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Wilms’tumor develops from immature kidney cells and often presents as a painless abdominal mass, sometimes accompanied by abdominal swelling, blood in urine, fever, or high blood pressure. Although alarming, early detection significantly improves treatment outcomes.
Diagnosis is made through physical examination, imaging tests like ultrasound or CT scan, and biopsy if required.
Removing the affected kidney (nephrectomy) is often the first step, followed by additional therapies to target remaining cancer cells. With timely intervention, most children achieve excellent long-term survival rates.
Emotional and psychological support is also crucial for both children and families during treatment. Regular follow-up care helps monitor kidney function and prevent recurrence. Advancements in pediatric oncology continue to improve recovery and quality of life for young patients with Wilms’ tumor.