What is Pediatric Oncology Surgery?
Pediatric oncology surgery is a specialized field focused on the surgical diagnosis, staging, and treatment of childhood cancers. Cancer in children differs significantly from adult cancers in types, behavior, and treatment response. Our fellowship-trained pediatric surgeons at Western Surgical Group work as integral members of multidisciplinary pediatric oncology teams, collaborating closely with pediatric oncologists, radiation oncologists, radiologists, pathologists, and other specialists to provide comprehensive cancer care.
The surgeon’s role in treating childhood cancer is multifaceted: obtaining tissue for accurate diagnosis through biopsy, surgically removing tumors when possible, placing long-term venous access devices for chemotherapy delivery, performing “second-look” surgeries to assess treatment response, managing cancer-related complications, and providing ongoing surgical support throughout the child’s cancer journey. Our approach emphasizes complete tumor removal when achievable while preserving organ function and minimizing long-term effects on growth and development.
While a cancer diagnosis is devastating for families, it’s important to know that childhood cancers often respond very well to treatment. Survival rates for many pediatric cancers now exceed 80-90% thanks to advances in treatment protocols. We’re committed to providing expert surgical care while supporting children and families through this challenging experience with compassion, clear communication, and coordination with the entire care team.
Multidisciplinary Approach to Pediatric Cancer
- Pediatric oncologists (cancer specialists)
- Radiation oncologists
- Pediatric radiologists
- Pathologists specializing in pediatric tumors
- Pediatric anesthesiologists
- Genetic counselors
- Social workers and child life specialists
- Pediatric intensive care teams
This collaborative approach ensures your child receives comprehensive, coordinated care based on the latest treatment protocols.
Types of Pediatric Tumors We Treat
Neuroblastoma: The most common cancer in infants, arising from nerve tissue. Can occur anywhere along the sympathetic nervous system but most commonly in the adrenal glands or abdomen. Treatment involves surgery to remove the tumor, often combined with chemotherapy and sometimes radiation. Prognosis varies significantly based on age at diagnosis, tumor stage, and genetic factors.
Wilms Tumor (Nephroblastoma): The most common kidney cancer in children, typically affecting children ages 3-4. Treatment involves surgical removal of the affected kidney (nephrectomy), usually after chemotherapy to shrink the tumor. Most children with Wilms tumor have excellent outcomes, with cure rates exceeding 90% for favorable histology tumors.
Hepatoblastoma: A rare liver cancer affecting young children, usually under age 5. Treatment involves chemotherapy followed by surgical removal of the tumor, which may require removing a portion or majority of the liver. The liver’s remarkable ability to regenerate allows for extensive resection when necessary. Prognosis depends on tumor stage and whether complete surgical removal is possible.
Soft Tissue Sarcomas (Rhabdomyosarcoma): Cancers arising from muscle or connective tissue that can occur anywhere in the body. Treatment is multimodal, typically combining surgery, chemotherapy, and sometimes radiation. The surgical approach depends on tumor location and size, with the goal of complete removal while preserving function.
Germ Cell Tumors: Tumors arising from reproductive cells, occurring in the ovaries, testes, or along the midline of the body. Types include teratomas (which can be benign or malignant), yolk sac tumors, and other variants. Treatment depends on tumor type, location, and whether it’s benign or malignant. Many germ cell tumors have excellent cure rates.
Adrenal and Pancreatic Tumors: Rare tumors of these organs requiring specialized surgical expertise. Treatment depends on tumor type but often involves surgical removal when possible.
Thoracic Malignancies: Including pleuropulmonary blastoma (a rare lung cancer), bronchial carcinoid tumors, and chest wall Ewing’s sarcoma. Treatment typically involves surgical resection combined with chemotherapy and sometimes radiation.
Melanoma: While less common in children than adults, pediatric melanoma does occur and requires surgical removal with appropriate margins, possible lymph node evaluation, and close follow-up.
Lympho-vascular Malformations: While often benign, some vascular tumors can behave aggressively and require surgical intervention as part of comprehensive treatment.
Surgical Procedures in Pediatric Oncology
Diagnostic Biopsy: Obtaining tissue samples for pathologic diagnosis, which is essential before starting cancer treatment. Biopsies may be performed using needle techniques, laparoscopically, or through open surgery depending on tumor location.
Tumor Resection: Surgical removal of the cancer, aiming for complete resection with negative margins (no cancer cells at the edges of removed tissue) while preserving organ function when possible.
Central Venous Access Placement: Inserting long-term intravenous catheters (Port-a-Cath or Broviac/Hickman catheters) for chemotherapy administration, blood draws, and supportive care, avoiding repeated needle sticks.
Second-Look Surgery: Evaluating treatment response and removing residual tumor after chemotherapy or radiation therapy.
Metastasectomy: Removing cancer that has spread to other locations like lungs or liver when isolated metastases are present and complete removal is feasible.
Why Pediatric Surgical Expertise Matters in Cancer Care
- Understanding of pediatric tumor biology and behavior
- Specialized techniques for operating on small bodies and delicate tissues
- Knowledge of growth and development considerations
- Experience with pediatric cancer treatment protocols
- Minimally invasive approaches when appropriate
- Focus on long-term outcomes and quality of life
- Coordination with pediatric oncology teams
What to Expect
The pediatric cancer journey typically begins with diagnostic workup including imaging studies (CT, MRI, PET scans), laboratory tests, and often biopsy. Once cancer is diagnosed, your child’s case will be discussed at a multidisciplinary tumor board where specialists collaborate to develop an individualized treatment plan based on tumor type, stage, location, and your child’s overall health.
Surgical timing depends on the specific cancer. Some tumors are removed first (upfront resection), while others are treated with chemotherapy first to shrink the tumor before surgery (neoadjuvant therapy). Hospital stays vary from outpatient for simple biopsies or port placement to a week or more for major tumor resections. Recovery depends on the extent of surgery and your child’s overall condition.
Throughout treatment, we maintain close communication with families, explaining each step, addressing concerns, and supporting you through this difficult journey. Our goal is not just cancer cure but also minimizing treatment effects and supporting your child’s quality of life during and after cancer therapy.

