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Upper urinary tract anomalies and perinatal renal tumors
1Department of Urology, New York University School of Medicine, 150 32nd Street, 2nd Floor, New York, NY 10017, USA.
Insights
Congenital anomalies of the upper urinary tract are common and usually asymptomatic. Perinatal renal tumors are rare but treatable, with most infants cured after surgery.
Area of Science:
- Pediatric Urology
- Prenatal Diagnosis
- Pediatric Oncology
Background:
- Congenital anomalies of the upper urinary tract are frequently detected via prenatal ultrasound.
- These anomalies often remain asymptomatic unless infection occurs.
- Perinatal renal tumors, though rare, present a significant diagnostic and management challenge.
Purpose of the Study:
- To review the key features and long-term implications of congenital upper urinary tract anomalies for family discussions.
- To provide an update on common perinatal renal tumors and their treatment.
- To present a brief overview of normal renal development to contextualize congenital renal malformations.
Main Methods:
- Review of congenital upper urinary tract anomalies and their long-term outcomes.
- Update on the diagnosis and treatment of common perinatal renal tumors.
- Summary of normal renal embryogenesis.
Main Results:
- Congenital anomalies of the upper urinary tract are common and often asymptomatic, requiring careful discussion of implications.
- Most infants with perinatal renal tumors achieve a cure after primary surgical resection, often without needing adjuvant therapies.
- Understanding normal renal development aids in recognizing and managing congenital renal malformations.
Conclusions:
- Prenatal diagnosis of upper urinary tract anomalies facilitates informed family counseling.
- Early surgical intervention for perinatal renal tumors offers a high cure rate in infants.
- A foundational understanding of renal development is crucial for managing congenital renal conditions.
Abstract:
Congenital anomalies of the upper urinary tract are common and frequently diagnosed on prenatal ultrasound. In the absence of infection, these anomalies are often asymptomatic. This article reviews key features and long-term implications to assist in discussions with families. In contrast, a perinatal renal tumor is rare but extremely alarming. This update on the most common tumors and their treatment is useful in reassuring parents that most infants, after primary surgical resection, are cured without adjuvant therapies. To understand renal agenesis and other congenital renal malformations and their associated anomalies, a brief review of normal renal development is presented.
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