Abstract
Background: Rhabdomyosarcoma (RMS) and Neuroblastoma (NB) are highly malignant soft tissue sarcoma with tendency to metastasize. Due to the similarities in clinical manifestations and imaging features between RMS and NB, they are often misdiagnosed, which resulted in improper treatment progression of the mass. On the other hand, the treatment paradigm for patients with metastasis RMS/NB and non-metastasis RMS/ NB is different.
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