel, GE et al., SEER Survival Monograph: Cancer Survival Among Adults: US SEER Program, 1988-2001, Patient and Tumor Characteristics, SEER Program, NIH Pub. No. 07-6215, Bethesda, MD: National Cancer Institute, pp. 193–202, http://seer.cancer.gov/publications/survival  
  15. ^ Coleman JA (November 2008). "Familial and hereditary renal cancer syndromes". Urol. Clin. North Am. 35 (4): 563–72; v. doi:10.1016/j.ucl.2008.07.014. PMID 18992610. http://linkinghub.elsevier.com/retrieve/pii/S0094-0143(08)00071-2.  
  16. ^ Valladares Ayerbes M, Aparicio Gallego G, Díaz Prado S, Jiménez Fonseca P, García Campelo R, Antón Aparicio LM (November 2008). "Origin of renal cell carcinomas". Clin Transl Oncol 10 (11): 697–712. PMID 19015066.  
  17. ^ Miniati D, Gay AN, Parks KV, Naik-Mathuria BJ, Hicks J, Nuchtern JG, Cass DL, Olutoye OO (July 2008). "Imaging accuracy and incidence of Wilms' and non-Wilms' renal tumors in children". J. Pediatr. Surg. 43 (7): 1301–7. doi:10.1016/j.jpedsurg.2008.02.077. PMID 18639686. http://linkinghub.elsevier.com/retrieve/pii/S0022-3468(08)00271-6.  

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