| Literature DB >> 23639240 |
Ashley Walther1, Nicholas G Cost, Aaron P Garrison, James I Geller, Shumyle Alam, Gregory M Tiao.
Abstract
Renal rhabdomyosarcoma (RMS) is a rare pediatric tumor. Pancake kidneys are unusual anatomic anomalies resulting when both upper and lower poles of the embryonic kidney become fused. We report on a 4-year-old boy who was discovered to have a stage 4, group IV renal embryonal RMS arising from a pancake kidney with metastases to the lung, pelvis, and bone marrow. Treatment included multimodal therapy, consisting of neoadjuvant chemotherapy, complete surgical resection, and adjuvant chemotherapy. He remains in clinical remission 7 months after resection.Entities:
Mesh:
Year: 2013 PMID: 23639240 DOI: 10.1016/j.urology.2013.03.003
Source DB: PubMed Journal: Urology ISSN: 0090-4295 Impact factor: 2.649