Aggressive Multimodality Therapy for a Urachal Rhabdomyosarcoma - 14/07/22
Doi : 10.1016/j.urology.2022.04.009
N. Valeska Halstead 1, ⁎ 
, Nina Mikkilineni 1, Carrye R. Cost 2, Nicholas G. Cost 1
, Nina Mikkilineni 1, Carrye R. Cost 2, Nicholas G. Cost 1 1 University of Colorado Anschutz Medical Campus, Children's Hospital of Colorado, Division of Pediatric Urology, Aurora, CO
2 University of Colorado School of Medicine, Children's Hospital of Colorado, Department of Pediatric Hematology/Oncology/Bone Marrow Transplant, Aurora, CO
⁎Address correspondence to: N. Valeska Halstead, M.D., 12631 East 17th Ave, M/S C-319, Aurora, CO 80045.12631 East 17th Ave, M/S C-319AuroraCO80045.
Abstract |
Urachal rhabdomyosarcoma is a rare entity with a remarkably poor prognosis. Here we report on a 2-year-old male who presented with abdominal pain, fatigue, and urinary frequency. Imaging and subsequent surgical pathology confirmed urachal primary embryonal rhabdomyosarcoma. Our patient underwent upfront surgical resection with adjuvant chemoradiation per Children's Oncology Group protocol D9803. He is doing well 15 months after diagnosis.
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| Financial Disclosure: The authors declare that they have no relevant financial interests. |
© 2022
Elsevier Inc. Tous droits réservés.
Vol 165
P. e20-e24 - juillet 2022 Retour au numéro
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