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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people.

Renal Tumours

Renal tumours may occur in adults or in children but the pathology is different.

Renal tumours of childhood

Wilms' tumour is thought to arise from embryonic renal tissue. It is by far the most common renal tumour of childhood, accounting for more than 90% of renal tumours under the age of 20.1 It was first described by the German surgeon Max Wilms at the end of the 19th century.
Other are:

  • Renal carcinoma (5.4%)
  • Clear cell sarcoma (1.6%)
  • Rhabdoid tumour of the kidney (0.9%)

Renal tumours of adults

Renal cell carcinoma is the commonest of the tumours of the kidney in adults, accounting 70% of all renal tumours, and 85% of renal cancers. Benign tumours of the kidney are rare. Renal cell carcinomas arise from the proximal tubule cells. Its old name of hypernephroma reflects that it was believed to arise from adrenal gland.
Renal cell carcinoma comprises which can be broken down into:

  • Clear cell (70%)
  • Chromophil (eosinophil, basophil) (15%)
  • Chromophobe (5%)
  • Collecting duct carcinoma (2%)
  • Renal oncocytoma (5%)

The other 3% comprise:

  • Transitional cell carcinoma
  • Wilms' tumour
  • Angiomyolipoma- commonly seen in patients with tuberous sclerosis
  • Leiyomyosarcoma
  • Sarcoma
  • Adenoma- frequently found as an incidental finding at post mortem, if diagnosed during life treated with partial nephrectomy due to histological similarity to adenocarcinoma.

Epidemiology
  • Renal tumours account for approximately 2% of all malignancies.
  • Males are more likely to be affected than females with a ratio of 2:1.2.
  • More than 6,600 people are diagnosed with kidney cancer each year in the UK2 and there are around 3,600 deaths.3
  • The peak age of incidence for renal carcinoma is 60 to 80 years old.
  • Several risk factors have been identified including smoking, obesity, hypertension, long term dialysis and Von Hippel Lindau syndrome.
  • Occupations associated with an increased risk include workers exposed to cadmium or asbestos and coke oven workers in the iron and steel industries.4
  • Hereditary renal cancers tend to be multiple, bilateral and occur at an earlier age than others.5
  • Wilms' tumour affects about 1 in 100,000 children before the age of 15. In 5 to 10% of cases it is bilateral.

Risks for renal cell carcinoma are discussed more fully in the article on the subject.

Renal tumours may be benign or malignant, primary or secondary. Primary tumours may arise from the cells of the renal parenchyma, or from the transitional cell lining of the collecting ducts. The most common primary renal tumour in adults is renal carcinoma and this tumour accounts for approximately 2% of all newly diagnosed cancers in the UK. In children, Wilm's tumour is the most common and this tumour is the most common intra-abdominal tumour in children.

Presentation

Children

  • Abdominal mass
  • Loin pain
  • Haematuria
  • Hypertension, gross haematuria, and fever are observed in 5 to 30% of patients

Adults

  • Haematuria
  • Loin pain
  • Abdominal mass
  • Recurrent fever
  • Hypertension
  • Oedema
  • Today, more than 50% of adult renal tumours are detected when using ultrasound to investigate non-specific features.6 The most common of these are: hypertension, cachexia, weight loss, pyrexia, neuromyopathy, amyloidosis, elevated ESR, anaemia, abnormal LFTs, hypercalcaemia and polycythaemia.7
  • 25 to 30% of patients present with symptoms of metastatic disease.7

In children a mass may be found but in adults there is often no abnormality on examination. Both renal cell carcinoma and Wilms' tumour metastasise to lung and bones.

Differential diagnosis

The differential diagnosis will depend upon the presentation. There are articles on abdominal mass, loin pain and gross haematuria that will discuss the various causes.

Staging

Staging of adult tumours is the Robson classification:
The Robson classification is as follows:

  • Stage 1 is confined to the kidney.
  • Stage 2 extends to the adrenal gland or perinephric tissues.
  • Stage 3a extends into the renal vein or vena cava.
  • Stage 3b involves the regional nodes.
  • Stage 3c involves both regional nodes and the renal vein or vena cava.
  • Stage 4a tumours extend beyond the Gerota fascia.
  • Stage 4b has distant metastases.

A slightly more complex TNM system is used and recommended by the European Guidelines.7

For Wilms' tumour:

  • Stage 1 The tumour is confined to the kidney.
  • Stage 2 The tumour has begun to spread beyond the kidney to nearby structures.
  • Stage 3 The tumour has spread beyond the kidney, and either there are lymph node metastases or it cannot be completely removed by surgery
  • Stage 4 There is metastatic spread, usually to the lungs, liver, bone or brain.
  • Stage 5 Bilateral Wilms' tumour.

See also separate Renal Cell Carcinoma and Wilms' Tumour articles.

Management, prognosis and prevention

See separate Renal Cell Carcinoma and Wilms' Tumour articles - linked in "Investigations" above.


Document references
  1. National Cancer Institute (USA); Childhood Renal Tumors
  2. UK kidney cancer statistics, Cancer Research UK
  3. UK kidney cancer mortality statistics, Cancer Research UK
  4. Kidney cancer risk factors, Cancer Research UK (website)
  5. Choyke PL, Glenn GM, Walther MM, et al; Hereditary renal cancers. Radiology. 2003 Jan;226(1):33-46. [abstract]
  6. Vallancien G, Torres LO, Gurfinkel E, et al; Incidental detection of renal tumours by abdominal ultrasonography. Eur Urol. 1990;18(2):94-6. [abstract]
  7. Guidelines on renal cell carcinoma, European Association of Urology (2007)

Internet and further reading Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2008.
DocID: 2722
Document Version: 22
DocRef: bgp686
Last Updated: 10 Jan 2008
Review Date: 9 Jan 2010

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest.

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