Arthritis :: Synovial Effusion But No Joint Damage ?
Dec 20, 2015
I am 22 years old. I have just read all the symptoms of Osteoarthritis and it matches to what i have been facing from 3 years. I have a consistent pain in my Right Hip joint it is felt when I move my leg. Im facing Limited range of motions in joint and my joint have also become weak i don't have strength in right leg to lift any weight with that joint.
I have been diagnosed with all possible lab blood tests including (T spot and TB gold test) , Xrays, Mri and Bone scan.
The report of MRI tell that there is some Synovial Effusion found in the joint and the open biopsy is recommended. Furthermore from X Rays and MRI its clear that there is no damage happened to the Hip Joint so far.
I want to get to know if there is no damage happens to Joint if its possible that its osteoartritis?
If no what could be possible disease I could have with the same Symtoms like ie limited range of motion of hip, Loss of strength in the leg, Pain when you move it.
Doctor thinks it could be tuberculosis but the blood tests (TB gold, T spot) to check TB are clear. Bone scan is clear. Lungs X rays are also clear.
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Hi Experts,
I have been into long distance running since long. Lately I started suffering from severe heel pain for which I had an MRI which says:
1. Minimal joint effusion is seen tibiotalar joint anterior and posterior recesses.
2. Soft tissue edema is seen in kager fat and anterior of ankle.
3. Minimal insignificant fluid in subtalar joint and intertarsal joints.
Its been two months I have not been running and I am feeling equal pain all the time. Pressing heel by thumb gives me worst pain. I can't move barefoot anymore. Orthotics insoles provide relief.
I have been dipping my legs in ice water and not running since 2 months but no relief at all.
I am 31 year old male, 5'11" and 78 kg.
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One of my great loves is walking. I love walking and love walking my dogs and not only that they expect a walk every day! However, I have along with all my spine issues (arthritis, stenosis), I also have three synovial cysts at the L3/4 level. I have a very consistent pattern, I start out the walk great, but by the end of the walk I am in such pain and with very painful spasms.
I am be followed by my pain management specialist who has been doing regular epidural injections, unfortunately there is so much scar tissue it is difficult to give me the injection on one side of the lumbar spine and I am finding the injections are lasting less and less time. The other problem I have is with my left knee and and am seeing an orthopedic specialist for this and just received a Synvisc injection. I am still dealing with a lot of pain in my knee - sometimes I feel like I am falling apart!
The problem I have is I know my basically my next steps would surgery for my spine to remove the cysts and surgery on my knee (not sure what procedure my orthopedic surgeon has in mind). Maybe, I'm just over thinking this - it is just awful to have multiple pain issues. I am just wondering how I would prioritize. At this time it would seem like the lumber spine is the priority, because sometimes I can't even roll over in bed without my husband helping. I am worried what I will like in 15 years - it is a scary thought. :sad: BTW - One thing both of my Doctors have suggested is a stationary bike and I understand that for exercise and it takes the pressure off the knee and spine, however I love getting out and walking with my dogs it is one of pleasures that I don't want to lose - even if I have to crawl home at the end of the walk.
Addition (Added 3/25/14) - Also, I am wondering if anyone has any suggestions to keep me walking - I understand my Doctor's viewpoint that other exercise options are easier on the spine (eg, stationary bike), however I just don't want to give up my daily walk. I am just wondering if there is anything that might help stop the spasms or reduce them.
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I have had moderate to severe joint pain since April, and was recently diagnosed with Parvovirus B19. Apparently the virus can cause severe Arthralgia that lasts upto 9 months.On good days my pain level is at a 3. On bad days it will go upto a 6/7. Yesterday I stepped on a metal wire and it got stuck in my foot. The urgent care center recommended I get a tetanus shot, since I have not had one in over 10 years. I asked what the side effects were, and they said my arm would be a little sore.
Well, " a little sore" does not quite describe it. My arm was in excruciating pain all night and still really bad today. I can't even lift it more that a couple inches. Also, all my joints on my left side ( side I got the shot) were in excruiating pain 8-9. I just sat in bed and cried last night. I took 3 tylenol arthritis's and an extra Meloxicam that I have for joint pain and it did nothing, My arthritis continues to be really bad today. I called the urgent care and asked if I could come back in to get some medication to work until the pain stops. They said they could not do that, and that the tetanus shot would not aggrivate arthritis.
Let me know if anyone else has experienced worsened arthritis symptoms after a vaccination or shot. I wanted to get the flu shot soon, but I am scared now. Can the Flu shot make me hurt this bad as well? Let me know If I should tell the doctor and ask for additional pain medication. Or if the doctor will just tell me " No".
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I have just read about a new procedure for surgery of the CMC joint in the thumb. It's a much smaller infusion, doesn't involve removal of a whole bone and is supposed to have a much faster recovery time and little loss of strength. It involves an implant called the Bio Pro thumb implant.
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I have a problem and need advice! My family is known to have history of arthritis. I am 34, male and I am afraid I have this disease too. I feel tingling in my temples. Is this a symptom of arthritis?
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Had knee replaced 2009. Last year developed cellulitis and septic arthritis one day prior to having other knee joint replaced.
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I had surgery on June 14, 2011 to remove a bone spur on my left clavicle and to remove arthritis near (but not in) my shoulder joint. It was the worse experience of my life. I was in constant agonizing pain for 2.5 months. Just for the record, I've had two ulnar nerve surgeries on my left AND right elbows and never even needed pain medication. This shoulder surgery apparently did not relieve any of my pain. I still have a dull aching pain through out the day starting in my neck (left side) to my shoulder, and down my bicep to my elbow. I still can not sleep at night, and through out the day while working my shoulder/arm/ neck is killing me. I continue to take an Naproxin and continue to rotate heat and ice. I did physical therapy for the first two months after surgery. My concern is that had arthroscopic surgery, and there was NO rotator damage so why is my shoulder still in pain? My shoulder pops when I do try to rotate it.. and often when I simply reach outward for something..I'm in excruciating pain. I'm a baker, so I am constantly lifting a 34-50lb metal mixing bowl and have to reach many times through out the day. There really is no way to not do my job duties and still retain my job. Any ideas why I'm still having this problem?
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I have had a viral chest infection for 10 weeks, have just gone back to work part time after 6 weeks off sick. My cough went weeks ago but I still feel unwell (which varies day to day) with lung pain (worse when I lie down, walk, bend etc) and ringing in the ears.
I am worried about how long it is taking to get better, the Doctor gave me nothing apart from painkillers and said it is just a nasty bug. I am also worried whether going back to work was the right thing, do you think it will make it worse?
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I have had ongoing pain for the past 2 months, worse when breathing in on the right side of my chest. My doctor has diagnosed pleurisy and said it should resolve on its own. I have now developed a very sore collarbone on the opposite (left) side. Could these two symptoms be related? I have health anxiety and am convinced I have terminal breast cancer....silly I know!
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After MRI my diagnosis was "Lots of mileage left, another 10 years, at least!" (I am 75)! Good to hear but still have to be careful going DOWN stairs! Not too bad going up! Some pain now and again. BUT I sometimes get a strange feeling on upper left thigh, (the worst knee), as if it is wet but when I touch the skin it is totally dry! Happens after I have been standing for a couple of hours.Also, sometimes the skin feels sore, but there is no evidence to show. Has anyone had similar feelings?.
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So I have been advised by 2 different oral surgeons I need total joint replacement of both joints.
For those of who have gone through joint replacement, I would really appreciate knowing:
1) what questions I should be asking the surgeons about the surgery, about the outcomes; about post-op care; risks;
2) what your personal exerpience was - just want to know what to expect.
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About 15 months ago I started noticing a strange feeling in my right leg. I could not cross my right foot onto my left knee one day without a strain. A couple of months later I noticed that I was constantly flexing my quad muscles. Shortly after that, my knee would be slightly swollen and not look or feel right after normal daily activities.
This went on for several months with relatively no change and no pain. In time I developed a small limp, but was still not experiencing any pain. Just a limp with some motion limitations.
I finally went to a doctor and was told I strained my IT Band and to stretch and to walk regularly to help it to heal. This was not my issue and neither walking nor stretching helped or worsened the condition (that I know of).
About 5 months ago my limp was very noticeable and I could not even jog. But still no pain. Just limited motion. Although if I forced myself to run, it was painful, but I did not experience any pain day to day.
I went to an orthopedist and had an MRI done and was then diagnosed with synovial osteochondromatosis in the hip. It seemed very strange because any discomfort I was experiencing was in the knee. But the doctor explained it was referred pain for the issue in my hip.
The plan was set to get surgery, but due to family and work obligations I put it off for 5 months. During that time my condition rapidly accelerated. After a month I began experiencing pain in my knee daily. After a couple of months the pain became much worse and I was constantly having using ice and IBU to manage it. In time I could no longer walk without a cane. In the last weeks leading up to my surgery I could no longer use a cane and was only waking when absolutely necessary and only with crutches. I had to take the last 3 week off of work from my desk job because sitting was unbearable.
I have never experienced this type of pain before. I could not sit, stand, walk or even lie down without terrible pain or at best being very uncomfortable. I didn't sleep more than an hour at a time in the last month.
3 days ago I finally got the surgery. They removed hundreds of loose bodies from my hip, some fairly large. I'm not sure on the count or size just yet but will learn that at my next appointment.
Obviously it is too early to really know how successful the surgery was. But I do feel a great deal better on day 3 after the surgery than I did going into the surgery. I actually have less pain today and more movement than I did the day before the procedure! I can bend my knee straight out to about a 60 degree angle. Before surgery I could barley make it up a step and was in serious pain with each stair.
I don't want to get ahead of myself and say that I have been fixed. There is still a lot of motions that I cannot do and I am still very sore from the surgery. Right now it is hard to tell if the limited motion and soreness I am experiencing is from the surgery or not. The doctors say that because things had gotten so bad, I will likely be in physical therapy for up to one year retraining the muscles to function properly again. They also said that there didn't seem to be much damage done to the joint and it does not look like I will need a hip replacement because of it.
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I have now developed a knee Effusion and have tremendous pain. Put onto Celebrex. Do I use crutches again or strap knee? Doctor says i need to rest it as much as possible
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I am a 65 year old female soon to have a L4/L5 Laminectomy with resection of Synovial Cyst (L4/L5) I need more information about the surgery, and what to expect as far as recovery time, etc.
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In January 2013 I started having left leg pains and started taking ibuprofens or store brand pain killers. Over the last 3 months the pain has become chronic, numbness in my big toe and foot, tingling, and pain in my buttock. This is only happening in my left leg. To make a LONG story short. The MRI showed a cyst pressing against my spine causing the pain. Initially my chiropractor thought is was a disc issue causing my sciatic nerve issues. My neurologist suggested a laminectomy Surgery however his concern was if I need fusion. I had an x-ray done that indicated there is some slipping. The neurologist gave me his best guestimation of how long that area of my back would last without the fusion. If he could have given me a high % that the fusion is necessary I would be at peace with it. Decisions, decisions. I was told the recovery is about 4 -6 weeks and longer with the fusion Do you have any knowledge on either procedure?
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Hello,
I'm new on this board. On October 1st 2015 I had decompression surgery (L2-L4), a laminectomy and removal of a synovial cyst that was very high up on the spine (L2)- it was compressing the cauda equina in a bad way. Since then I have had a lot of nerve pain in my groin (both sides), hamstrings, plus sciatica down my right leg from the hip to the toes (according to the neurosurgeon, this is a 'small hernia' due to stenosis and a trapped nerve on S1/L5/L4 that he will operate on when the pain gets too much for me). Not sure if the sciatica is related to the cauda equina syndrome, but imo the cause of both is spinal stenosis. The nerve pain got less throughout the months (except for the sciatica) but the last weeks it's returning again more, on both sides. I had an MRI done two months ago for the sciatic pain and the doctor saw 'something' on the L2 facet joint that could be a new synovial cyst, or else it's scar tissue, he wasn't sure. My gut feeling is that the cyst is growing back and pressing on the cauda equina again- or could it be that i'm still recovering from the first surgery (now 6 months ago)? I sure hope it's the latter, as it was a big operation and the surgeon said that fusion may be next, as the facet joints move too much and in this way the liquid will keep forming new cysts. Ugh. Mid August I will have a new MRI to see whether the synovial cyst is back or not.
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Impression: Moderate L4/5 disc bulge and a left medial synovial cyst. Significantly compressing the left thecal sac and contributing to moderate central canal and left greater than right lateral stenosis.
I have had progressively worsening low back pain and upper leg and butt pain.
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I had a laminectomy with removal of a synovial cyst exactly 17 days now and feel wonderful. Last weeks follow up visit actually was an eye opener because i found out I was doing too much, like bending for example, and I am really suppose to take it easy so the scar tissue can form a strong bond.
My cyst was large and sitting on the nerve root. As soon as it was removed the compressed nerve popped right back up, all good news.
I am wondering how soon before i can start doing other things besides resting and walking. I understand the golf is not happening for at least another 6 weeks and that's ok, but can I swim or when can i ride a bike?
I have basically no pain aside from a little muscle spasms.
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I have sever back pain and haven't been able to work since August. I am unable to stand, sit or walk for long periods of time. It hurts to sneeze, cough, bend or pick anything up. The pain is constant, stabbing at times and it feels like I have a rock in my spine. They have done facet and epidural injections. I take an anti-inflammatory, muscle relaxer and Norco (3 times a day). They tried to put me on Neurontin but it made me too sick. I have had every test done imaginable and basically what I have is degenerative disk disease with mild broad-base bulge. Bilateral facet arthropathy and ligamentum flavum hypertrophy. Indentation of the thecal sac in L4-L5. L5-S1 bilateral arthropathy. L3-L4 bilateral ligamentum flavum hypertrophy and a left nerve sleeve cyst (synovial cyst).
My surgeon wants to do a foraminotomy because I have radiculopathy on L4-L5 and then do a spinal cord stimulator for the pain. He isn't worried about the cyst...said it isn't the reason for my sever back pain. From what I have been reading, all of my symptoms sound like its the cyst causing at least some of the pain. Am I wrong to second guess his opinion? I just don't want to have these surgeries done and then later down the road turn around and have to have the cyst removed.
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I'm scheduled for surgery next month to remove a synovial cyst in my lower spine. The pain is present only when standing and walking for long periods, but debilitating when it occurs. I've read so much on this site, I thought I would get some of your views.
My neurosurgeon plans to do a laminectomy to reach the cyst which he says is quite large. We debated about whether a fusion is necessary to prevent the cyst from recurring. There is a difference of opinion among surgeons. Two that I've had review my X-rays say I have some degeneration in the disk and should have a fusion. A third says to take the risk and avoid the fusion. Eventually my surgeon convinced me I should have this done in order to return to an active life vs sitting on the couch. He does minimally invasive surgery and does not use a cage or pedicle (sp?) screws as he believes they put too much stress on other disks. Instead he showed me a very simple clamp he has used successfully. Has anyone heard of this - alternative?
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