Kidney :: Microscopic Hematuria In 3 Yr Old Son
Aug 22, 2013
My son is of 3 years old.
Last month he was having fever so doctor suggested me to go through CBC blood test and urine test.
The CBC count was normal except the wbc count was more.
In Urine test it found color yellow, protein present+, puss cells 9-10 and rbc 7-8.
Again doctor treated with some antibiotics. With the help of those antibiotics there was no fever.
Again after a week we went under urine test the result was same.
Till now 4 time urinalysis has been so far and the results vary from sometimes RBC is between 2-3 to 7-8, Puss cells between 1-2 to 9-10 and protein from trace to present+.
So my doctor referred to a Nephrologists.
Nephrologists asked to go for Abdomen test and the results were normal. This was done last week.
Today again we went for urine test still the results are same Color yellow, protein present+, puss cells 9-10 and rbc 7-8.
My Nephrologists told me that there is no problem as the protein level is low.
He told me to regularly do urine test every 3 months and keep a track of protein level.
He also suggested me not to go for kidney biopsy as it is not needed now.
So what could be the reason behind it and what should I do?
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I'm posting here on behalf of my sister in law. She's 29 years and since 2 years she's in dialysis. We're looking at the option to perform a transplant.
Her mother is a potential donor and we did all the tests. Everything was fine except for Hematuria (that is Erythrocytes in urine). After the doctors reviewed the result they told us she can't donate. I feel that while she may not be the best donor, they didn't want to take any risk.
I wanted to ask if anyone did a transplant while the donor had Hematuria?
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For the last five months I have been experiencing blood and protein in my urine. After a very thorough assessment from a urologist everything came back normal. I was referred to see a nephrologist to see if the blood is coming from my kidneys. my kidney panel came back normal except for lower than normal creatinine levels???? but my urinalysis came back all wrong. It's showing 3+ for blood, 100 mg for protein, 1+ bilirubin, urine color is brown, ph of 5.5.
The dr also order a ANA test to check for lupus, but it came back negative. I'm completely lost, can a person have kidney disease w/normal kidney function?or lupus nephritis w/negative ANA test?
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Please guide me with available informations for Hematuria having dysmorphic red cells ,pain,left side face numbness.
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hi doc whenever i blow my nose i see tiny microscopic red hairs with mucus like 1 or 2. is this blood or fiber? i put peroxide on it to see if it would turn brown but it just stays bright red. what can it be?
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I found blood in urine yesterday (Saturday) So today I went to urgent care.
The following tests were performed:
"CBC With Differential"
"Comprehensive Metabolic Panel"
"Urinalysis With Microscopic"
"XR Abdomen AP."
Doctor said that everything appeared normal, but my GP may follow up with a CT scan. Why? I'm really scared about this, but I thought something really serious like a malignancy would show up in blood work.
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I've been avoiding going to the Dr's for a while now, as I'm very scared.
Every few months, I have a day or so where I urinate blood. Also some blood clots. No real pain.
Then it will seemingly disappears for a few months, and will then return for a day or so.
I'm assuming it's something terrible.
Other symptoms seem to be frequent/weak urination.
Sometimes a mild/dull pain in one of my testicles.
Has anyone experienced this? WHy would it be every few months like this?
I plan to call my GP tomorrow as it happened again a minute ago for the first time in a few months and i'm plucking up the courage.
I'm petrified of the cystoscopy. (pain and embarrassment)
I had my urine tested for an unrelated issue a while ago, and it was apparently 'clean' (even though this was only a day after i'd been urinating what looked like almost pure blood)
How can this be?
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I am a 17 year old female.
For about four months now I have been experiencing problems with fully emptying my bladder and had trouble with leakage, even wetting myself completely once.
I went to my GP who tested my urine with a dipstick and found traces of blood. My GP also sent off a urine sample to the lab but this has come back negative for blood which confused me.
I have been referred to a urologist and have been booked for a kidney and bladder ultrasound in a couple of weeks.
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Is it me or is this stuff a waste of time?
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On the day before litho, your suppose to eat light ( nothing that leaves residue in bowl) but they say you can have white bread or boiled chicken. (Why bother?) I usually only eat jello, gatorade, and just broth. Plus tons of water. The instructions say to drink the magnesium of citrate after dinner. Well to me dinner is after 6/7. But I thought this time I would take earlier since last time didn't start to move the bowels until i was in the hospital. Plus this stuff is awful- taste bad- even refrigeration like they suggest doesn't really help. Twice in past I threw it up.
So I took at 5 pm thinking it would work earlier. Nope. Nothing. Just stomach cramping and it finally started around 5 am after me getting up every hour during night. Still was working again while in hospital.
There has to be something better (tasting) and work faster. Plus less side effects. Or they should change instructions & say take a noon. Next litho (in 2-3 months) I'm taking a 1/2 day off day before and taking at noon. Maybe then can get a little sleep the night before procedure.
Sorry- felt like ranting as frustrated as its been two full days since litho and nothing passing yet. Plus I have a bad back (2 surgeries) which makes it hard to do the exercises where you drink 2 cups water, wait 30 minutes, then elevate kidney @ 45 degrees and stay like that for 30 minutes to try and get the pieces to move.
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I was just wondering if anyone has protein in their urine with Chronic Kidney Disease and what did your doctor do about it if anything. I am trying to keep my GFR stable. The last time it went up a bit but am worried about the protein causing more damage quicker.
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Is it possible to have CKD or kidney failure without protein in urine?
Last week my masseuse found a knot in my back that she suspects could be inflammation in my kidney. I've had some weird symptoms popping up over the last month like foot/ankle swelling, profound fatigue, leg cramps and blurry vision. This last week though I began developing SEVERE flank pain (like 9 on a 10 scale), back pain (started out lower, now entire back), horrible nausea, horrible headaches, shooting pains down my legs, metallic taste in mouth, dizziness and loss of appetite. Not to sound melodramatic but I feel like I'm dying. The pain is constant but the intensity seems to be moving in 24 hour cycles. Today I feel awful but I was able to shower/get dressed. Yesterday I couldn't even get out of bed. I slept for 16 hours. It's been going in that pattern for the last week and a half.
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In the last week of Jan I was diagnosed with a bad kidney infection and given a weeks antibiotics (can't remember the name). After 2 weeks feeling no better I went back to docs with a sample and the infection was still there and given 3 day course of antibiotics (naturfranton (not sure of spelling)) and was told to come back again the next week with a sample. This time the sample was clear but a week later I was back with flank pain and generally feeling unwell, there was no infection in urine but I was sent for blood tests to test my kidney function etc and sent for an ultrasound. All of these tests came back clear. 2 weeks later back again feeling unwell, nausea, pain around bladder, upset stomach and received 3 day course of trimethoprim. I finished this course and finally felt normal only ten days later to be back with nausea and kidney pain and I am currently on a 5 day course of amoxicillin.
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I have had a low GFR for a year now but recently it has went down to 51 and I'm passing urine a LOT more often and feel I've a pinching pain under my right rib. Does anyone have any suggestions?
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