Testicular cancer

Overview

Testicular cancer is a rare but highly treatable cancer that starts in the testicles, most commonly affecting men ages 15–35. Though uncommon, it’s the most frequent cancer in young men, with a 95%+ survival rate when caught early.

Risk factors include undescended testicle, family history, and previous testicular cancer. Symptoms may involve a painless lump, swelling, scrotal heaviness, or dull groin ache—often found during self-exam.

Diagnosis includes ultrasound, tumor marker blood tests, and imaging. Treatment typically involves surgical removal of the testicle, with radiation or chemotherapy used depending on the type (seminoma vs. non-seminoma) and stage.

Table of Contents

What Is Testicular Cancer?

Testicular cancer begins in the testicles (or testes), which are responsible for producing male hormones and sperm. Though relatively rare, it is the most common cancer in males ages 15 to 35.

Fortunately, testicular cancer is highly treatable, even when diagnosed at later stages.

2024 U.S. Statistics

Risk Factors

Most patients do not have a clear risk factor.

Common Symptoms

Many cases are discovered by self-exam. Regular monthly checks are encouraged.

Diagnosis

Types of Testicular Cancer

Treatment Options

Treatment depends on the type and stage, but typically includes:

Most men maintain full fertility and hormonal function, especially with early detection.

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