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What causes testicular cancer?
The causes of testicular cancer and reasons for the recent
increase in frequency in some countries are unknown. Exposure to female
hormones in the environment, in water (possibly from the oral contraceptive
pill in water supplies) has been suggested. Undescended testicles (in which one
or both testicles stay inside the body after birth and never sit in the
scrotum) are a major risk factor. Men with one or both testicles undescended
have a greatly increased risk - 1 in 44 will develop testicular cancer. Your
risk increases if your father or brother suffered from testicular
cancer.
What are the types of testicular tumour?
The term 'germ cell' is applied to cells that are capable of
developing into sperm (in the male) or eggs (in the female). Thus the general
term 'germ cell tumours' basically means tumours of either the testicle or the
ovary.
There are two main types of testicular tumour - seminomas and non-seminomatous germ cell tumours (NSGCT, often also called 'teratomas'). The two types are about equally common. Seminomas are fairly smooth tumours but teratomas are more complex and may contain different types of tissue.
Both types of tumour are capable of producing hormones (or proteins) that are detectable in the blood. Human chorionic gonadotrophin (hCG) is produced by both teratomas and seminomas (hCG is the hormone produced by a woman during pregnancy, and is what is detected in a pregnancy test). Teratomas can produce alpha-fetoprotein (AFP). Often the level of these proteins in the blood is useful in the diagnosis, treatment and follow-up of men who have had testicular cancer.
How is testicular cancer treated?
Testicular cancer can be cured in about 96 per cent of cases if
caught at an early stage. Even when these tumours spread, they can still be
cured in 80 per cent of cases, and large tumours can be cured in 60 per cent of
cases. Late diagnosis increases the risk of a poorer response to
treatment.
Seminomas are usually diagnosed before they have spread to other parts of the body (metastasised) and radiotherapy (X-ray treatment) is the treatment of choice. If the seminoma has spread, then either radiotherapy or radiotherapy plus chemotherapy (anticancer medicine) is used. The original tumour and testicle is removed surgically.
With teratomas, provided there is no evidence of spread on examination and scans, and blood tests show none of the protein markers then a closely-observed 'wait and see' policy can be taken following tumour removal. If there is any sign of recurrence then chemotherapy may be started.
One of the great successes of modern chemotherapy has been the treatment of germ cell tumours. Usually four courses are given, at three-weekly intervals, of bleomycin, etoposide and cisplatin (BEP).
Where there are remaining tumours following chemotherapy (for example within the lymph nodes - the commonest site for the tumour to spread first) these are removed surgically in the case of teratomas. In seminomas they can be observed, and usually will not cause further trouble.
Although the affected testicle is removed during treatment, an artificial testicle (prosthesis) can be inserted to disguise the fact almost completely. Treatment with radiotherapy or chemotherapy can affect the ability to father children but in many cases fertility is not affected. Sperm can be stored before treatment for later use.