Undescended Testicle: Risk for Testicular Cancer
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Being born with an
		undescended testicle increases the risk for
		testicular cancer.
- The risk is about 4 to 10
		  times greater in males who have an undescended testicle than in other
		  males.footnote 1
- The higher up in the path of
		  descent a testicle stops, the more likely it is to form a tumor. An
		  undescended testicle in the belly is 4 to 6 times more likely to develop
		  cancer than one that is farther down toward the
		  scrotum.
Moving the testicle to the scrotum may help reduce the
		risk of cancer. Most
		doctors recommend surgery to place undescended testicles in the scrotum. This makes it much easier to find cancer if it does develop.
 Untreated undescended testicles are usually
		  removed in adult men and teens who have gone through
		  puberty because of the increased risk of
		  cancer.
Men who have an undescended testicle
		should have regular medical checkups (at least once every 2 years) throughout
		life. These checkups may include a testicular exam. If you have an undescended
		testicle, talk with your doctor about how often you need to be checked.
Some doctors recommend a testicular biopsy during surgery to correct an
		undescended testicle if the testicle is in the belly
		or the child has genital defects, such as
		hypospadias, or a
		genetic disorder. In this test, a small sample of
		tissue is taken from the testicles and examined to find out the potential for
		developing cancer.
References
Citations
- Braga LHP, Bagli DJ (2011). Urologic abnormalities of the genitourinary tract. In CD Rudolph et al., eds., Rudolph's Pediatrics, 22nd ed., pp. 1741-1748. New York: McGraw-Hill.
Credits
ByHealthwise Staff
Primary Medical ReviewerJohn Pope, MD - Pediatrics
Adam Husney, MD - Family Medicine
Specialist Medical ReviewerPeter Anderson, MD, FRCS(C) - Pediatric Urology
Current as of:
                May 5, 2017
Braga LHP, Bagli DJ (2011). Urologic abnormalities of the genitourinary tract. In CD Rudolph et al., eds., Rudolph's Pediatrics, 22nd ed., pp. 1741-1748. New York: McGraw-Hill.