What is the appropriate treatment for a 23-year-old male with a 3 cm testicular mass suspicious for testicular cancer based on ultrasonography?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 13, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Treatment of a 3 cm Testicular Mass Suspicious for Testicular Cancer

The appropriate treatment for a 23-year-old male with a 3 cm testicular mass suspicious for testicular cancer on ultrasonography is radical inguinal orchiectomy, which should be performed as the primary management. 1

Initial Evaluation

Before proceeding with treatment, the following steps are essential:

  • Obtain serum tumor markers (STM) including alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), and lactate dehydrogenase (LDH) prior to any treatment, including orchiectomy 1
  • Scrotal ultrasound with Doppler has already been performed, showing a hypoechoic mass, which is highly suggestive of malignancy 1
  • Counsel the patient about the risks of hypogonadism and infertility 1
  • Offer sperm banking before orchiectomy, especially important in this young patient 1, 2

Primary Treatment

  • Radical inguinal orchiectomy is the standard of care for a 3 cm testicular mass suspicious for cancer 1, 3
  • The procedure should be performed through an inguinal incision with early vascular control at the internal inguinal ring 1
  • Any scrotal violation for biopsy or open surgery should be avoided as it may lead to tumor seeding 1
  • The timing of orchiectomy should be prompt but not emergent unless there are signs of life-threatening metastatic disease 1

Considerations for Testis-Sparing Surgery

Testis-sparing surgery (TSS) is generally not recommended for this patient with a 3 cm mass for several reasons:

  • TSS is only considered for highly selected patients with masses <2 cm, and this patient has a 3 cm mass 1
  • TSS is primarily considered for patients with:
    • Equivocal ultrasound/physical exam findings and negative tumor markers 1
    • Congenital, acquired, or functionally solitary testis 1
    • Bilateral synchronous tumors 1

Post-Orchiectomy Management

After orchiectomy, the following steps are crucial:

  • Repeat serum tumor markers (AFP, hCG, LDH) at appropriate half-life intervals to establish nadir levels for staging and risk stratification 1
  • Perform staging imaging studies:
    • CT scan of abdomen and pelvis with IV contrast or MRI abdomen and pelvis without and with IV contrast 1
    • Chest X-ray (for seminoma) or CT chest with IV contrast (for non-seminoma) 1

Subsequent Treatment Based on Staging

Treatment after orchiectomy depends on histology, stage, and risk classification:

  • Stage I (confined to testis): Options include active surveillance, adjuvant chemotherapy, or retroperitoneal lymph node dissection (for non-seminoma) or radiation therapy (for seminoma) 2, 4
  • Stage II (retroperitoneal lymph node involvement): Treatment typically involves chemotherapy and/or retroperitoneal lymph node dissection 2
  • Stage III (distant metastases): Chemotherapy based on the International Germ Cell Cancer Collaborative Group (IGCCCG) risk stratification 1

Important Considerations and Pitfalls

  • Avoid scrotal approach for orchiectomy as it increases risk of local recurrence and altered lymphatic drainage 1
  • Be aware that retroperitoneal hematoma can occur post-orchiectomy and may mimic metastatic disease on imaging 5
  • Monitor for potential complications of treatment, including:
    • Infertility (sperm banking should be offered before treatment) 1, 2
    • Hypogonadism requiring testosterone replacement 1
    • Cardiovascular complications in long-term survivors 4, 6

Prognosis

With appropriate treatment, testicular cancer has excellent outcomes:

  • 5-year survival rates are approximately 99% for stage I, 92% for stage II, and 85% for stage III disease 2
  • Treatment at high-volume centers with multidisciplinary expertise may improve outcomes 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Management of Primary Testicular Tumor.

The Urologic clinics of North America, 2019

Research

Testicular Cancer: Diagnosis and Treatment.

American family physician, 2018

Research

Retroperitoneal hematoma following radical orchiectomy: Two cases.

Canadian Urological Association journal = Journal de l'Association des urologues du Canada, 2017

Research

Diagnosis and treatment of testicular cancer.

American family physician, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.