Testicular Cancer

Types of Cancer

What is Testicular Cancer?

Cancer that starts in the testicles is called testicular cancer. To understand this cancer, it helps to know about the typical structure and function of the testicles.

What are testicles?

Testicles (also called testes; a single testicle is called a testis) are part of the male reproductive system. The two organs are each usually a little smaller than a golf ball in adult males. They’re held within a sac of skin called the scrotum. The scrotum hangs under the base of the penis.

Testicles have two main functions:

  • They make male hormones (androgens) such as testosterone.
  • They produce sperm, the male cells needed to fertilize a female egg cell to start a pregnancy.

Sperm cells are made in long, thread-like tubes inside the testicles called seminiferous tubules. They’re then stored in a small coiled tube behind each testicle called the epididymis.

During ejaculation, sperm cells are carried from the epididymis through the vas deferens to the seminal vesicles. They mix with fluids made by the vesicles, prostate gland, and other glands to form semen. This fluid then enters the urethra, the tube in the centre of the penis through which both urine and semen leave the body.

Types of testicular cancer

The testicles are made up of many types of cells, each of which can develop into one or more cancer types. It’s essential to know the kind of cell cancer started in and what kind of cancer it is because they differ in how they’re treated and their prognosis (outlook). Doctors can tell the type of testicular cancer you have by looking at the cells under a microscope.

Germ cell tumours

More than 90% of cancers of the testicle start in cells known as germ cells. These are the cells that make sperm. The main types of germ cell tumours (GCTs) in the testicles are seminomas and non-seminomas.

These types occur about equally. Many testicular cancers contain both seminoma and non-seminoma cells. These mixed germ cell tumours are treated as non-seminomas because they grow and spread like non-seminomas.


Seminomas tend to grow and spread more slowly than non-seminomas. The two main subtypes of these tumours are classical (or typical) seminomas and spermatocytic seminomas.

  • Classical seminoma: More than 95% of seminomas are classical. These usually occur in men between 25 and 45.
  • Spermatocytic seminoma: This rare type of seminoma tends to occur in older men. (The average age is about 65.) Spermatocytic tumours 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 checked with a simple blood test and is considered a tumour marker for certain testicular cancer types. It can be used for diagnosis and to check how the patient is responding to treatment.


These types of germ cell tumours usually occur in men between their late teens and early 30s. The four main types of non-seminoma tumours are embryonal carcinoma, yolk sac carcinoma, choriocarcinoma, and teratoma. Most tumours are a mix of different types (sometimes with seminoma cells, too), but this doesn’t change the treatment of most non-seminoma cancers.

Embryonal carcinoma: These cells are found in about 40% of testicular tumours, but pure embryonal carcinomas occur only 3% to 4% of the time. When seen under a microscope, these tumours can look like tissues of very early embryos. This type of non-seminoma tends to increase and spread outside the testicle. Embryonal carcinoma can increase blood levels of a tumour marker protein called alpha-fetoprotein (AFP), as well as human chorionic gonadotropin (HCG).

Yolk sac carcinoma: These tumours are so named because their cells look like the early human embryo’s yolk sac. Other names for this cancer include yolk sac tumour, endodermal sinus tumour, infantile embryonal carcinoma, or orchidoblastoma. This is the most common form of testicular cancer in children (especially in infants), but pure yolk sac carcinomas (tumours that do not have other types of non-seminoma cells in them) are rare in adults.

When they occur in children, these tumours usually are treated successfully. But they’re of more concern when they occur in adults, especially if they are pure. Yolk sac carcinomas respond very well to chemotherapy, even if they have spread. This type of tumour almost always increases blood levels of AFP (alpha-fetoprotein).

Choriocarcinoma: This is a scarce and fast-growing type of testicular cancer in adults. Pure choriocarcinoma is likely to spread rapidly to other parts of the body, including the lungs, bones, and brain. Choriocarcinoma cells are often seen with different types of non-seminoma cells in a mixed germ cell tumour. These mixed tumours tend to have a somewhat better outlook than pure choriocarcinomas, although the presence of choriocarcinoma is always a worrisome finding. This type of tumour increases blood levels of HCG (human chorionic gonadotropin).

Teratoma: Teratomas are germ cell tumours with areas that, under a microscope, look like each of the three layers of a developing embryo: the endoderm (innermost layer), mesoderm (middle layer), and ectoderm (outer layer). Pure teratomas of the testicles are rare and do not increase AFP (alpha-fetoprotein) or HCG (human chorionic gonadotropin) levels. Most often, teratomas are seen as parts of mixed germ cell tumours.

There are three main types of teratomas:

  • Mature teratomas are tumours formed by cells a lot like the cells of adult tissues. They rarely spread and can usually be cured with surgery, but some come back after treatment.
  • Immature teratomas are less well-developed cancers with cells that look like those of an early embryo. This type is more likely than a mature teratoma to grow into (invade) nearby tissues, spread (metastasize) outside the testicle, and come back years after treatment.
  • Teratomas with somatic type malignancy are very rare. These cancers have some areas that look like mature teratomas but have other places where the cells have become a type of cancer that usually develops outside the testicle (such as a sarcoma, adenocarcinoma, or even leukemia).

Carcinoma in situ of the testicle

Testicular germ cell cancers can start as a non-invasive form of the disease called carcinoma in situ (CIS) or intratubular germ cell neoplasia. In testicular CIS, the cells look abnormal under the microscope, but they have not yet spread outside the seminiferous tubules’ walls (where sperm cells are formed). Carcinoma in situ doesn’t always progress to invasive cancer.

It’s hard to find CIS before it becomes invasive cancer because it generally doesn’t cause symptoms or form a lump that you or the doctor can feel. The only way to diagnose testicular CIS is to have a biopsy. (This is a procedure to take out a tiny bit of tissue so it can be checked under a microscope.) Sometimes CIS is found incidentally (by accident) when a testicular biopsy is undertaken for another reason, such as infertility.

Experts disagree about the best treatment for CIS. Since CIS doesn’t always become invasive cancer, many doctors worldwide consider observation (watchful waiting) to be the best treatment option.

When CIS of the testicle becomes invasive, its cells are no longer just in the seminiferous tubules, they’ve 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) through lymphatic vessels (tiny fluid-filled tubes that connect the lymph nodes) or through the blood to other parts of the body.

Stromal tumours

Tumours can also start in the supportive and hormone-producing tissues, or stroma, of the testicles. These tumours are known as gonadal stromal tumours. They make up less than 5% of adult testicular tumours but up to 20% of childhood testicular tumours. The main types are Leydig cell tumours and Sertoli cell tumours.

Leydig cell tumours

These tumours start in the Leydig cells in the testicle that typically make male sex hormones (androgens like testosterone). Leydig cell tumours can develop in both adults and children. These tumours often produce androgens (male hormones), but sometimes they make estrogens (female sex hormones).

Most Leydig cell tumours are not cancer (benign). They seldom spread beyond the testicle and can often be cured with surgery. Still, a small number of Leydig cell tumours do spread to other parts of the body. These tend to have a poor outlook because they usually don’t respond well to chemo or radiation therapy.

Sertoli cell tumours

These tumours start in normal Sertoli cells, which support and nourish the sperm-making germ cells. Like the Leydig cell tumours, these tumours are usually benign. But if they spread, they typically don’t respond well to chemo or radiation therapy.

Secondary testicular cancers

Cancers that start in another organ and then spread (metastasize) to the testicle are called secondary testicular cancers. These are not true testicular cancers – they don’t start in the testicles. They’re named and treated based on where they started.

Lymphoma is the most common secondary testicular cancer. Testicular lymphoma is more common in men older than 50 than primary testicular tumours. The outlook 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 tumour in the testicle. Along with chemotherapy to treat leukemia, this might require radiation or surgery to remove the testicle.

Cancers of the prostate, lung, skin (melanoma), kidney, and other organs also can spread to the testicles. The prognosis for these cancers tends to be inadequate because these cancers have usually spread widely to other organs. Treatment depends on the specific type of cancer.