WILMS TUMOR
By Nuzul Alimi
Introduction
Wilms tumor, also known as nephroblastoma, is
a cancer of the kidneys that typically occurs
in children, rarely in adults.
Introduction
Wilms tumor is the most common childhood renal tumor,accounting for
approximately 6 % off all pediatric malignancies
This tumor tends to occur between ages 1 and 3 years
The incidence of wilms tumor is 1 in 10000 children
HISTOLOGY
EMBRIONAL RENAL
NEOPLASMA
BLASTEMAL
STROMAL
EPITHELIAL
CELLS
Histology
Wilms tumors may be separated into 2 prognostic
groups based on pathologic characteristics:
Favorable - Contains well developed components
mentioned above
Anaplastic - Contains diffuse anaplasia (poorly
developed cells)
Sign and symptoms
Typical signs and symptoms of Wilms tumor include the following:
a painless, palpable abdominal mass
loss of appetite
abdominal pain
Constipation
SOB
fever
nausea and vomiting
blood in the urine (in about 20% of cases)
high blood pressure in some cases (especially if synchronous or
metachronous bilateral kidney involvement)
Diagnosis
Chest radiography detect pulmonary metastatis
Abdominal radiography linear calcification
Ultrasound characteristic of the
mass,intravascular involment
Ct scan of abdomen
Biopsy(not typically performed due to seeding of
malignant tissue into abdomen) type of tumour
tissue.
Abd x ray
Diagnosis
Staging
Treatment
The main types of treatment are:
Surgery-nephrectomy
Remove the tumour.
Chemotherapy
radiation therapy
Prognosis :
The overall 5-year survival is estimated to be approximately
90%
In case of relapse of Wilms tumor, the 4-year survival rate for
children with a standard-risk has been estimated to be 80%