Fetal hydronephrosis
Hello Dr.
Chang,
I am currently 26 weeks pregnant.
During a self-paid high-resolution ultrasound check-up at the hospital the other day, I was shocked to discover that the left kidney of my baby is severely hydronephrotic (4.7 cm).
After evaluation by the doctor, it seems that the kidney function is almost zero, while the right kidney is structurally normal but also has mild hydronephrosis.
Could you please explain what might have caused this condition? Both my husband and I, as well as our families, are in good health.
What treatment options are available for the baby? Will the severe hydronephrosis on the left side compress other organs? If the delivery goes smoothly, what treatments will be necessary afterward? Is it possible that there is a genetic issue involved? However, the ultrasound indicated that other areas of the baby are normal.
What should we do at this point? Thank you.
Hao danxin de zhun mama, 20~29 year old female. Ask Date: 2005/05/20
Dr. Zhang Peixin reply Pediatrics
Hello: Hydronephrosis generally refers to the dilation of the renal pelvis, most commonly caused by a narrowing at the ureteropelvic junction.
However, there are other causes that can also lead to renal pelvis enlargement, such as severe vesicoureteral reflux and ureteral strictures.
Your baby was found to have a 4.7 cm hydronephrosis on the left side during the prenatal ultrasound, which is significantly larger than the normal kidney size for a 26-week fetus.
It is also possible that this is not hydronephrosis but rather a degenerative cystic kidney disease due to the absence of renal tissue development.
A definitive diagnosis can only be made after the baby is born and examined directly.
At this stage, whether it is hydronephrosis or an underdeveloped renal cyst, since it is unilateral, the other kidney is functioning normally.
Additionally, the position of the kidneys in the retroperitoneal space does not pose a significant concern for compression issues, and it will not compress the contralateral kidney.
Therefore, there is currently no need for treatment, and the mother should remain calm and prepare for delivery.
Based on your description, it does not seem to be an autosomal dominant or recessive hereditary polycystic kidney disease.
The aforementioned causes of hydronephrosis are often related to issues during embryonic development and are not uncommon, differing mainly in severity.
As for whether it is a genetic inheritance issue, there is currently no conclusion.
I recommend that you continue with regular prenatal check-ups and consider delivering at a hospital with pediatric nephrology and pediatric surgery services.
You may also want to consult with a pediatric nephrologist beforehand.
Within 1 to 3 days after birth, you can arrange for your baby to have a renal ultrasound and related examinations for vesicoureteral reflux to make an accurate diagnosis and plan appropriate treatment.
The principle is that if it is hydronephrosis, treatment will depend on the severity and renal function, which may include decompression, surgery, or monitoring.
If it is degenerative cystic kidney disease, then only monitoring is required without immediate intervention.
The pediatric nephrologist will provide a detailed explanation of the situation during the outpatient consultation.
Sincerely, Dr.
Zhang Pei-Hsin, Pediatrics.
Reply Date: 2005/05/20
More Info
Fetal hydronephrosis is a condition characterized by the swelling of a fetus's kidney due to a buildup of urine. It can occur when there is an obstruction in the urinary tract, preventing urine from draining properly from the kidney to the bladder. In your case, the left kidney is significantly affected, measuring 4.7 cm, while the right kidney shows mild hydronephrosis but is structurally normal.
Causes of Fetal Hydronephrosis
The causes of fetal hydronephrosis can vary and may include:
1. Obstruction: This is the most common cause and can occur at various points in the urinary tract, such as the ureteropelvic junction (where the kidney meets the ureter), the ureter itself, or the bladder outlet.
2. Vesicoureteral Reflux: This condition occurs when urine flows backward from the bladder into the ureters and kidneys, leading to swelling.
3. Genetic Factors: While you mentioned that both you and your husband are healthy, some cases of hydronephrosis can be associated with genetic syndromes or congenital anomalies.
4. Infections: Urinary tract infections can also contribute to hydronephrosis, although this is less common in utero.
5. Other Anomalies: Sometimes, hydronephrosis can be a part of a broader spectrum of congenital anomalies, which may not be immediately apparent on ultrasound.
Treatment and Management
The management of fetal hydronephrosis largely depends on the severity of the condition and the underlying cause. In your case, with the left kidney showing severe hydronephrosis and almost no function, close monitoring will be essential. Here are some steps that may be taken:
1. Monitoring: Regular ultrasounds will be necessary to monitor the size of the kidneys and assess any changes in function.
2. Postnatal Evaluation: After birth, the baby will likely undergo further imaging studies, such as a renal ultrasound or a voiding cystourethrogram (VCUG), to assess kidney function and check for any obstructions.
3. Surgical Intervention: If significant obstruction is found after birth, surgical intervention may be necessary to correct the issue. This could involve procedures to relieve the obstruction or to re-route urine flow.
4. Nephrology Consultation: A pediatric nephrologist may be involved in the care of your baby to provide specialized management of kidney function and any potential complications.
Concerns About Organ Compression
Severe hydronephrosis can potentially compress surrounding organs, which may lead to complications such as impaired lung development or gastrointestinal issues. However, the extent of these complications often depends on the severity and duration of the obstruction. Regular monitoring through ultrasound can help assess any impact on other organs.
Genetic Considerations
While genetic factors can play a role in congenital anomalies, the presence of hydronephrosis alone does not necessarily indicate a genetic problem, especially if other ultrasound findings are normal. However, if there are concerns about genetic syndromes, genetic counseling and testing may be recommended.
Next Steps
Given your situation, it is crucial to maintain open communication with your healthcare provider. They will guide you through the necessary monitoring and interventions. It is also advisable to prepare for a multidisciplinary approach postnatally, involving pediatricians, nephrologists, and possibly geneticists, to ensure comprehensive care for your baby.
In conclusion, while fetal hydronephrosis can be concerning, many cases are manageable with appropriate care and monitoring. Your healthcare team will be your best resource in navigating this situation and ensuring the best possible outcome for your child.
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