urine test results lupus nephritis

I, like you, cannot understand why your doctor will not test for Lupus Nephritis. You do think this would be the next step here :( x This said, have you been checked for vesicoureteral reflux. My daughter has this (along with a duplex kidney system). This causes urine to flow back up the ureters and kidneys. voiding cystourethrogram (VCUG) is commonly used to diagnose this. If this is happening it causes repeat UTI's and gives pain as you describe.

Hi, One of the goodies which comes along for some of us Lupus patients is Lupus Nephritis. Some of us are also on certain meds which cause kidney damage or deficiancy not related to Lupus Nephritis. Right now your kidneys are OK. Repeating it in three months maybe because you are on cerain meds or in the process of you being tested for Lupus your doctor would like to keep a close watch on your kidneys particularly if you are having what is known as a Lupus Flare.

According to your test result, you may have inchoate nephritis, the remarkable urine protein and urine blood is inchoate nephritis’ important characteristic, but it cannot be diagnosed by the result of only one time of urine test, you can do urine test twice another week, and tell me about your test result, so that I can help you to get diagnosis

After a biopsy I was diagnosed with interstitial nephritis. I was wondering if anyone has heard of this? Does it ever go away? I have large amounts of blood and protein in my urine and my kidney functions are decreased and have been for about 4 years already. I am scheduled with a kidney dr in a few weeks. Because it has been a year I am getting a little concerned. My DR doesn't have a lot of answers for me.

sDNA is highly diagnostic of systemic lupus erythematosus (SLE) and implicated in the pathogenesis of lupus nephritis (inflammation of the kidney caused by SLE). High calcium can be seen with SLE due to either the immune system targeting the parathyroid glands (extremely rare) or more commonly due to kidney problems.

recently diagnosed of sle with lupus nephritis type v and is currently on omnacortil(prednisolone) 40mg/day and chloroquine at 24 yrs of age now ive started to notice my moon like face after 2 weeks and its getting wierd and wierd.is there any way to be out of my new face ...

I wont be seen till July 8th and that was the earliest out of several doctors called. I need blood work and a 24 urine test (I have Lupus Nephritis as well) One more thing. This past weekend I forced myself to attend the Lupus Foundation Symposium (Greater Washington Chapter) In spite of my pain I am sooo glad I went. It was very insightful.

I am not thirsty but I have to drink water to keep up with my unrinating or I will get dehydrated. I went to the doctor and he did a urine test and blood test to make sure it wasn't diabetes or kidney problems and the tests came back with no problems at all. My lower back hurts as well but the doctor says its probably not related. It has me worried and annoyed. Is it possible that I have a pinched nerve thats making me produce more urine? Any suggestions or ideas?

s nothing major at the moment, but you do need to have it monitored, because anything over 0.3g per 24 hour urine collection is significant. And if you do have nephritis, you will need to be on medication. Is your kidney function normal? I guess it should be. Any RBC or WBC in your urinalysis? Normal blood pressure?

Thanks for the feedback. I do have lupus nephritis, and have had this disease for 3 years now. Do you think it's the lupus that's triggering this numbness in my right side. And also the doctor told me that it couldn't be my lupus. I'm just concern and need to know the next steps that i should take when i go see my doctor and also i will get a second opinion.

Complement 4 or C-4 is a protein that moves freely in blood and helps in inflammation. Usually this test is done to monitor response to management of autoimmune disease. C4 and other complements are low in lupus and high in rheumatoid arthritis and certain cancers. Decreased component activity is also seen in nephritis, cirrhosis, bacterial infections, malnutrition, hereditary angioedema, and hepatitis. Hope this helps. Do let me know if there is any thing else and keep me posted. Take care!

I disclosed all preexisting medical issues before my colonoscopy , chronic kidney stones since the age of 6 and I am 40 now. Extreme urinary issues and lupus nephritis and so much more. So on March 23rd I had my colonoscopy ( narcolepsy and that jug they make you drink is no fun , had to was my p.j. pants twice and change my bedding threw the night ) anyways I awoke having to pee like a race horse.

I have been doing researches on the recipe,which handed down from my forefathers,can cure all kinds of nephritis(except Kidney Failure and Uremia because they are not reversible). The recipe is comprised of several kinds of plants and this (secret) recipe has never become published.I assure you that the mixture contains no toxic substance.This prescription is characteristic by miraculous curative effort and short course of physiotherapy (according to the state of illness).

Sorry I'm late chiming in Lisa. Parts of my LP testing were also done at Labcorp facilities in Dublin OH and Burlington NC. The report specifically reported "Oligoclonal Banding testing was performed using Isoelectric Focusing (IEF) and immunoblotting methodology". At least you can put that question to rest. You can certainly thank the doc that gave you "all" the results on the 14th (make sure you hear the sarcastic tone there).

I got my test results back today for hbsag quant. I cant believe we finally have the test in the USA. I am 38 years old hbega - , dna under , genotype c, percore and core mutations. my hbsag quant came out to 1100 , which made me very surprised. Do you think I am a good candidate for interferon. Kidneys are not the greatest at 1.3 and i have been on entecavir for 18 months now. Can i get some opinions from previous interferon patients and also wondering about decline of hbsag after treatment.

t favor a Type II MPGN diagnosis because the prognosis is much more grim. After the results of this test, I guess the doctors will probably move forward with a biopsy. Is there anyone out there who has gone through this before? I am so emotionally overwhelmed with the waiting, and the lack of answers. Any help is appreciated. Thanks!

What were the results of your test? Was a random urine sample for protein levels done? What was the result regarding your glomerular filtration rate?

Urine test results lupus nephritis

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