I've never had a biopsy, so I really cannot advise you.

Some others may come on here. I believe however that all
it will show is that you have axonal damage. This is not really
going to say WHAT is damaging you however.

I'd Google some more. It had been my impression that this sural
biopsy is not done much anymore.

Maybe Glenn will come on with more information. He has had
the skin punch biopsies more than once.

have you been thoroughly tested already? spinal tap? blood tests? skin punch biopsy? emg/ncs? a nerve biopsy is a last resort. very few people who have posted here or that i have talked to in real life have had a nerve biopsy and i can only remember one who had one who said it aided in diagnosis. the fact that the doctor wont tell you what he suspects or is looking for in the nerve biopsy is a red flag as far as im concerned. there are neurologists who specialize in surgery such as nerve biopsies and this is what a number of them push for early in the diagnosis stage.
I was diagnosed with sensory motor axonal PN via emg/ncs and was referred to Columbia Presbyterian Neurology for a further workup. The first thing they wanted to do was a nerve biopsy. Thankfully i found the PN support site that was where the long term posters to this site were prior to going for the biopsy and as a result was tested correctly without the permanent damage which would have been done by a nerve biopsy.

If it were me i would do my research on nerve biopsies and if the doctor still refuses to tell you what he is looking for or suspects I would move on.

Thanks, echoes...

Here is book link...

http://books.google.com/books?id=56q...ed=0CGMQ6AEwCA

Sounds like a money maker to me!

Ask your doctor these questions:

How many of these have you done?

What will it show, and how will you then treat the results?

Did you do a nerve conduction on this nerve already? Was it normal?

I have had the sural nerve biopsy...back in '97. It is NOT done often anymore according my neuro at Hopkins.

I can only relay my experiences and what you may encounter might be different. The procedure of course completely severs the nerve so anything below the area will be numb...guaranteed. I did not have the option for any re-attachment with shunt, so don't know the outcome of that. I also experience significant phantom pain that can (and was) disabling. This lasted for almost a year but did lessen slowly over this time period. To this day I have no feeling from the back of my calf down & around the outside of my foot. Have I gotten used to it? Yes, but it took a while.

I did not have the punch biopsy before the nerve biopsy, and frankly don't think it was widely used at this time ('97). I have since had the punch biopsy twice and suggest you at least ask your doctor WHY he's not considering this first since it's less invasive and provides sufficient information for diagnosis of SFN.

The sural nerve biopsy may provide similar results that a punch biopsy would but neither will tell you what is causing it. I also don't know if the nerve biopsy can actually confirm SFN because they are not looking at the small fibers. Mine (nerve biopsy) showed axonal degeneration, but like MrsD said, it doesn't show why and from what.

Did you ask him about the punch biopsy? What was his reply? Do you have positive EMG or NCS that would indicate large fiber neuropathy?

--as the others here have said, is really only now for very special diagnostic suspicions and indications.

Because of those indications it should also involve a biopsy of muscle tissue as well.

In general, at the very least, it will leave some areas of patchy numbness. That may be worth tolerating if you get a definitive diagnosis and a treatment plan. But, some have reported the standard post-operative complications of surgery (infection, etc.) and the fact that the doctor has a suspicion but doesn't want to tell you is rather disquieting.

Take a look at this--it's a very comprehensive look at how/why a nerve/muscle biopsy might be performed:

http://neuromuscular.wustl.edu/nother/bx.html

A lot of the more common diagnoses, though, might be made with other testing. In my estimation, only a few of the diagnoses listed, mostly very rare ones, quite a number of them hereditary, would require a nerve/muscle biopsy for confirmation. So it would be good if that doctor told you what was being looked for.

for all the responce. Origonally 3+ years ago I had alot of testing that showed nothing. I am hoping that my neurologist will let it slip what they are looking for. An EMT friend told me that he suspects the doctor did not want to throw out assumptions. I don't know. As far as infection. The surgeon said he only does this at Strong memorial in the OR in the most sterel conditions.

Also this has never been suggested before. They may be thinking last resort.

I will do more research on the doctor. everyone so far say's he is very good. Thanks again.

Why don't you ask the doctor what he suspects? I sure would want to know. It doesn't mean you have any of it but I would want to know what his thinking is.

Wow, I read this and there are so many possibliities.

I went to Columbia Presbyterian and had two skin punch biopsies that confirmed smal fiber neuropathy. It was no big deal physically but it was emotionally to finally have an answer. Due to autonomic neuropathy and many allergies to drugs nothing but telling me to take folic acid has happened. I am going back in a couple of weeks in hopes of finding some solutions to the autonomic dysfunction that has slowed me down. SFN and RSD - I can't really tell them apart. Pain is an active ingredient. I had a spinal cord stimulator implanted in my spine over a year ago. I am grateful I did.

I would definitely question the doctor further and seek some testimonies from other patients. I have found I need to do my research first and then go to the doctor. Just this past weekend I was in the hospital. This doctor talked at me the whole time and he wasn't pleased I had been admitted and was quite nasty. I told him to discharge me immediately and then called patient relations and got rid of my anger there which did absolutely no good for the situation other than my having my say. A doctor who doesn't listen or answer questions is one to challenge. May you find the information you need to make the right decision for you.