Recently there are red blood cells in my urine every time my doctor tests it and my ultrasound showed that my right kidney had mild hydronephrosis. My doctor order me to have a CT scan (IVP protocol). I don't know if MRI scan is more efficient than CT.
View 1 RepliesMy 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?
My husband was having flank pain so we went 2 doctor and did ultrasound.It revealed that he is having stone of 8mm in his left kidney and mid hydronephrosis in his right kidney.last year he had laser therapy for his kidney stone and 9months back when he did his ultrasound the stone was 6mm in size.and also he has a family history of kidney stone.Is it dangerous to have mild hydronephrosis or is it because of his stones.So once this kidney stone problem is finished will hydronephrosis automatically vanishes..?? or do he need 2 be treated for hydronephrosis..?
View 2 RepliesI am 54 year old female . I have had a trace of blood in my urine specimens at my yearly female checkups for the last 4 years. This year my dr. sent me to urologist.I am scared to death that if it is cancer, I've had it for this long.Anybody else had this symptom for 4 years and should I be worried?
View 2 RepliesI am a 27 year old female who has been on oral contraceptives for 7 years. I've never smoked and don't take any other medications. As part of a physical in June, my dr found microscopic blood in my urine. They did several retests and kept finding it. I had an ultrasound, cystoscopy, and CT scan. All were normal. My blood pressure has always been perfect. I have been referred to a urologist and they took a lot of blood without really explaining what they are looking for. Can you provide me with some insight? The dr did say she noticed a very small amount of protein but not enough to really bother her. This process has taken months and I never know how worried I am supposed to be.
View 1 RepliesI'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?
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?
Please guide me with available informations for Hematuria having dysmorphic red cells ,pain,left side face numbness.
View 1 RepliesI wonder if anyone has any info on "AAA".. during a routine physical checkup 2 months ago I had an ultrasound to follow up on "fatty liver" that was noted on a previous ultrasound 3 years ago. Well; I still have fatty liver and in addition they found a "mild" aortic aneurysm, fortunately found while still small. 3.2 cm diameter and 2.0 cm length, and also noted a 3.0 cyst upper pole of the right kidney, all other organs appear normal. The only advice I was given was to monitor with an ultrasound every year to make sure it's not growing. Dr. did not seemed concerned with the cyst on the kidney. Well; of course I am concerned !! I live in Honduras and plan on traveling to the Cleveland Clinic in Florida in October for a complete evaluation. That will be 6 months since the initial diagnosis. In the meantime; has anyone experienced something similar? do these AAA's tend to grow? has anyone had a cyst on the kidney do they tend to become malignant? I sure would appreciate anyone with any knowledge of these 2 conditions because I am "clueless".
View 7 RepliesRECENT HISTORY
First, I am diabetic and have had a fairly normal healthy life except in the last two years where I gained 40 pounds, did not control my blood sugars well, and went off the rails. I have had a lot of issues this year, but to focus on my most recent issues, I had a A1c of 10.5 two month ago and went to 9.1 a month ago finally to 7.6 right before my single incision laparoscopic with robotic-assisted single-incision surgery to remove my infected gallbladder (Hida Scan 11% no gallstones). 6 month ago i started experiencing a lot of bloating, indigestion and took charcocaps that helped a lot after meals.
Two weeks ago I went out for a cup of iced coffee (huge coffee drinker 3-4 cups a day for a long time no problems for years), and something hit me, it felt like a sharp pain and instant feeling of bleh no appetite and sick feeling the rest of the day. This continued for a week before I knew something was wrong, I could not have anything acidic or felt like I could eat anything. I had just seen my doctor for a bike accident a month prior to get a referral to a PT and osteopathic doctor. I had a l3/l4 compressed nerve with a twisted sacral (this is much better now with some minor spasms in my right leg from time to time). With all of that pain (took hydrocodone and muscle relaxants to sleep, sleep was poor) and school, I figured I must have given myself an Ulcer. My doctor game me a ppi-omeprazole (i've never had reflux and didn't then) since I had symptoms of some burning sensations and this chronic dyspepsia so this would treat the possible Ulcer for two weeks while I was sent for an ultrasound to check out my gallbladder (family history - Mom, aunt, and uncle had their's out with gallstones). The ppi sort of helped but I just was fatigued, could not eat anything but a bland diet, I had chronic dyspepsia and general nausea that I could never shake. My daily caloric intake decreased with each new day and food just made me generally feel sick, however if I skipped meals it would still be bad, worse with food.
TEST RESULTS
After the Hida scan came back positive with an ejection rate of 11%, I scheduled my new a1c test, ekg (family history of heart disease), I was cleared and scheduled for surgery. I stopped taking the ppi as I believed this to be the cause of all my problems. btw, I was 254 the end of june and lost 25 pounds by the time of surgery (average daily caloric intake ~900-1200 prior to surgery
POST SURGERY
After the surgery 7/21-one week ago, I had my two days of pain and adjustment, and recovered decently with a soft food and liquid diet. I noticed the general sickness was gone! Hazzah!, except on Saturday I was feeling bloated, cramping, and I could not eat a solid one bite without feeling sick. I knew I was constipated. I stopped the pain meds the day before and I knew I had not eaten too much but it was over a week since i went. I took magnesium citrate and nothing after 7 hours, I drank another 1/2--then BOOM it was insane. I was sooo wiped out and tried to replace lost liquids but I believe I was dehydrated. I was sick that night and stomach was not happy.
Sunday was much better but I was wiped out still and felt generally just depleted of all my energy. I ate, walked a bit and then came back home. That night I started feeling very uncomfortable and the symptoms were somewhat similar to prior to surgery of the general dyspepsia and nausea chronically. I could not sleep because of my back problems (had to sleep upright on my back all week). I woke up in the middle of the night turned to my side and then all of a sudden I felt a warm rush of something just above my stomach and the constant burn in my stomach no reflux. I could not sleep until the morning.
NOW,
I have had really bad gas (low fat diet) for the past few days. I was getting and feeling better on day four but now this!
I felt extreme discomfort all day, felt like a low grade fever 98.6 (no fever) incision site is also slightly red, but the doctor said to call if I had a fever. I was worried about an SSI. The pain was like I threw up (I never have even starting out back in at the coffee shop) and that ache afterwards. The burning sensation let up later in the day after I took some antacids and saltines (I must have some acid issues, but I have read a lot of people suspecting many people may actually have low acid).
The thing is a lot of people have episodes after food, but mine is chronic with mild discomfort, burning sensations, upper abdomen and stomach discomfort (with some nausea), and food helps it initially and then it comes back. I feel week, slight low grade fever even though I don't have one. I keep thinking I have an infection of H. Pylori or something. Food takes a while to do much, I walk after I eat everything. I feel like I could eat but I get so much bloating and indigestion that it is uncomfortable. I drink plenty of water, but I wonder if I am low on essential things for the long ongoing low calorie daily diet. I can't eat more then 800 calories even with smaller meals-since Thursday.
Why was my gall bladder inflamed in the first place? I had no stones, and the surgeon said I had a very long a big gallbladder (ready to rupture!) that was really inflamed including a little on the liver. Pathology reports came back negative. I theorize my rapid change in weight and blood sugar levels inflamed the organ or an infection.
Possibilities:
diabetic Gastroparesis
H. Pylori
Peptic Ulcer (was never officially tested)
Gastritis
Anxiety
Low/High Stomach Acid
Low bile leak?
Sphincter of oddi dysfunction
What I feel could help:
HCL Betaine
Digestive Enzyme (Garden of life chewable vegetarian)
ppi (I would hate to take them unless I had to)
something to coat my stomach if I do have an ulcer to heal
ability to eat more so I can have more assimilated minerals, ect.
Anxiety med (first year i've had a lot of anxiety-mainly school related and upcoming wedding planning for next year
more tests!
My burning anxiety questions:
When will I get my appetite back?
(i really suspected my odds were decently good that I would get better after surgery, I had a great surgeon)
Did anyone have any of these chronic symptoms? Is it due to an infection or some issue with surgery?
Have some people eventually been able to eat what they wanted after a period of time?
How many had these excessive bloating, indigestion, nausea and general malaise through the day, worse a little while after food or between meals?
I have a VERY mild soreness (if I can even call it that) just below my rib cage towards the right side, but only if I move in a certain way--it doesn't really hurt to the touch. I have no diarrhea, no fever, no back pain, stools are normal color---only a brief pang of nausea now and again, but it's not constant. Also, it doesn't bother when I eat greasy or fatty foods. I find it hard to believe that it's gallbladder related, but not sure whether I should see a doctor or not. It has subsided since the beginning of the week. Anyone else have this and it not turn into anything serious?
View 3 Replieshi 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?
View 1 RepliesI 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.
About a month ago, a random health check at work detected a slight trace of blood in my urine sample, by a dipstick. I went to my doctors a week later to check again and he found it. He ordered 5 different blood tests, sent my urine of to be checked and ordered an ultrasound. He said that if all was fine, then not to worry and its one of those things. All came back fine, even my urine was negative for blood which i did not understand. The doctor said that dipsticks are over sensitive and that the lab found nothing of any relevence. When i went back to a different doctor for scan resuts, which were clear, they did another dipstick which again showed traces of blood. Anyway, now i have been referred to a urologist and I don't know why. I am so worried that it might be cancer. But according the lab, i dont have microhematuria? I have no other symptoms at all.
View 3 RepliesI'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?
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.
Is it me or is this stuff a waste of time?
I've had obout 20 lithotripsy's in 15 years of having continuous stones. They've never gotten my kidney completely empty of stones ever. I've had lithos, ureterscopy, PCNL. On meds but they can't seem to stop them from growing. I avoid alot of the things that cause stones or limit them. Got to have the 1 cup of coffee in the morning
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.
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.
View 5 RepliesHello I am 19 years old I have been suffering with bladder and kidney infections since I was 14. I was admitted to hospital to find out what was wrong with me nothing could be found, I think I have tried every antibiotic under sun...nothing seems to help, I suffer with them every few mounts or so on and off.
When I fall ill with one I'm very ill it puts in bed for days with terrible pain and fever, I'm young and starting university very soon...I don't know anyone who suffers as bad as me and I struggle to get to the doctors a lot with being a full time student, it's so unbearable and frustrating can anyone help?.
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.
My doc did a urine culture last week, got results today and there was no protein in my urine, but I had 3+ ketones and a large amount of leukocytes. Blood work from a month ago just came in and my kidney numbers were off a month ago: BUN (32), Creatinine (1.8), eGFR (33). Between the symptoms and the blood test I'm thinking it sounds like renal failure, but could it be CKD without protein in the urine?
I am French. I’m 28, it’s being 2 years and a half that I have blood in the urine with horrible pain.
I had 3 ureteroscopies who have given nothing and now the professor who follows me told me I have the loin pain hematuria syndrome, and there was nothing to do. The only thing I can do is to wait till it’s going better. He refuses to make a biopsy and told me to take aspirin.
I wanted to know if you know doctors who offer other drugs. I've heard of self transplantation and kidney innervation;
I've been in different hospitals and doctors tell me that the pain is bearable and advised me to consult a shrink. I do not think my pain is psychic. I wanted to know if U.S. medical research is more advanced than the French one.