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Testicular Embryonal Carcinoma With Retroperitoneal Metastasis and Normal AFP and HCG: A Case Report
Panpan Teng1, Mingxi Yang1, Shang Song1
1Department of Urology Surgery, Tongren People's Hospital, Guizhou, China.
Case Reports in Oncological Medicine
|April 10, 2026
Summary
This case report details a testicular embryonal carcinoma in a young man with normal tumor markers, highlighting diagnostic challenges. Multidisciplinary approaches and long-term follow-up are crucial for such rare presentations.
Area of Science:
- Oncology
- Urology
Background:
- Testicular germ cell tumors are prevalent in young males.
- Embryonal carcinoma, a non-seminomatous subtype, typically presents with elevated serum tumor markers.
- Atypical presentations, like marker-negative cases, pose diagnostic difficulties.
Purpose of the Study:
- To report a rare case of testicular embryonal carcinoma with normal serum tumor markers.
- To emphasize the diagnostic challenges and the importance of a multidisciplinary approach in marker-negative cases.
- To underscore the efficacy of standard treatment protocols and long-term surveillance.
Main Methods:
- Case report of a 24-year-old male patient.
- Diagnostic workup included imaging, histopathology, and immunohistochemistry.
- Treatment involved radical orchiectomy and standard bleomycin, etoposide, and cisplatin (BEP) chemotherapy.
Main Results:
- The patient presented with testicular embryonal carcinoma and retroperitoneal lymph node metastasis despite persistently normal serum tumor markers.
- Diagnosis was confirmed via a combination of imaging, histopathology, and immunohistochemistry.
- The patient showed no recurrence at 12-month follow-up after treatment.
Conclusions:
- Accurate diagnosis of testicular embryonal carcinoma requires a multidisciplinary approach, especially in marker-negative cases.
- Established chemotherapy regimens like BEP are effective for this condition.
- Heightened clinical vigilance and extended follow-up are essential for managing atypical presentations.

