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Typically, testicular cancer develops in one or both testicles
in young men. It is a highly treatable and usually curable type of
cancer.
The testicles (also called the testes; a single testicle is
called a testis) are part of the male reproductive system. These 2
organs, each normally somewhat smaller than a golf ball in adult males,
are contained within a sac of skin called the scrotum, which hangs
beneath the base of the penis.
The testicles make the male hormone testosterone. They also
produce sperm. Sperm cells are carried from the testicle through the
vas deferens to the seminal vesicles, where they are mixed with a fluid
produced by the prostate gland. During ejaculation, sperm cells,
seminal vesicle fluid, and prostatic fluid enter the urethra, the tube
in the center of the penis through which both urine and semen leave the
body.

The testicles are made up of several types of cells, each of
which may develop into one or more types of cancer. It is important to
distinguish these types of cancers from one another because they differ
in the ways they are treated and in their prognosis (the course of the
disease and the outlook for survival).
Germ cell tumors
More than 90% of cancers of the testicle develop in special
cells known as germ cells. These are the cells that produce sperm.
There are 2 main types of germ cell tumors (GCTs) in men: seminomas and non-seminomas.
These 2 types occur about equally. Seminomas and non-seminomas cells
look very different when seen under a microscope.
Some cancers contain both non-seminoma and seminoma cells.
These are treated as non-seminomas because they grow and spread like
non-seminomas.
Seminomas
Seminomas develop from the sperm-producing germ cells of the
testicle. The 2 main subtypes of these tumors are classical (or
typical) seminomas and spermatocytic seminomas. Doctors can tell them
apart by how they look under the microscope.
Classical
seminoma: More than 95% of seminomas are classical. These
usually occur in men when they are between their late 30s and early
50s.
Spermatocytic
seminoma: This rare type of seminoma tends to occur in
older men. The average age of men diagnosed with spermatocytic seminoma
is about 55. Spermatocytic tumors tend to grow more slowly and are less
likely to spread to other parts of the body than classical seminomas.
Some seminomas can increase blood levels of a protein called
human chorionic gonadotropin (HCG). HCG can be detected by a simple
blood test and is considered a tumor marker for certain types of
testicular cancer. It can be used for diagnosis and to check for
response to therapy.
Non-seminomas
This type of germ cell tumor usually occurs in men between
their late teens and early 40s. There are 4 main types of non-seminoma
tumors:
- embryonal carcinoma
- yolk sac carcinoma
- choriocarcinoma
- teratoma
Most tumors are mixed with at least 2 different types, but
this does not change treatment. All non-seminoma germ cell cancers are
treated the same way.
Embryonal
carcinomas: This type of non-seminoma is present to some
degree in about 40% of testicular tumors, but pure embryonal carcinomas
occur only 3% to 4% of the time. When seen under a microscope, these
tumors can look like tissues of very early embryos. This type of
non-seminoma tends to grow rapidly and spread outside the testicle.
Embryonal carcinoma can increase blood levels of a tumor marker protein
called alpha-fetoprotein (AFP), as well as HCG.
Yolk sac
carcinomas: These are so named because their cells look
like the yolk sac of an early human embryo. Other names for this cancer
include yolk sac tumor, endodermal sinus tumor, infantile embryonal
carcinoma, or orchidoblastoma.
Yolk sac carcinoma is the most common form of testicular
cancer in children. When they occur in children, these tumors usually
are treated successfully. When yolk sac tumors develop in adults,
however, they are of more concern, especially if they are "pure" (that
is, the tumor does not contain other types of non-seminoma cells). Yolk
sac carcinomas respond very well to chemotherapy, even if they have
spread. This type of tumor almost always increases blood levels of AFP.
Choriocarcinomas:
This is a very rare and aggressive type of testicular cancer that
occurs in adults. These cancers are likely to spread rapidly to distant
organs of the body, including the lungs, bone, and brain. Pure
choriocarcinoma does not often occur in the testicles. More often,
choriocarcinoma cells are present with other types of non-seminoma
cells in a mixed germ cell tumor. This type of tumor increases blood
levels of HCG.
Teratomas:
Teratomas are germ cell tumors with areas that, when seen under the
microscope, look like each of the 3 layers of a developing embryo: the
endoderm (innermost layer), mesoderm (middle layer), and ectoderm
(outer layer). The 3 main types of these tumors are the mature
teratoma, immature teratoma, and teratoma with malignant
transformation. Pure teratomas do not increase AFP or HCG levels.
Mature teratomas
are tumors formed by cells similar to cells of adult tissues. They are
generally benign and rarely spread to nearby tissues and distant parts
of the body. They can usually be cured with surgery.
Sometimes deposits of mature teratoma are found after
chemotherapy to treat a non-seminomatous mixed germ cell tumor is
finished. These may be the part of a tumor that was left behind after
chemotherapy has killed the other components of the tumors. Some
experts believe that chemotherapy can change other types of
non-seminoma into teratoma.
Immature
teratomas are less well-developed cancers with cells that
look like those of an early embryo. Unlike mature teratomas, this type
is more likely to grow into (invade) surrounding tissues and to spread
(metastasize) outside the testicle. It can also sometimes recur (come
back) years after treatment.
Teratoma with
malignant transformation is a very rare cancer. These
cancers have some areas that look like mature teratomas but have other
areas where the cells have become a type of cancer that develops
outside of the testicle, in tissues such as muscles, glands of the
lungs or intestines, or the brain.
Carcinoma in situ
Testicular germ cell cancers may begin as a non-invasive form
of the disease called carcinoma
in situ (CIS) or intratubular
germ cell neoplasia. Carcinoma in situ may not always
progress to invasive cancer. Researchers have estimated that it can
take about 5 years for CIS to progress to the invasive form of germ
cell cancer.
It is hard to find CIS before it develops into invasive cancer
because it generally causes no symptoms and often does not form a lump
that you or the doctor can feel. The only way to diagnose testicular
carcinoma in situ is to have a biopsy. Some cases are found
incidentally (by accident) in men who have a testicular biopsy for some
other reason, such as infertility.
Experts don't agree about the best treatment for CIS. Since
CIS doesn't always become an invasive cancer, many doctors in this
country consider observation (watchful waiting) to be the best
treatment option.
When a testicular tumor like CIS becomes invasive, its cells
are no longer just in the seminiferous tubules (where sperm cells are
formed) but have grown into other structures of the testicle. These
cancer cells can then spread either to the lymph nodes (small,
bean-shaped collections of white blood cells that fight infection)
through lymphatic channels (fluid-filled vessels that connect the
series of lymph nodes), or through the blood circulation to other parts
of the body.
Stromal tumors
Tumors can also develop in the supportive and
hormone-producing tissues, or stroma, of the testicles. These tumors
are known as gonadal stromal tumors. They make up less than 5% of adult
testicular tumors but up to 20% of childhood testicular tumors. The 2
main types are Leydig cell tumors and Sertoli cell tumors.
Leydig cell
tumors: These generally benign tumors develop from the
Leydig cells in the testicle that normally produce male sex hormones
(androgens like testosterone). Leydig cell tumors can develop in both
adults (75% of cases) and children (25% of cases). They often produce
androgens but sometimes produce estrogens (female sex hormones).
Most Leydig cell tumors do not spread beyond the testicle and
are cured with surgery. Sometimes, however, these tumors do spread to
other parts of the body. If they do metastasize, Leydig cell tumors
have a poor prognosis because they usually do not respond well to
chemotherapy or radiation therapy.
Sertoli cell
tumors: These tumors develop from normal Sertoli cells,
which support and nourish the sperm-producing germ cells. Like the
Leydig cell tumors, they are usually benign. However, if they spread,
they tend to be resistant to chemotherapy and radiation therapy.
Secondary testicular tumors
Secondary testicular tumors are those that start in another
organ and then spread to the testicle. Lymphoma is the most common
secondary testicular cancer. Testicular lymphoma is more common than
primary testicular tumors in men older than 50. Their prognosis depends
on the type and stage of lymphoma. The usual treatment is surgical
removal, followed by radiation and/or chemotherapy. In boys with acute
leukemia, the leukemia cells can sometimes form a tumor in the
testicle.
Cancers of the prostate, lung, skin (melanoma), kidney, and
other organs also can spread to the testicles. The prognosis for these
cancers is usually poor because these cancers generally spread widely
to other organs as well. Treatment depends on the specific type of
cancer.
Last Medical Review: 08/03/2009 Last Revised: 08/03/2009
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