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Category Archives: Birth Defects/Urinary Tract Abnormalities
Hi, My daughter postnatally was picked up to have dilated kidneys (both) She had surgery on both of these at 6 months and then 12 months (JJ Stints) the right one has been successful with it now looking normal. The left one is now stretched and still shows signs of dilation. She is 7 years old the right one measures 9.46cm and the left is 11.24cm. She has recently had an MRI and this showed the right one draining ideally the left one did drain however it was slower. The consultant has advised that we will follow up in 6 months with another scan as the left one may just be bigger and it might just be the way it looks now. My question is, with your experience would you have expected the left one to stabilise by now? They gave her a medication to reduce the time of the scan however would this have adjusted the results? (It took an additional 5 minutes for the larger kidney to drain under the medication so does this mean without it, is the urine sitting then and not draining or it does drain just a lot slower? If so is this of concern) Any advice on the long term management to avoid future problems would be appreciated. We have all images available and notes if required.
The problem that you describe is a urological problem. I am a nephrologist and have no surgical experience with childhood obstructive kidney disease. This problem is best handled by a urologist and not a nephrologist. I suggest that you continue … Continue reading →
Hello, My 9 year old son recently had an renal ultrasound to look for kidney stones, etc. We don’t follow up with the nephrologist for over a month, and I’m curious about ultrasound report. The nurse told me on the phone that he didn’t have kidney stones, and this is what the report actually says: 1. Mild right pelviectasis in the prone position only (7 mm). 2. Otherwise normal sonographic appearance of the kidneys. No definite calcifications are seen. In the prone position only, there is mild right pelviectasis (SFU grade 1 bordering on 2) with AP diameter of the pelvis measuring 7 mm. I assume the pelviectasis isn’t serious since the nurse didn’t bring it up on the phone, but never having heard the term before, I tried to research it. The only references I can find refer to fetal pelviectasis, and I can’t find anything about this condition in a 9 year old child. I’m also curious about it only being seen in the prone position. Does this point to the possibility of some sort of blockage, or is it likely just a physiological finding? Is it unusual in a child his age?
Pelviectasis (also called pelvocaliectasis) merely means a separation of the collecting system or pelvis of the kidney detected by the ultrasound device. It does not suggest any disease, unless there are symptoms or signs of blockage and none are described. … Continue reading →
For the past year, my 9 year old daughter has been getting regular immoglobulin treatments (Gammumex)which are responsible for a miraculous improvement in her mobility, since she has Chronic Inflammatory Demyelating Polyneuropathy. For almost a year she got the treatments at 2 week intervals and more recently at three week intervals. These IVIG treatments, necessary as they are, are hard on the liver and kidneys, but do you know just how toxic these IVIG treatments can be to a child’s kidneys over time? Have you heard of this type of treatment ever damaging the kidneys? She doesn’t get an especially high dose, just average, and her neurologist says any irregular reading on the kidney and liver test we took should be disregarded because that’s just due to the IVIG’s. But because this is a rare disease, most of the frequency/dose of the treatment still involves guesswork and experimentation, so I remain watchful for signs of stress on her body. In the last several months she is getting bladder infections now and then that she didn’t get before. So far they just go away with cranberry juice. Then in the last 6-7 weeks I usually have to push her to eat because she frequently gets stomach pain. She was never a big eater to begin with so I worry about her getting enough protein and losing alot of weight again, which she did when she was initially misdiagnosed, wasn’t getting these treatments, and lost most of her mobility. What scares me most is that I read everywhere about how there are no symptoms of kidney disease until it’s advanced. So should I be proactive/concerned, then? If you say yes, my next step would be to show the readings we have to pediatric kidney doctor in our hospital system, to see if a more detailed kidney/liver test should be taken The test the neurologist ordered wasn’t, I was told, but that’s because her neurologist is unconcerned. The reason I feel the need to check with a third party at times is because he was the one who misdiagnosed her, so I had to go to another doctor and then go back and convince him to give her these IVIG treatments, which I think saved her life.
I would recommend blood and urine testing for kidney disease at least every three months to monitor kidney function. This should include a serum creatinine and an estimated glomerular filtration rate (eGFR). Urine testing should be for blood, protein and … Continue reading →
I just read an old report of a blood test. The Doctor never said anything to me, but I had high protein in my urine and a few other things. They wrote possible kidney renal problems. This was taken at 52, I’m now going to be 54. I have had alot of bladder infections and one with my blood when i was younger. I had a scope of my bladder and I see a urologist for infections due to intercourse. They once said I had blood coming from my kidneys. No followup. I take prescription for infections when needed. I also don’t urinate all day then when I lay down I urinate alot. I do have marks on my legs from my socks and impression of fingers of swelling when you press on my legs. Should I be concerned? Get more tests? Sugar is good, actually I have low blood pressure.
I suggest that you have a urine test for blood, protein and infection sometime when an infection is not present and you should also have blood testing for creatinine testing and estimating your glomerular filtration rate (eGFR). These tests will … Continue reading →
My 9 year old son has had a very bright white, chalk-like residue in his underwear for several months. It is usually dried when I find it, and when I flake it off, it becomes powdery. It is definitely not a “discharge” from infection or seminal fluid. When I first saw it I thought it was paint, or white-out. When I examined it my first thought was that it looked like calcium (Tums) or some sort of mineral. He has had this once every week or so for 4-5 months, and I am now noticing that on days when he has it he often has an episode of stomach pain, which he describes as hurting fairly badly. He has never before complained of stomach pain so this made me pay attention and I noticed the correlation. It has not been accompanied by any pain or burning with urination until just the other day. That day he called me in to the bathroom to see a white, wet but powdery discharge, almost like wet chalk clumps. It was on his penis as well, and that time he said the opening in his penis hurt when he urinated. I was able to scrape a bit of the substance, which is like a hard flake, though very small. His doctor is having me take it to the lab to be tested. I’m curious if you’ve every heard of something like this, and what it might indicate? He is not dehydrated, and his urine is almost always a light straw color. Incidentally, the last week or so he has been waking with mildly to moderately puffy eyes.
I am unable to provide a specific diagnosis based on the information that you describe. This is a finding that I have never seen before. I suggest that you continue to work with your pediatrician and seek consultation based on … Continue reading →
Hello doc! My daughter is one and a half month old. She is having hydronephrosis plus hydroureter. The neurologist has recommended a test in which a tube will be passed inside her to check the actual problem. She is passing normal urine. An ultrasound concluded that the left side kidney is having a wrong replacement of its tube which connects the kidney with the bladder. That tube is going in the wrong direction. My question “Is this test safe for a one month old baby?
I am an adult nephrologist and do not see children or infants. I suggest you consult with a pediatrician or a pediatric urologist. For more information on Children’s health click here:
My baby was born two months early. Something happened in the NICU and she has lost her right kidney. She only has one now. She is now 10 months old. I am looking for any resources on how to keep her one kidney healthy. I am wanting to start her on good eating and drinking habits now. Do you recommend any books or people to talk to to keep her on a healthy track?
Many people live normal lives with a single kidney. I do not recommend any special diet. I recommend regular follow up with your pediatrician and regular testing of her kidney function with both blood and urine testing. No other special … Continue reading →
Can a male living in his 30’s live a long life on one functioning kidney without dialysis and kidney transplant?
Yes, many people live long and normal lives with one functioning kidney. I recommend that you have annual testing for blood and urine to measure the function of your single kidney. Your physician should dose any medications based on your … Continue reading →
Hi, I’m 34, female and have SLE (lupus) for about 16 years. Currently the protein in my urine is 2.82 and the doctor has put me on 500mg MYCOPHENOLATE MOFETIL (MMF), but I usually take it for a month and then my white blood cell drops below 4.That’s always the problem when treating my protein in urine. I think this is currently the only major problem preventing me from becoming pregnant, because my husband and I want to start a family, but the doctor told me it’s not the right time because of the protein in my urine. Is there something else I can do besides using my meds.
Systemic lupus erythematosis (Lupus or SLE)is a very dangerous disease for the kidney and also for pregnancy. This is a very complicated disease that can cause injury to your kidney, injury to you and injury to a developing fetus. Hence, … Continue reading →
My baby has a right ectopic kidney which is not working after we did DMSA scan last week. She is 3.7 years old. Due to frequent UTIs she has been getting since last year, her pediatrician sent us for further tests which then helped us to realize she had the ectopic kidney. 1. The physician advised us to monitor her for a year and if she gets more than 3 UTIs, then she should have the kidney removed. 2. While we wait, what can we do to ensure she avoids getting these UTIs? 3. What foods should we give her to ensure the left kidney continues working well ?
I am an adult nephrologist and have no expertise with children. I am not aware of any diet that would help this situation. I would recommend consultation with a pediatric urologist as the most appropriate physician to deal with this … Continue reading →