Merck Manual

Please confirm that you are a health care professional

honeypot link

Urethral Cancer


J. Ryan Mark

, MD, Sidney Kimmel Cancer Center at Thomas Jefferson University

Last full review/revision Sep 2019| Content last modified Sep 2019
Click here for Patient Education

Urethral cancer is rare and occurs in both sexes; it may be squamous or transitional cell carcinoma or, occasionally, adenocarcinoma.

Most patients are aged 50. Certain strains of human papillomavirus have been implicated in certain cases. Urethral tumors invade adjacent structures early and thus tend to be advanced when diagnosed. External groin or pelvic (obturator) lymph nodes are usually the first sites of metastasis.

Symptoms and Signs

Most women present with hematuria and obstructive voiding symptoms or urinary retention. Most have a history of urinary frequency or urethral syndrome (hypersensitivity of the pelvic floor muscles). Most men present with symptoms of urethral stricture; only a few present with hematuria or a bloody discharge. Sometimes if the tumor is advanced, a mass is felt.


  • Cystourethroscopy

Diagnosis is suggested clinically and confirmed by cystourethroscopy. Biopsy may be required to differentiate urethral carcinoma, prolapse, and caruncle. CT or MRI is used for staging.


Prognosis depends on the precise location in the urethra and extent of the cancer, particularly depth of invasion. The 5-year survival rates are > 60% for patients with distal tumors and 10 to 20% for patients with proximal tumors. Recurrence rate is >50%.


  • Usually excision or ablation

For superficial or minimally invasive distal tumors in the anterior urethra, treatment is with surgical excision, radiation therapy (interstitial or a combination of interstitial and external beam), fulguration, or laser ablation. Larger and more deeply invasive anterior tumors and proximal tumors in the posterior urethra require multimodal therapy with radical surgery and urinary diversion, usually in combination with chemotherapy and radiation therapy. Surgery includes bilateral pelvic and sometimes inguinal lymph node dissection, often with removal of part of the symphysis pubis and inferior pubic rami.

Click here for Patient Education
NOTE: This is the Professional Version. CONSUMERS: Click here for the Consumer Version
Professionals also read

Test your knowledge

Fanconi Syndrome
Fanconi syndrome can be hereditary or acquired. Hereditary Fanconi syndrome usually accompanies another genetic disorder. Of these accompanying disorders, which of the following is most common? 
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID
Download the Manuals App iOS ANDROID

Also of Interest