Wilms' tumor
(Redirected from Wilms Tumor)
Contents
Background
- Affects children <15yr, 2/3 of cases diagnosed before age 5[1]
- Arises from persistent embryonal renal cells
- Most common renal malignancy in children[2]
- 10-15% will have mets at presentation (lungs)
- 10% of cases are associated with malformation syndromes such as WAGR, Denys-trash, Beckwith-Wiedemann[3]
Clinical Features
- Abdominal swelling/mass, can have abdominal pain
- Avoid vigorous palpation to prevent capsular rupture; causes tumor spillage (will then need more intensive therapy)
- Subcapsular hemorrhage presents as abdominal enlargement, anemia, HTN, and possibly fever
- Patient often appears well
- Less frequent features include abdominal pain, hematuria, fever, anorexia, nausea/vomiting, hypertension[4]
Differential Diagnosis
- Neuroblastoma
- Other renal cell tumors are rare in children
Evaluation
- Ultrasound, CT or MRI
- Chest imaging to look for lung mets, usually CT
- CBC, chemistry including serum calcium and creatinine, LFTs, coags
Management
- Consult oncology/surgery
- Surgery/biopsy, chemo, and/or radiation based on staging
Disposition
- Admission for further workup and management
References
- ↑ https://www.uptodate.com/contents/presentation-diagnosis-and-staging-of-wilms-tumor?search=wilms%20tumor%20children&source=search_result&selectedTitle=1~120&usage_type=default&display_rank=1
- ↑ https://www.uptodate.com/contents/presentation-diagnosis-and-staging-of-wilms-tumor?search=wilms%20tumor%20children&source=search_result&selectedTitle=1~120&usage_type=default&display_rank=1
- ↑ https://www.uptodate.com/contents/presentation-diagnosis-and-staging-of-wilms-tumor?search=wilms%20tumor%20children&source=search_result&selectedTitle=1~120&usage_type=default&display_rank=1
- ↑ https://www.merckmanuals.com/professional/pediatrics/pediatric-cancers/wilms-tumor