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Wilms’ Tumor Surgery: An Overview

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Over time, considerable progress has been made in identifying and managing Wilms tumors, especially in surgical treatment.

Medically reviewed by

Dr. A.k. Tiwari

Published At April 23, 2024
Reviewed AtApril 23, 2024

Introduction:

Nephroblastoma, another name for Wilms tumor, is the most frequent renal cancer in children, accounting for over 95% of all kidney cancers in pediatric patients. This embryonal tumor of the kidney usually appears in children between the ages of two and five years old, with a small preference for females. Genetic susceptibility and specific congenital defects have been linked to its development. However, the precise cause is still unknown.

The mainstay of treatment for Wilms tumors is surgery, which aims to minimize long-term consequences and preserve renal function in addition to completely removing the tumor. The process has revolutionized with the introduction of minimally invasive procedures and nephron-sparing therapies, improving patient outcomes and decreasing morbidity for pediatric patients.

What Are the Surgical Management Options for Wilms Tumor?

The main objective of surgical therapeutic options for Wilms tumors is usually total tumor removal while maintaining renal function. These options consist of:

  • Nephrectomy: The most popular surgical treatment for Wilms tumors is nephrectomy. It entails removing the tumor in addition to the damaged kidney. A total nephrectomy, which involves removing the entire kidney, or a partial nephrectomy, which involves removing the tumor while leaving part of the kidney intact, may be necessary, depending on the severity of the disease and the existence of bilateral tumors.

  • Lymph Node Dissection: Lymph nodes in the surrounding area may be sampled or dissected to check for tumor dissemination in situations where there is a suspicion of lymph node involvement or metastasis.

  • Surgical debulking: This procedure involves removing as much of the tumor as feasible when it cannot be fully removed because of its size or involvement of nearby structures. Additional treatment options, such as chemotherapy or radiation therapy, may then be used.

  • Biopsy: Although a biopsy is not usually the first surgical choice for treating a Wilms tumor, it may be done in some circumstances to confirm the diagnosis, particularly if imaging tests are not clear or the tumor is incurable.

What Are the Advances in Wilms Tumor Surgery?

Pediatric patients' prognosis and morbidity have greatly improved as a result of advancements in Wilms tumor surgery.

Among the noteworthy developments are:

  • Nephron-sparing Surgery: Nephron-sparing techniques have become more popular as awareness of the significance of maintaining renal function has grown. By removing the tumor while keeping as much healthy kidney tissue as possible, partial nephrectomy techniques lower the risk of long-term renal consequences such as hypertension and chronic kidney disease.

  • Minimally Invasive Surgery: The area of pediatric oncology, particularly Wilms tumor surgery, has undergone a revolution thanks to the development of laparoscopic and robotic-assisted surgical procedures. Compared to traditional open surgery, minimally invasive techniques have advantages like fewer incisions, less blood loss, shorter hospital stays, and quicker recovery times. These methods enable precise tumor removal with the least amount of tissue stress, which makes them especially useful in certain situations.

  • Neoadjuvant Chemotherapy: It is used more often as a preoperative treatment for Wilms tumors. Chemotherapy before surgery can help reduce the size of the tumor, which can facilitate surgical resection and lessen the amount of surgery needed. It has been demonstrated that using this strategy will enhance surgical results and raise the possibility of attaining total tumor excision.

  • Surgical Planning and Imaging: Preoperative planning and intraoperative navigation for Wilms tumor surgery have been improved by developments in imaging modalities such as computed tomography (CT) and magnetic resonance imaging (MRI). By accurately assessing the size, position, and involvement of surrounding tissues in a tumor, high-resolution imaging aids in surgical decision-making and improves surgical results.

  • Multidisciplinary Care: To treat Wilms tumors completely, pediatric surgeons, oncologists, radiologists, pathologists, and other experts must work together. To maximize results and reduce treatment-related problems, multidisciplinary tumor boards provide tailored treatment planning incorporating the most recent surgical techniques, adjuvant medicines, and supportive care measures.

What Are the Advantages of Wilms Tumor Surgery?

The following are some benefits of Wilms tumor surgery for the treatment of this pediatric cancer:

  • Total Tumor Resection: The goal of surgery is to remove the Wilms tumor completely, which is essential for long-term survival. Surgery lowers the tumor burden and lowers the chance of spread or recurrence of the tumor by removing the main tumor mass.

  • Renal Function Preservation: When operating on a Wilms tumor, maintaining renal function is crucial, particularly when the tumor only affects one kidney (a unilateral Wilms tumor). Surgeons work to ensure total tumor excision while preserving the greatest amount of healthy kidney tissue. Procedures like partial nephrectomy and nephron-sparing surgery minimize the need for long-term dialysis.

  • Symptom Relief: Wilms tumor surgery can relieve symptoms like palpable abdominal lumps, hematuria (blood in the urine), and abdominal pain that are linked to the tumor. Surgery can enhance the patient's quality of life and relieve pain brought on by the tumor's growth and compression of surrounding structures by eliminating the tumor mass.

  • Facilitation of Adjuvant Therapy: Surgically removing the original tumor makes it easier to administer adjuvant treatments like radiation and chemotherapy. Surgery improves the effectiveness of these supplementary therapy methods by lowering the tumor burden, which lowers the risk of disease recurrence and improves outcomes.

  • Diagnostic Confirmation: Histopathological confirmation of the diagnosis is obtained through surgical biopsy or tumor removal in situations where the diagnosis of Wilms tumor is unclear.

Conclusion:

In summary, a key element of the multidisciplinary strategy for treating this common childhood cancer is the surgical removal of Wilms tumors. Over the years, there has been a major evolution in surgical procedures, driven by the goals of full tumor excision, preservation of renal function, and reduction of long-term consequences.

A new era of surgical accuracy has been brought about by the development of nephron-sparing techniques and minimally invasive operations, improving patient outcomes and increasing the quality of life for younger patients.

But problems still exist. Thus, the field has to continue researching and innovating. To fully address the complexity of Wilms tumor therapy, despite the impressive advances, there is still a need for additional improvement of surgical procedures, optimization of perioperative care, and investigation of innovative therapeutic modalities.

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Dr. A.K. Tiwari
Dr. A.K. Tiwari

plastic surgery-reconstructive and cosmetic surgery

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