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Synchronous Acute Lymphoblastic Leukemia and Wilms Tumor: Report of a Case and Review of Previous Cases
Ariel M Strand1, Line W L Siggaard1, Peder S Wehner1
1Hans Christian Andersen Children's Hospital.
Background:
Multiple primary cancers are rare in pediatric patients and are mostly metachronous. Synchronous primary malignancies are exceedingly rare and pose significant challenges.
Observation:
This case report and review of previous cases focus on synchronous acute lymphoblastic leukemia (ALL) and Wilms tumor (WT). A systematic literature search identified 3 previous cases, confirming synchronous ALL and WT as a rare occurrence.
Conclusion:
Simultaneous primary cancers are rare and pose significant diagnostic and therapeutic challenges. Synchronous cancer warrants comprehensive genetic testing, although a genetic predisposition may not be identified. Reporting treatment strategies and outcomes adds to the knowledge regarding these rare cases.