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-   -   Has anyone found MRI neurography of the brachial plexus helpful in diagnosing TOS (https://www.neurotalk.org/thoracic-outlet-syndrome/210414-found-mri-neurography-brachial-plexus-helpful-diagnosing-tos.html)

Hope526 10-03-2014 12:56 AM

Has anyone found MRI neurography of the brachial plexus helpful in diagnosing TOS
 
I'm wondering if anyone has had success in diagnosing compression sites with a Neurography of the brachial plexus? I was told that it is ineffective because without compression the nerves have a normal appearance.

I have not been given an official diagnosis of TOS although I have been exhibiting all of the symptoms for more than a year. The thing that is keeping my docs hesitant to label me with the TOS diagnosis is because I did not have significant improvement of my symptoms with the botox injection to my anterior scalene and pec minor. Just wondering if it might help in the diagnosis and with treatment.

H20man 10-03-2014 09:41 PM

Quote:

Originally Posted by Hope526 (Post 1100847)
I'm wondering if anyone has had success in diagnosing compression sites with a Neurography of the brachial plexus? I was told that it is ineffective because without compression the nerves have a normal appearance.

I have not been given an official diagnosis of TOS although I have been exhibiting all of the symptoms for more than a year. The thing that is keeping my docs hesitant to label me with the TOS diagnosis is because I did not have significant improvement of my symptoms with the botox injection to my anterior scalene and pec minor. Just wondering if it might help in the diagnosis and with treatment.

I had one at Johns Hopkins. They didn't find anything in the MRI. Most all of my tests were negative expect for my EMG and nerve conduction. I just had a first rib resection 2 weeks ago. Still too early to tell how well it worked though. It's worth being thorough and getting all of the tests done you can. I spent 2 years going through everything before deciding on surgery.

Hope526 10-03-2014 11:12 PM

Quote:

Originally Posted by H20man (Post 1101031)
I had one at Johns Hopkins. They didn't find anything in the MRI. Most all of my tests were negative expect for my EMG and nerve conduction. I just had a first rib resection 2 weeks ago. Still too early to tell how well it worked though. It's worth being thorough and getting all of the tests done you can. I spent 2 years going through everything before deciding on surgery.

I hope your surgery is very sucessful!:) My Dr is pretty certain that the MRN won't show anything but I can't help but try everything. Did they try botox injections on you before the surgery? If so did they relieve your symptoms? The vascular surgeon I saw is recommending surgery if all else fails.

cyclist 10-04-2014 03:37 PM

Hi Hope -
I read your introduction (in your 1st post) and gosh...your symptoms and history really sound like TOS to me. Are you seeing a doctor who is highly specialized in TOS? I would think that an experienced TOS specialist would diagnosis you on the spot based on your symptoms and history alone.

Otherwise, I wanted to mention, that my doctor told me that if the scalenes are highly scarred, they become almost tendon-like, and the Botox will not provide the chemodenervation and relaxation effect that would otherwise occur in normal muscle. Therefore, Botox will not work in these cases, even though the scalenes are the problem. Given that you've had 5 MVAs, with 4 of them being potential whiplash incidents... perhaps this is why the Botox is not working for you.

Also, I've had an MRI/MRN of the brachial plexus. I have one-sided symptoms and we were "hoping" to find that the anterior scalene muscle had hypertrophied/enlarged on the symptomatic side, compared to the non-symptomatic side. This did not show up on the MRI. Instead, we found that the brachial plexus is exiting the scalene triangle high up (in the narrower part), with the upper trunk particularly high. It's an interesting finding since I tend to show more upper trunk symptoms. However, while such anatomy is thought to be a predisposing factor -- it is far from definitively diagnostic.

IMHO... I think you should go forward w/ the MRI/MRN and also seek a second opinion from another TOS specialist, even if you have to travel to get to one.

Hope this is helpful, and best of luck to you.

jkl626 10-05-2014 03:06 PM

HI
My BP mri showed neural edema which is irritation of the nerves. This was helpful in that was just one of the things pointing to a TOS diagnosis for me. The other was a scalene block (successful) but highly subjective and I wasn't in tremendous pain that day) and a physical exam by 3 different doctors who independently gave me a TOS diagnosis .Unfortunately botox didnt help me either. I am not pursuing surgery at the moment although had 3 consultations.I have had a little bit of success with PT, Trigger point injections and Lyrica. Occaisional Tramadol or a muscle relaxant. Still not enough for me to go back to work or be normal.
JKL

16rhonda 10-05-2014 11:10 PM

re : emg/ncs
 
Quote:

Originally Posted by H20man (Post 1101031)
I had one at Johns Hopkins. They didn't find anything in the MRI. Most all of my tests were negative expect for my EMG and nerve conduction. I just had a first rib resection 2 weeks ago. Still too early to tell how well it worked though. It's worth being thorough and getting all of the tests done you can. I spent 2 years going through everything before deciding on surgery.

Hi there, hope your recovery goes well!
Just wondering what nerves showed abnormal on your emg tests? How long did u have your sx bf surgery?

Thanks

Hope526 10-06-2014 12:32 AM

Quote:

Originally Posted by cyclist (Post 1101182)
Hi Hope -
I read your introduction (in your 1st post) and gosh...your symptoms and history really sound like TOS to me. Are you seeing a doctor who is highly specialized in TOS? I would think that an experienced TOS specialist would diagnosis you on the spot based on your symptoms and history alone.

Otherwise, I wanted to mention, that my doctor told me that if the scalenes are highly scarred, they become almost tendon-like, and the Botox will not provide the chemodenervation and relaxation effect that would otherwise occur in normal muscle. Therefore, Botox will not work in these cases, even though the scalenes are the problem. Given that you've had 5 MVAs, with 4 of them being potential whiplash incidents... perhaps this is why the Botox is not working for you.

Also, I've had an MRI/MRN of the brachial plexus. I have one-sided symptoms and we were "hoping" to find that the anterior scalene muscle had hypertrophied/enlarged on the symptomatic side, compared to the non-symptomatic side. This did not show up on the MRI. Instead, we found that the brachial plexus is exiting the scalene triangle high up (in the narrower part), with the upper trunk particularly high. It's an interesting finding since I tend to show more upper trunk symptoms. However, while such anatomy is thought to be a predisposing factor -- it is far from definitively diagnostic.

IMHO... I think you should go forward w/ the MRI/MRN and also seek a second opinion from another TOS specialist, even if you have to travel to get to one.

Hope this is helpful, and best of luck to you.

Thanks cyclist. What you said about the botox not working due to scarring makes perfect sense to me. I did see a TOS specialist who originally diagnosed me with it but after the botox injections failed to help he said he can't definitively say that I have TOS. Another symptom I have that doesn't seem to be as common with TOS is mid to upper back pain. I'm not sure what that's all about.

I'm pretty desperate right now and willing to try anything. I'm going to try rolfing next to see if that will bring any relief. I'm curious to know what type of treatment has worked best for you?

I appreciate all of your input and I am going to have the MRN in a few weeks. I'm curious to see what, if anything, it will show.

Take care:)

Hope526 10-06-2014 12:44 AM

Quote:

Originally Posted by jkl626 (Post 1101339)
HI
My BP mri showed neural edema which is irritation of the nerves. This was helpful in that was just one of the things pointing to a TOS diagnosis for me. The other was a scalene block (successful) but highly subjective and I wasn't in tremendous pain that day) and a physical exam by 3 different doctors who independently gave me a TOS diagnosis .Unfortunately botox didnt help me either. I am not pursuing surgery at the moment although had 3 consultations.I have had a little bit of success with PT, Trigger point injections and Lyrica. Occaisional Tramadol or a muscle relaxant. Still not enough for me to go back to work or be normal.
JKL

Sorry to hear that JKL. I totally understand your frustration. I know the feeling of wanting and hoping so badly for something to take the symptoms of this awful syndrome away. I'm curious to know what they are using for your trigger point injections? Do they think that your TOS is due to your scalenes? Which muscles did they do the botox in?
Have you tried chiropractic before? I have been doing it for a few months. It hasn't helped with my nerve issues but it has given me significant relief with my mid-upper back pain.

Hope you find some relief soon:)

cyclist 10-10-2014 01:41 PM

Quote:

Originally Posted by Hope526 (Post 1101394)
Thanks cyclist. What you said about the botox not working due to scarring makes perfect sense to me. I did see a TOS specialist who originally diagnosed me with it but after the botox injections failed to help he said he can't definitively say that I have TOS. Another symptom I have that doesn't seem to be as common with TOS is mid to upper back pain. I'm not sure what that's all about.

I'm pretty desperate right now and willing to try anything. I'm going to try rolfing next to see if that will bring any relief. I'm curious to know what type of treatment has worked best for you?

I appreciate all of your input and I am going to have the MRN in a few weeks. I'm curious to see what, if anything, it will show.

Take care:)

Hey Hope - I think upper back pain, particularly around the scapula / shoulder blades, is pretty common. Otherwise, I'll send you a PM (personal message) to answer your question.

ShaggyChic_1201 10-11-2014 08:33 PM

My MRN did show signs of damage
 
...and it was so useful in validating what I had been saying all along...it hurt here, there and there. 8 years of people telling me it was all in my head and all of a sudden I had proof in black & white. I wanted to take those images and show them to everyone!

Good luck with your surgery!
:hug:

jkl626 10-15-2014 07:06 PM

Quote:

Originally Posted by Hope526 (Post 1101395)
Sorry to hear that JKL. I totally understand your frustration. I know the feeling of wanting and hoping so badly for something to take the symptoms of this awful syndrome away. I'm curious to know what they are using for your trigger point injections? Do they think that your TOS is due to your scalenes? Which muscles did they do the botox in?
Have you tried chiropractic before? I have been doing it for a few months. It hasn't helped with my nerve issues but it has given me significant relief with my mid-upper back pain.

Hope you find some relief soon:)

I do cortizone every few months and lidocaine with vit b and traumeel inbetween.Today I had injections in my rib joint near my scalpula. I dodnt think my TOS is due to my scalenes but who knows? I had botox in about 8 different muscles. had a bad reaction to it. What kind of chiropractor do you see? What type of adujstments? Thanks

Eight 10-21-2014 04:36 AM

Quote:

Originally Posted by Hope526 (Post 1101394)
Thanks cyclist. What you said about the botox not working due to scarring makes perfect sense to me. I did see a TOS specialist who originally diagnosed me with it but after the botox injections failed to help he said he can't definitively say that I have TOS. Another symptom I have that doesn't seem to be as common with TOS is mid to upper back pain. I'm not sure what that's all about.

I'm pretty desperate right now and willing to try anything. I'm going to try rolfing next to see if that will bring any relief. I'm curious to know what type of treatment has worked best for you?

I appreciate all of your input and I am going to have the MRN in a few weeks. I'm curious to see what, if anything, it will show.

Take care:)


Upper back or shoulder pain was one of my main problems for the first ten years.

Hope526 10-23-2014 01:42 AM

Quote:

Originally Posted by jkl626 (Post 1103269)
I do cortizone every few months and lidocaine with vit b and traumeel inbetween.Today I had injections in my rib joint near my scalpula. I dodnt think my TOS is due to my scalenes but who knows? I had botox in about 8 different muscles. had a bad reaction to it. What kind of chiropractor do you see? What type of adujstments? Thanks

I called around until I found a chiro in my area that has had success in treating TOS patients. My chiro uses the activator method. He is only allowed to work on my thoracic area and right arm. Those are the only areas that the insurance have authorized.

Jomar 10-23-2014 01:18 PM

So chiro can't work on your neck , arms, elbows or pec minor at all?

Is that a work comp ins restriction or who set the restriction ?

If you need an adjustment somewhere else to help overall healing that restriction is going to limit your progress..:confused:

Did chiro try to send his own evaluation/assessment to get restriction changed?

Hope526 11-19-2014 01:23 AM

Quote:

Originally Posted by Jo*mar (Post 1104671)
So chiro can't work on your neck , arms, elbows or pec minor at all?

Is that a work comp ins restriction or who set the restriction ?

If you need an adjustment somewhere else to help overall healing that restriction is going to limit your progress..:confused:

Did chiro try to send his own evaluation/assessment to get restriction changed?

Yes Jo*mar unfortunately it is a work comp restriction:( I have been trying to get my neck and left arm added to the claim for 2 1/2 months. I am still waiting for an answer. It is extremely frustrating for me and my chiro because it is obvious that I need those areas to be worked on.

Hope526 11-19-2014 01:38 AM

Quote:

Originally Posted by Hope526 (Post 1100847)
I'm wondering if anyone has had success in diagnosing compression sites with a Neurography of the brachial plexus? I was told that it is ineffective because without compression the nerves have a normal appearance.

I have not been given an official diagnosis of TOS although I have been exhibiting all of the symptoms for more than a year. The thing that is keeping my docs hesitant to label me with the TOS diagnosis is because I did not have significant improvement of my symptoms with the botox injection to my anterior scalene and pec minor. Just wondering if it might help in the diagnosis and with treatment.


I ended up having my MRN and it showed "increased signal in the right proximal and distal plexus and increased signal in the posterior left plexus." It does not give any indication of what muscles are causing this constriction. My understanding is that the increased signal is showing there is edema. Is anyone familiar with MRI and can help me with this. I would really like to know what is contributing to my TOS. I'm going to see a new Dr in the seattle area in a few days. Does anyone have any suggestions on treatment recommendations?? Thanks for your help:)


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