Management of Testicular Atrophy Identified on Radiograph
In patients with testicular atrophy identified on imaging, perform testicular ultrasound to confirm atrophy (volume <12 ml), assess for underlying pathology including malignancy, and strongly consider contralateral testis biopsy to evaluate for testicular intraepithelial neoplasia (TIN), particularly in high-risk patients (age <40 years, atrophic testis, or extragonadal germ cell tumor). 1, 2
Initial Diagnostic Workup
Imaging Confirmation
- Scrotal ultrasound is mandatory to confirm testicular atrophy, define testicular volume, characterize any masses, and evaluate the contralateral testis 3, 2
- Testicular volume <12 ml defines atrophy and warrants comprehensive evaluation 1, 2
- Look specifically for solid masses, heterogeneous echogenicity, or suspicious features that would indicate malignancy 3, 4
Laboratory Assessment
- Measure serum tumor markers (AFP, β-HCG, LDH) to screen for occult germ cell tumors 1, 4, 2
- Obtain hormonal evaluation including total testosterone, LH, and FSH to assess testicular function 2
- Complete metabolic panel if malignancy is suspected 4
Risk Stratification for Malignancy
High-Risk Features Requiring Aggressive Management
Patients with testicular atrophy have significantly elevated risk of testicular cancer and TIN, particularly when combined with: 1, 2
- Age <40 years with testicular volume <12 ml: ~30% risk of contralateral TIN 1
- History of cryptorchidism (undescended testis) 4, 2
- Extragonadal germ cell tumor 1
- Family history of testicular cancer 3
- Synchronous or metachronous contralateral testicular cancer (2-5% risk) 1
Contralateral Testis Biopsy Decision
- Strongly consider biopsy in patients with atrophic testis (<16 ml), especially if age <40 years 1, 2
- The European Germ Cell Cancer Consensus Group notes that while routine biopsy is not universally indicated, it should be performed in high-risk scenarios 1
- If biopsy is performed and TIN is diagnosed, management options include surveillance, orchiectomy, or radiotherapy (20 Gy in 2 Gy fractions) 1
Management Based on Clinical Context
If Atrophic Testis with Normal Contralateral Testis
- Orchiectomy is preferred over radiotherapy to eliminate cancer risk and avoid scattered radiation damage to the healthy contralateral testis 1
- This is particularly appropriate when the atrophic testis is non-functional 1
- Consider fertility preservation (sperm banking) before any intervention 1, 2
If Bilateral Atrophy or Solitary Testis
- Organ-preserving surgery may be considered in experienced centers if a small tumor is identified 1, 2
- Mandatory postresection testicular radiotherapy (20 Gy) is required, which renders tissue azoospermic but preserves some testosterone production 1
- Sperm cryopreservation must be discussed before any intervention 1, 2
If TIN Diagnosed in Setting of Planned Chemotherapy
- Postpone definitive TIN treatment until after chemotherapy, as cisplatin-based chemotherapy eradicates TIN in approximately two-thirds of patients 1
- Consider re-biopsy no earlier than 6 months post-chemotherapy to assess for persistent TIN 1
- This avoids excessive Leydig cell damage from combined chemotherapy and radiation 1
Testosterone Monitoring and Replacement
- Regular testosterone monitoring is essential after radiotherapy or organ-preserving surgery, as both can impair Leydig cell function 1
- Offer hormone replacement therapy to all patients with subnormal testosterone levels and clinical signs of androgen deficiency 1
- Long-term follow-up is necessary to monitor for hypogonadism 2
Surveillance Protocol
For Patients with Atrophic Testis Under Observation
- Teach testicular self-examination due to increased malignancy risk 3, 2
- Regular monitoring of hormone levels and testicular volume 2
- Maintain high index of suspicion for development of solid masses 3
If Orchiectomy Performed for Malignancy
- Follow-up depends on histology and stage with specific protocols for seminoma versus non-seminoma 4
- Post-chemotherapy patients require clinical review, chest X-ray, and tumor markers every 2 months for year 1, every 3 months for year 2, then every 6 months to 5 years 1
Critical Pitfalls to Avoid
- Never delay evaluation of testicular atrophy with suspicious features—delayed diagnosis correlates with higher stage at presentation 4
- Never perform scrotal approach for suspected testicular tumors, as this increases local recurrence risk; always use inguinal approach 4
- Never overlook fertility preservation before definitive treatment in reproductive-age men 1, 2
- Do not assume benign etiology in atrophic testis—the increased cancer risk persists throughout life, particularly with cryptorchidism history 2, 5
- Avoid routine biopsy for isolated testicular microlithiasis without other risk factors, as this alone does not increase malignancy risk 3