4th Pediatric Infectious Diseases Conference
 
 
Home  Back   ISSN 0973 - 0958
 
User name :
Password :
Pedi Poll
Today's Poll
Should teicoplannin, colistin be used in case of neonatal sepsis where culture does not reveal any organism_?
No, it should be used only after drug sensitivity report
Yes, under guidance of an infectious disease expert
WILM'S TUMOR (NEPHROBLASTOMA)
Wilm's Tumor (Nephroblastoma)
Dr Ira Shah
M.D, DCH(Gold Medalist), FCPS, DNB
Edited by Dr. Bharat R Agarwal
Consultant Pediatric Hematologist and Oncologist.


Q: How is Wilm's tumor staged?

A: The National Wilm's tumor study group has given a clinicopathologic staging system. The pediatric surgeon determines the clinical stage in the operation theatre and pathological staging is confirmed by the pathologist.

    Stage-I Tumor is limited to the kidney and is completely excised. It is seen in 43% of patients.

    Stage-II Tumor extends beyond the kidney through the perirenal capsule and is incompletely excised. It is seen in 23 % of the patients.

    Stage III Residual tumor confined to the abdomen. No hematogenous involvement. It is seen in 23 % of the patients.

    Stage IV Hematogenous metastases to lung, liver, bone, brain, or combination of these sites. It is seen in 10 % of the patients.

    Stage V Bilateral renal involvement at the time of initial diagnosis. It is seen in 5 % of the patients. Each site should be staged according to the above criteria on the basis of the extent of the tumor prior to biopsy.
Q: Why is it necessary to have a histopathological examination in Wilm's tumor?

A: Although most patients with a histopathological diagnosis of Wilm's tumor do well with treatment, there are 2 categories of unfavorable histology -

  1. Anaplasia

  2. Sarcomatous changes (includes clear cell sarcoma of the kidney and malignant rhabdoid tumor of the kidney.)
Q: What are the prognostic factors?

A: Though Wilm's tumor is curable in almost 90 % of the patients, the prognosis is related to the stage of the disease at diagnosis, the histologic features, age of the patients and the tumor size.

Q: How is Wilms' tumor treated?

Treatment of Wilm's tumor consists of a combination of surgery (nephrectomy) followed by chemotherapy and in some patients, radiation therapy. It all depends on the histology and stage of the disease.

National Wilm's Tumor Study IV Recommendations are:

  1. Stage I -Favorable history or anaplastic

    Nephrectomy + Chemotherapy (vincristine + Actinomycin D)
    x 6 months
    No Radiotherapy

  2. Stage II -Favorable histology

    Nephrectomy + chemotherapy (vincristine + Actinomycin D)
    x 15 months
    No Radiotherapy.

  3. Stage II (Anaplastic),III & IV

    Nephrectomy + Radiotherapy + chemotherapy (vincristine + Actinomycin D + Adriamycin) x 15 months

  4. Clear cell sarcoma (stage I to V)

    Nephrectomy + Radiotherapy + chemotherapy (vincristine + Actinomycin D + Adriamycin) x 15 months
Q: How are patients with Wilm's tumor followed up?

As stated earlier, abdominal ultrasound is done once in 6 months for two years and then yearly for an additional 1 to 3 years. Chest X ray should also be repeated at the same time. The patient with pulmonary disease at diagnosis should have a repeat CT scan every 3-6 monthly for 2 years and then yearly for 1-3 years.

Last created on 13-07-2001
Last updated on 01-07-2006

 
 
Educational Section
 
Disclaimer:
The information given by www.pediatriconcall.com is provided by medical and paramedical & Health providers voluntarily for display & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk. The appearance of advertisement or product information in the various section in the website does not constitute an endorsement or approval by Pediatric Oncall of the quality or value of the said product or of claims made by its manufacturer.
 
copyright ©2011 website design & development by Levioza
Follow Us
Follow us on :
Folllow Us