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Knuckle Pads
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11/22/2009 14:55
Michael916 
11/22/2009 14:55
Michael916 
Knuckle Pads

I have had dupuytren's in my right hand for some years now. (All four of my brothers have it and my father had it as well). It progressed slowly for years but within the last year or so it has accelerated. The ring finger is now at about 35%. That I am dealing with. My plan is to have NA at some point.
Within the last few months, though, knuckle pads (on my middle and ring finger on my right hand; and on my little finger on my left hand) have emerged and are getting bigger. A hand surgeon xrayed and said that there is no sign of arthritis. I am quite sure that it is the duputren's causing the knuckle pads. They are very painful and depending on how I am using my hands, the pain can be quite intense. I would like any advice readers have to reduce the pain or lessen the size of the pads. I would rather not take medication constantly for the pain but am at a loss for what else to do. From what I have read, surgery is inneffective in the long run. Thank you.
Michael

12/01/2009 01:36
homeboymi 
12/01/2009 01:36
homeboymi 

Re: Knuckle Pads

Michael,

I had a knuckle pad on my right ring finger so large I couldn't get my ring on. This was about 30 years ago. Whenever I bumped the knuckle, it really, really hurt. It lasted about 10 years and then it went down. I still have a small pad on this knuckle but I can wear my ring again. Hope the same happens for you. By the way, I have knuckle pads on other fingers but they don't hurt or bother me.

12/02/2009 21:07
kcc 
12/02/2009 21:07
kcc 

Re: Knuckle Pads

I was diagnosed with DD today. I sought out a hand specialist because of the painful knots on my PIP joints. I had some for 3 years, caused some pain but manageable - as you say, no more door knocking. Recently I have had another one pop up, and it is painful and sometimes sensitive to touch.
Doctor said they are knuckle pads, and I have DD. He pointed out the cords in both hands, which I had thought were tendons. Also, I have a couple of lumps on the palmar side of PIP joints.
So far, no contractures.
He also said only about 1 out of 300 patients he sees with DD have knuckle pads.
If mine doesn't progress, I think I can deal with the knuckle pads.

12/03/2009 02:39
LMM

not registered

12/03/2009 02:39
LMM

not registered

Re: Knuckle Pads

Does anyone know of women with DD as I am 53 and have just discovered that the contractured tendon and lumps in my palm under the 4th digit must be Dupuytrens. Is there a good website to read about stats on this?

12/03/2009 02:40
LMM

not registered

12/03/2009 02:40
LMM

not registered

Re: Knuckle Pads

Sorry I am a knucklehead - just realized I am on a good website for the info required.

12/03/2009 02:56
kcc 
12/03/2009 02:56
kcc 

Re: Knuckle Pads

Hi LMM,

I am 52 year old woman, and I have DD. I don't know of any family history, but that info is limited for me. Diagnosed today. See previous post.

12/03/2009 12:40
BobbieJo5 
12/03/2009 12:40
BobbieJo5 
Re: Knuckle Pads

I'm female, 50-something, with Dupuytren's. For right now, the cord has been reduced by PT (stretching, US, etc). When I wake up in the morning, my fingers are stiff. I can't fully close my fist. All of this does not prevent me from my daily chores. I even saw Dupuytren's mentioned on the local news last night! Had I not been sitting down, I would have fallen down! I've never seen this mentioned in any local media form.

12/03/2009 13:45
lori 
12/03/2009 13:45
lori 
Re: Knuckle Pads

I was diagnosed with DD at age 53 and am female. Started as a tender spot in my palm, then a hard painful lump. Mine progressed to a cord, puckering, intense pain, within 6 months. I finished RT last August and highly recommend it. You can't see the cord but can feel it under the surface of my palm. Still have the nodule and if I hit it, it hurts. A lttle dry skin in the radiated area. Have gotten back most of the use of my hand. If I pick up something heavy I can still feel a weakness in my hand. There are quite a few women on this forum in our age bracket that have DD. No known family history until I was dignosed. Grandmother and aunt had it but we all thought it was arthritis because they developed it in their late 70's to early 80's. If you have any questions let me know.

Lori

12/07/2009 23:32
crt 
12/07/2009 23:32
crt 
Re: Knuckle Pads

Michael,

I have had knuckle pads (on all fingers) since my teenage years (i'm now 57), plus Ledderhose and more recently DD.

I had surgery on one knuckle when it first appeared. The surgery made the lump much larger, reduced movement and made it more sensitive and painful. However, that was a very long time ago and surgery may have improved, so I shouldn't take my experience in isolation as a guide.

However, whilst the pads have been annoying, they have not significantly affected my life. In more recent years the size of the pads has reduced (this happened with my mother as well).

We all have different experiences, but if you are lucky enough not to be have painful knuckles in every day usage of your hands (if you knock them, of course they will be painful), then I would suggest ignoring them!

Good luck, Chris.

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contractured   diagnosed   experiences   accelerated   Knuckle   progressed   stretching   knucklehead   Grandmother   painful   experience   50-something   dupuytren   contractures   Ledderhose   manageable   Dupuytrens   mentioned   significantly   inneffective