HemeOnc
Nephroblastoma
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Nephroblastoma
, Wilms Tumor, Wilm Tumor, Kidney Adenomyosarcoma
See Also
Childhood Cancer
Neuroblastoma
Epidemiology
Age Peak
Incidence
: 2 to 5 years old
Earlier onset in familial type Nephroblastoma
Accounts for 5-7% of all
Pediatric Cancer
s
U.S.: 600 new cases per year
Most common renal
Cancer in Children
Pathophysiology
Embryo
nal pediatric tumor of the
Kidney
Mixture of cell types (blastemal, stromal, and epithelial)
Symptoms
Constitutional
Fever
Appetite loss
Weight loss
Malaise
Gastrointestinal
Abdominal Pain
Nausea
or
Vomiting
Constipation
Genitourinary
Hematuria
Scrotal Swelling
Miscellaneous
Anemia
Hypertension
Findings
Presentations
Incidental Abdominal Mass
May occur as sporadic, non-syndromic case (or as part of WAGR syndrome)
Firm unilateral mass below rib margin
May present with complications (e.g.
Small Bowel Obstruction
)
WAGR Syndrome
Wilms Tumor
Aniridia
Genital anomalies
Mental Retardation
Metastatic Disease
Present in 10-15% of Nephroblastoma cases at presentation
Metastases are most common to regional
Lymph Node
s, lung and liver
Imaging
Abdominal XRay
May demonstrate complications such as
Small Bowel Obstruction
Abdominal Ultrasound
May define
Renal Mass
, and demonstrate complications
CT Abdomen and Pelvis
with contrast (or MRI
Abdomen
and
Pelvis
)
Preferred study to characterize tumor, extent of involvement and complications (e.g.
Hemorrhage
)
Often obtained with CT chest with contrast in suspected Wilm Tumor (Consult oncology)
Management
Consult pediatric oncology
Typical transfer to tertiary center for multispecialty care
Small Bowel Obstruction
Consult pediatric surgery
Decompression of
Small Bowel Obstruction
(
Nasogastric Tube
suction, NPO)
References
Collyer, Huang and Seo (2026) Crit Dec Emerg Med 40(1): 26-33
Leslie (2023) Wilms Tumor, StatPearls
https://www.ncbi.nlm.nih.gov/books/NBK442004/
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