A rare case of Botryoid Wilms’ tumor
Published in the World Journal of Surgical Oncology, the authors report a case of botryoid Wilms’ tumor, a 4-year-old boy, who presented with a chief complaint of dysuria and gross hematuria.

The computed tomography and radical nephroureterectomy showed that a botryoid sarcoma-like appearance occupied the right renal pelvis and extended into the bladder. Histologic examination further confirmed this case was a mixed type of Wilms’ tumor.

The tumor extended from the renal pelvis into the ureter and bladder, then some degenerative and necrotic tissue with calcification discharged from urethra. Postoperative adjuvant chemotherapy was executed. At 24-month follow-up, there was no evidence of recurrence.

Read in detail about the case here: https://pxmd.co/7NKYU