Laminectomy With Resection Of Synovial Cyst - Experience?
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.
View 1 RepliesArthritis :: Synovial Effusion But No Joint Damage ?
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.
Laminectomy And Synovial Cyst - Reviews Or Feedback?
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?
View 14 RepliesFailed Laminectomy And Removal Of A Synovial Cyst?
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.
MRI: L4-L5 Bulge, Left Medial Synovial Cyst
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.
Walking With Arthritis, Stenosis And Synovial Cysts
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.
Lumbar Synovial Cyst Removed - Recovery Time?
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.
Lumbar Synovial Cyst Causing My Back Pain?
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.
Lumbar Synovial Cyst Removal - Clamp Vs Fusion?
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?
Recovery Time? Lumbar 4-5 Laminectomy With Synovial Cyst Removal
i am having a posterior lumbar 4-5 laminectomy with synovial cyst removal on August 27,2015. I have a 5 day trip to Germany planned 6 &1/2 weeks later.
I now know the recovery to be longer than the one week I had thought. I know it is at least 6 weeks, after my pre surgery intake with the wonderful nurse I have. Does anyone have feedback about a 8 hour plane ride to Europe with only 6 weeks recovery time? Thanks
Spinal Cord :: Synovial Cyst Is Groin Pain - Symptoms?
I was diagnosed as having a synovial cyst by a neuropsychiatrist. I had a procedure where he went in and drained the cyst along with that I had a steroid injection. Apparently he did not get much out of the cyst. The pathology report came back negative on what he did manage to get out.
On day two post procedure the pain starting coming back. Each day the pain level increased to where I am now a level 8 and sometime 9 and can barely stand the pain. My lower right back just above the buttock feels like there is pressure and is very achy. The deep achy pain goes into my right buttock and wraps around the lower groin area. The achy pain goes down my right leg and into my foot. It is a pulsating deep ache and I can hardly stand it. It also feels numb at times and I get pins and needle tingling. When I get up from laying down or sometimes sitting (when I can sit) I get this sharp excruciating pain in my right groin that doubles me over. I have to stay still in the doubled over position to let it subside before I can straighten up and walk. Sometimes the groin pain just hits me out of nowhere when I am standing.
On my follow up visit with my physiatrist he recommended I have a consult with a neuro spine surgeon. My appointment with the surgeon is in a couple of days. I feel very fortunate to get into see this surgeon who is very hard to get in to see. He is rated as "one of the best" in a very large healthcare system where I work.
I am taking 1500mg of gabapentin along with 6 ibuprofen a day. I am also taking hydrocodone. I fight the pain and only take on the average one pain pill a day because I don't like the groggy feeling.
My question is, has anyone else with a synovial cyst had all of these symptoms? Is the groin pain related to the compression on the nerve from the cyst. I appreciate any feedback and would love to hear from someone who has had these symptoms.
Back Issues :: Synovial Cyst Removal 10 Days Post Op - Numbness In Foot?
I am ten days post cyst surgery, no fusion, just cyst removal. I have some numbness still in my foot. Is that normal?
View 1 RepliesENT :: Day 1 Experience After Stapedectomy
After the usual IV insertion, walking to OR and walking up rather groggy, I must say the first few hours were strange. Having limited hearing in my right for the past 7 years ( and getting worse) I decided to go for the operation.
My mouth and throat were very dry (11am operation with no food or drink in 12 hours) and deep breathing was challenging. I was encouraged to take deep breaths to clear anything from my lungs. My OP ear was full of cotton and gauze so hearing from that side was nada. My good ear was very amplified like I had a microphone inside my mouth, I would scratch my head and it was LOUD. I was discharged after I could stand without aid and at home crashing on the couch.
I had a protein shake and a bowl of hot soup and felt very stable with no dizzy spells or balance issues, but still the amplification inside my head. I had ringing tones on my OP ear on and off but no pain. If I plugged my good ear I could hear nothing but the ringing.
Five hours now and I feel good but I can hear everything around me, the talking , the tv, things very far away are very clear. My dog barked right beside me and I nearly jumped off my chair, scared me. It was loud. I used to watch tv on 65 volume now it's at 40 volume.
Pompholyx Sharing My Experience
I am a 29-year-old male of Asian decent (Taiwanese) living in the United States. My first episode happened last November and has continued ever since. It was diagnosed by a dermatologist this April. The worst that I've suffered was when all my fingers and palms, toes and soles were covered with small itchy blisters. Currently my hands are 90% pompholyx-free (yay!).
I think there are three major factors that contribute to the outbreak (environmental, mental, and diet), and I'll explain each in more detail:
Environmental: During dry winter seasons, I develop skin rashes all around my body (guys hate lotion), I think if dry skin can contribute to skin rashes, it probably can contribute to pompholyx outbreak as well.
Solution: Make sure your body is well moisturized, I really don't enjoy the oily sensation, but it sure beats waking up to the itch in the middle of the night! Cetaphil cream (not lotion) work very well for me. Stock up when they're on sale!
Mental+Sleep: I was unemployed when the first episode occurred, and I think stress has a lot to do with it. Also, make sure you sleep at least 7 hours a day, and try to relax and think positive thoughts as much as you can.
Solution: I just try to be grateful of what I have... there are people out there who are suffering diseases 1000x worse than pompholyx or being unemployed....
Diet: The dermatologist told me to cut out chocolate and nuts (especially peanuts) completely. It was HARD. But I started about 2 weeks ago, and it's been working so far. There was a scientific study about the possibility of chromium in chocolate that induced a flare up (from breast milk)
http://www.ncbi.nlm.nih.gov/pubmed/17671414
For nerds like me, you can check it out (be aware though, it's just a sample size of 1!)
solution: see above, you can cut out coffee too, but that will be too hard for me.
Medication:
As a prophylaxis, I take a 180mg fexofenadine every night. In addition, when you see (or feel) small blisters starting to accumulate, there are two topical steroids that I use.
0.05% clobetasol propionate (GSK markets it as Dermovate), ointment form
0.5mg/gm fluocinonide, cream form
http://img.medscape.com/fullsize/migrated/551/352/dn551352.tab4.gif
clobetasol is listed as class 1, very high potency steroid, and fluocinonide is listed as class2, high potency steroid. My dermatologist assured me that applications to the extremities (fingers, toes) will not cause a lot of absorption to the body, so you can be very generous in your application.
I also take multi-vitamins. My dad (who's an MD) told me Asians do not absorb B-vitamins very well, so it's important to supplement with either B-complex or B-12 vitamins.
This is a pesky condition to have...
Lupus :: Any Experience With Seizures?
I was wondering if anyone had any experience with seizures with their lupus. I had one seizure last see summer before I was diagnosed with RA. I have been told by rheumatologist that I have RA with overlapping lupus symptoms, no positive lupus labs. My question is about the seizure, it was not a grand mal type, no convulsing but I did lose consciousness for almost 5 minutes. Is this a lupus sign. They found NO medical reason at the time for this.
View 2 RepliesFlexible Cystoscopy? Any Experience?
I am 39 years old and since 10 months cystitis is been part of my life. I took many antibiotic and resulted positive to 2 urine test with the “Escherichia Coli” bacterium. I went to the specialist and had an ultrasound, which was normal but now he is insisting on having the flexible cystoscopy which consist in inserting a small tube with a camera inside the bladder to make sure that nothing is obstructing the urine tract such a stones, small extra tissues etc.
Wouldn’t the ultrasound identify these if any? Has any of you done this test (Flexible Cystoscopy)?
Does any of you managed to have an Antibiogram test (or ABG) which allow to identify what antibiotic is right for that type of bacteria?
Had Sigmoidoscopy - A Good Experience
it's not as bad you people think. I must admit I was fearing it a lot and this might be one of the reasons why I overreacted to the discomfort felt by the pumping of air to distend the bowels. There are no nerves in the bowels so you cannot feel any pain. Proof of this was when they did a random biopsy on me and ripped out samples of tissue from my bowels (as I watched on the screen). There was no pain at all apart from the odd sensation which felt like someone flicking a rubber band inside my gut.
It's always fear of the unknown which scares of most. After the procedure the only pain I really experienced was wind as they had probably pumped the world's gas supply into me (ok so I might have exaggerated a bit) but seriously, it's not all that bad and you'll feel ok right after one big release.
My 7 Years Experience With Implanon
I have had the implanon since I was 17 (now 24) and it has served me well...most of the time. I am actually considering having it removed because I have headaches five out of seven days a week; have gained about four kilos, which I cannot lose despite a healthy lifestyle and diet; I am moody; and I have trouble sleeping.
Most of these things I thought were just normal women's behaviour, but after speaking with many other women who have since gone off various other contraception, it has been brought to my attention, this all might be a side effect.
I have not had a period since having it inserted -except when it was removed after the three years while waiting to have it inserted again- which has been great. Despite this my main concern are the constant headaches, so I am having it removed and staying off contraception like this for a while to see what changes may occur.
Experience With SI Joint Injections?
Anyone have experience with SI joint injections?
I have been dealing with pain (from nagging to disabling) for almost a year. A year ago, the pain slowly progressed to the point that any position was uncomfortable...sitting, standing, walking, sleeping was impossible (for some reason the pain seems worst at night). At that point, I called my spine surgeon (had a lumbar burst fracture 5 years ago so already had a doctor ), but the first available appointment was a month out...I scheduled the appointment and went to the ER after not sleeping any more than an hour or two for several weeks in a row due to pain. They gave me a Toradol injection, muscle relaxers, and Vicodin. I went home thinking that I would finally sleep...WRONG! All those drugs did nothing to stop the pain! I struggled through the next few weeks until my appointment. My doctor's first guess was a disc problem due to my history; however, MRI showed healthy discs and fracture site looking as good as a burst fracture can After a few more tests, he diagnosed me with an SI joint problem and put me on Relafen for 6 weeks to control inflammation. After 3 weeks, I did see improvement...The pain returned to the "annoying" level. Since that time, the pain has been up and down...Always there, not always awful, but sometimes miserable for weeks at a time. I had a foot/ankle reconstruction in November and had a HUGE flair up after that...I realized that I really had an issue when my back pain was keeping me awake at night, not the heel bone that had been sawed into three chunks! I was hoping this problem would just disappear as mysteriously as it began; but, unfortunately, it looks like it's here to stay. My doctor has recommended an SI joint injection as the next step.
Has anyone had success with SI joint injections? My typical symptoms are left side lower back, hip, and thigh pain from just annoying to feeling like my bones are disintegrating...that's the best description I can come up with I also have a lot of muscle soreness in those areas.
How was the "injection experience?" I've had cortisone injections in my foot before, and they were not pleasant...So, I'm definitely not excited about this. I have a high pain tolerance and have dealt with a lot of medical procedures, but something about someone sticking a big needle in my back doesn't give me a warm, fuzzy feeling.
Did you have increased pain for a few days following the injection? After the ones in my foot, I had fairly severe pain for several days...I think they called it a cortisone flair.