Pediatric Primary Yolk Sac Tumour of the Kidney: Recommendations for Pretreatment Diagnosis

Abstract

Introduction Although nephroblastomas are frequently treated without prior biopsy, there are the occasional other pediatric renal tumors that require different management. In the literature, there are around 30 primary renal germ cell tumors (GCT), including four cases of Yolk sac tumor (YST). We present another primary renal YST.Case report: A five-year-old boy was diagnosed as Wilms tumor on radiology and needle biopsy. He received chemotherapy, with no response. The post-chemotherapy resection specimen revealed a YST.Conclusion: Renal YST may be indistinguishable from Wilms tumor clinically and radiologically. For pre-biopsy chemotherapy management protocols, serum tumor markers such as AFP may be recommended to identify the occasional GCT, including YST. Pre-chemotherapy needle biopsies may lead to misdiagnosis, and may require confirmation by an experienced pathologist or central review.

Keywords:

• Extragonadal
• germ cell tumor
• renal tumor
• yolk sac tumor
• nephroblastoma

Disclosure statement

No conflicts of interest to declare.

Additional information

Funding

The authors received no financial support for the publication of this article.