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Testicular Cancer
DefinitionTesticular cancer is a disease in which cancer cells are discovered in one or both testicles. The testicles, also known as testes or gonads, are located in a pouch beneath the penis called the scrotum. DescriptionThe testicles make up one portion of the male reproductive system. Normally, they are each somewhat smaller than a golf ball in size and are contained within the scrotum. The testicles are a man's primary source of male hormones, particularly testosterone. They also produce sperm. There are several types of cells contained in the testicles, and any of these may develop into one or more types of cancer. Over 90% of all testicular cancers begin in cells called germ cells. There are two main types of germ cell tumors in men: seminomas and nonseminomas. Seminomas make up about 40% of all testicular germ cell tumors. Nonseminomas make up a group of cancers, which include choriocarcinoma, yolk sac tumors, embryonal carcinoma, and teratoma. Although testicular cancer accounts for less then 2% of all cancers in men, it is the most commonly seen cancer in young men aged 15 to 35. It is also one of the most curable. The American Cancer Society estimates that approximately 8,980 new cases of testicular cancer will be diagnosed in American men in 2004. In addition, about 360 men will die of the disease during that year. Although the incidence of testicular cancer is rising, having doubled since 1975, it is still rare. Scandinavian countries have the highest rate in the world. Germany and New Zealand also have high rates. The lowest incidences of testicular cancer are in Asia and Africa. Causes and symptomsThe exact causes of testicular cancer are unknown. However, there is research showing that some men are more likely to acquire it than others. The risk for testicular cancer is much higher for boys born with one or both of their testicles located in the lower abdomen rather than in the scrotum. This condition is called cryptorchidism or undescended testicles. The lifetime risk of getting testicular cancer is four times higher for boys with cryptorchidism than the risk in the general population. This risk factor remains even if surgery is done to place the testicle back into the scrotum. Boys born with Down syndrome are also at higher risk of developing testicular cancer, although the reasons for this increased risk are not yet fully understood as of 2004. There are other risk factors as well. Men who have had abnormal development of their testicles are at increased risk, as are men with Klinefelter's syndrome (a disorder of the sex chromosomes). A family history of testicular cancer increases the possibility of getting the disease. Men infected with the human immunodeficiency virus (HIV), especially those with AIDS, have a higher incidence, as do infertile men. Certain testicular tumors appear more frequently among men who work in certain occupations, like miners, oil workers, and utility workers. There is no conclusive evidence that injuries to the testicles or environmental exposure to various chemicals cause the disease. Testicular cancer usually shows no early symptoms. It is suspected when a mass or lump is felt in the testes, although a testicular mass does not always indicate cancer and is usually painless. Symptoms:
DiagnosisWhen a man exhibits symptoms that suggest a possibility of testicular cancer, several diagnostic steps will occur before a definitive diagnosis is made. History and physicalThe physician takes a personal and family medical history and a complete physical examination is performed. The doctor will examine the scrotum as well as the abdomen and other areas to check for additional masses. Imaging studiesIf a mass is found, the physician will likely have an ultrasound performed. Through the use of sound waves, ultrasounds can help visualize internal organs and may be useful in telling the difference between fluid-filled cysts and solid masses. If the tumor is solid, it is most likely cancerous. Computed tomography as well as ultrasound may be used to diagnose malignant germ cell tumors in undescended testes. Blood testsCertain blood tests can be helpful in diagnosing some testicular tumors. Tumor markers are substances often found in higher-than-normal amounts in cancer patients. Some testicular cancers secrete high levels of certain proteins such as alpha-fetoprotein (AFP), human chorionic gonadotropin (HCG), and enzymes like lactate dehydrogenase (LDH). These markers may help find a tumor that is too small to be felt during a physical examination. In addition, these tests are also helpful in determining how much cancer is actually present, and in evaluating the response to treatment to make sure the tumor has not returned. SurgeryIf a suspicious growth is found, a surgeon will need to remove the tumor and send it to the laboratory for testing. A pathologist examines the testicular tissue microscopically to determine whether cancer cells are present. If cancer cells are found, the pathologist sends back a report describing the type and extent of the cancer. In almost all cases, the surgeon removes the entire affected testicle through an incision in the groin, though not through the scrotum. This procedure is called radical inguinal orchiectomy. Once testicular cancer is determined, further tests are necessary to find out if the cancer has metastasized (spread) to other parts of the body, and to ascertain the stage or extent of the disease. This information helps the doctor plan appropriate treatment. These tests may include computed tomography (CT scan), lymphangiography (x rays of the lymph system), bone scans, and chest x rays. TreatmentStagingOne method the cancer treatment team uses to describe the scope of a patient's cancer is the use of a staging system. Testicular cancer is classified using the TNM system. However, in order to simplify and summarize this information, the TNM description can be grouped according to stages. Stages of testicular cancer:
TreatmentThe treatment decisions for testicular cancer are dependent on the stage and cell type of the disease, as ![]() A cancerous growth on the testicle. (Illustration by Argosy Inc.) Surgery is normally the first line of treatment for testicular cancer and involves the removal of the affected testicle. This procedure is known as a radical inguinal orchiectomy. Depending on the type and stage of the cancer, some lymph nodes may also be removed at the same time, or possibly in a second operation. This procedure is called a retroperitoneal lymph node dissection, and can be a major operation. Some patients will experience temporary complications after surgery, including infections and bowel obstruction. If both of the testicles are taken out, a man will have no ability to produce sperm cells and will become infertile (unable to father a child). Surgery removing the lymph nodes may cause some damage to nearby nerves, which may interfere with the ability to ejaculate. Men undergoing surgery for testicular cancer may wish to discuss nerve-sparing surgery with their doctor, as well as sperm banking. Radiation therapy for testicular cancer is delivered from a machine and is known as external beam radiation. One potential problem with this type of radiation is that it can also destroy nearby healthy tissue as well as cancer cells. Other potential side effects include nausea, diarrhea and fatigue. A special device can be used to protect the unaffected testicle to preserve fertility. Chemotherapy refers to the use of drugs in treating cancer. Since the drugs enter the bloodstream and circulate throughout the body, chemotherapy is considered a systemic treatment. The drugs primarily used in the treatment of testicular cancer are cisplatin, vinblastine, bleomycin, cyclophosphamide, etoposide, and ifosfamide. These drugs are given in various combinations, since the use of two or more drugs is considered more effective than using only one drug. Since chemotherapy agents can affect normal as well as cancerous cells, several side effects are possible. These side effects include:
Several drugs are available to assist in treating these side effects, most of which will disappear after the treatment is completed. However, some of the chemotherapy agents used during treatment of testicular cancer may cause long-term side effects. These include hearing loss, nerve damage, and possible kidney or lung damage. Another potentially serious long-term complication is an increased risk of leukemia. This is a rare side effect, however, as it occurs in less than 1% of testicular cancer patients who receive chemotherapy. Chemotherapy may also interfere with sperm production. This may be permanent for some, but many will regain their fertility within a few years. Studies are ongoing to determine whether high doses of chemotherapy combined with stem-cell transplantation will prove effective in treating some patients with advanced testicular cancer. In this treatment, blood-forming cells called stem cells are taken from the patient (either from the bone marrow or filtered out of the patient's blood). These cells are kept frozen while high-dose chemotherapy is administered. After receiving the chemotherapy, the patient is given the stem cells through an infusion. This treatment enables the use of extra large doses of chemotherapy that might increase the cure rate for some testicular cancers. Preferred treatment plans by stage of diseaseStage I: Stage I seminomas are normally treated with a radical inguinal orchiectomy followed by radiation treatment aimed at the lymph nodes. More than 95% of Stage I seminomas are cured through this method. Another approach is to perform surgery only. Patients are then followed closely for several years with blood tests and imaging studies. If the cancer spreads later on, radiation or chemotherapy can still be used. Stage I non-seminomas are also highly curable with surgery, followed by one of three options. These options include the performance of a retroperitoneal lymph node dissection, two cycles of chemotherapy, or careful observation for several years. Stage II: Stage II seminomas and non-seminomas are cured in 90% to 95% of the cases. For the purposes of treatment, stage II testicular cancers are classified as either bulky or nonbulky. Nonbulky seminomas (no lymph nodes can be felt in the abdomen) are treated with an orchiectomy followed by radiation to the lymph nodes. Men with bulky seminomas have surgery, which may be followed by either radiation or a course of chemotherapy. Nonbulky Stage II non-seminomas are treated with surgery and lymph node removal, with possible chemotherapy. Men with bulky disease have surgery followed by chemotherapy. Stage III: Stage III seminomas and non-seminomas are treated with surgery followed by chemotherapy. This produces a cure in about 70% of the cases. Those who are not cured may be eligible to participate in clinical trials of other chemotherapy agents. Recurrent: Treatment of recurrent testicular cancer is dependent upon the initial stage and the treatment given. This might include further surgery and chemotherapy. Many men whose disease comes back after chemotherapy are treated with high-dose chemotherapy followed by bone marrow or stem cell transplantation. As of 2004, there is growing evidence that men treated with cisplatin for testicular cancer are at increased risk of coronary artery disease ten years or longer after treatment. In addition, men who have had an orchiectomy followed by external beam radiation therapy have a significantly increased risk of dying from heart disease or a second cancer. Key termsCryptorchidism — Occurs when a boy is born with one or both testicles in the lower abdomen rather than the scrotum. Known also as undescended testicles, it is the primary risk factor for testicular cancer. Metastatic testicular cancer — Testicular cancer that has spread to other parts of the body. Radical inguinal orchiectomy — Surgical procedure performed to remove one or both testicles. It is done via a groin incision. Testicles — Also called testes or gonads, they are part of the male reproductive system, and are located beneath the penis in the scrotum. Alternative treatmentThere are currently no scientifically proven alternative treatments known for testicular cancer. Nothing has been shown to be as successful as conventional treatment. However, some patients may find certain alternative or complementary treatments supportive while undergoing surgery, chemotherapy or radiation. For example, meditation and relaxation exercises may prove effective in reducing nausea and vomiting. Some dietary modifications and nutritional supplements may be helpful in assisting with recovery after surgery. The testicular cancer patient considering alternative treatments should talk it over with members of the cancer care team. They may be able to offer additional information. PreventionThe main risk factors associated with testicular cancer—cryptorchidism, family history of the disease, and being Caucasian—are unavoidable since they are present at birth. In addition, many men diagnosed with the disease have no known risk factors. Because of these reasons, it is not possible to prevent most incidences of testicular cancer. ResourcesBooksBeers, Mark H., MD, and Robert Berkow, MD., editors. "Testicular Cancer." In The Merck Manual of Diagnosis and Therapy. Whitehouse Station, NJ: Merck Research Laboratories, 2004. Nichols, Craig R., et al. "Neoplasms of the Testis." In Cancer Medicine. 5th ed. Hamilton, Ontario: American Cancer Society, 2000. PeriodicalsMercer, E. S., B. Broecker, E. A. Smith, et al. "Urological Manifestations of Down Syndrome." Journal of Urology 171 (March 2004): 1250-1253. Muttarak, M., W. C. Peh, and B. Chaiwun. "Malignant Germ Cell Tumours of Undescended Testes: Imaging Features with Pathological Correlation." Clinical Radiology 59 (February 2004): 198-2004. Nuver, J., A. J. Smit, D. T. Sleijfer, et al. "Microalbuminuria, Decreased Fibrinolysis, and Inflammation as Early Signs of Atherosclerosis in Long-Term Survivors of Disseminated Testicular Cancer." European Journal of Cancer 40 (March 2004): 701-706. Zagars, G. K., M. T. Ballo, A. K. Lee, and S. S. Strom. "Mortality after Cure of Testicular Seminoma." Journal of Clinical Oncology 22 (February 18, 2004): 640-647. OrganizationsAmerican Cancer Society. 1599 Clifton Road NE, Atlanta, GA 30329. (800) ACS-2345. http://www.cancer.org. National Cancer Institute. Cancer Information Service. (800) 4-CANCER. OtherAmerican Cancer Society (ACS). Cancer Facts & Figures 2004. http://www.cancer.org/downloads/STT/CAFF_finalPWSecured.pdf. Beeson, Dr. Debra. "Commentary: Testicular Cancer Commonly Seen in Younger Men." Cancer News. April 12, 2000. [cited June 19, 2001]. http://www.ontumor.com/cancernews_sm/testicular041200.htm. National Cancer Institute CancerNet. June 19, 2001. http://www.Cancernet.nci.nih.gov. The Testicular Cancer Resource Center. June 19, 2001. http://www.acor.org/TCRC.
testicular cancer, a malignant neoplastic disease of the testis occurring most frequently in men between 15 and 35 years of age. An undescended testicle is often involved. In many cases the tumor is detected after an injury, but trauma is not considered a causative factor. Patients with early testicular cancer are often asymptomatic, and metastases may be present in lymph nodes, the lungs, and the liver before the primary lesion is palpable. In the later stages there may be pulmonary symptoms, ureteral obstruction, gynecomastia, and an abdominal mass. Diagnostic measures include transillumination of the scrotum, excretory urography, lymphangiography, and a urine or serum test to evaluate circulating levels of tumor markers. Tumors develop more often in the right than in the left testis. Testis cancers are often curable. Chemotherapeutic agents, used in various combinations, are increasing the survival of patients with testicular cancer. Some of these drugs are actinomycin D, bleomycin, cis-platinum, cyclophosphamide, methotrexate, and vinCRIStine. Early detection by testicular self-examination enhances chances of cure. testicular cancer Lance Armstrong tumor, testicular malignancy, testicular neoplasia Oncology The most common cancer in ♂ age 20 to 35, which is curable if treated early; often first identified by its owner as a lump in the testicle,
usually noted after an episode of trauma Risk factors Hx of cryptorchidism, mumps orchitis, inguinal hernia during childhood, or previous TC on other side Management Orchiectomy, RT. See Embryonal carcinoma, Germ cell tumor, Seminoma, Testicular
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