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Look like DH? Bilateral Itchy Bumpy Elbows


Jane87

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Yaya25 Newbie
On 11/29/2017 at 6:45 AM, Jane87 said:

Hello wise people!

I'm looking for some advice from those in the know. I have a reoccurring elbow rash (bilateral) that comes and goes. First episode about 10 yrs ago at age 20.

It presents as skin coloured bumps that are really itchy on both outer elbows. Over the course of 1 to 2 weeks the bumps may turn pinker and then dry out.

I saw a Dr in the early days and was told it wasn't psoriasis and was possibly caused by leaning on my elbows. ?

After another flare up last week (first in months) I saw a Nurse, who has referred me for a Dr review in a few weeks (earliest available appointment).

In the last 3 years I have also had flare ups of; itchy bumpy fingers, itchy lower back with tiny blister/bumps that turn red and extremely itchy calves with no rash. 

My mum is gluten intolerant with skin & stomach symptoms and has hypothyroidism.

I have attached pics of my elbows from this week, and older pictures of my fingers and back rash.

Any thoughts and comments will be greatly appreciated. Does this look like DH?

PhotoGrid_1511964833749.webp

PhotoGrid_1512065525148.webp

Hi Jane, I know this was written 2 years ago, but do you have an update on your diagnosis? Did you find out the cause of your rashes? Because I HAVE THE EXACT SAME THING! 

  • 1 month later...

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Lea1702 Newbie
On 7/6/2019 at 5:31 PM, Yaya25 said:

Hi Jane, I know this was written 2 years ago, but do you have an update on your diagnosis? Did you find out the cause of your rashes? Because I HAVE THE EXACT SAME THING! 

Hello, I see your post is more recent than the OP in 2017, did you find out anything about this? My daughter has this exact rash. Comes and goes for the last 3 years. Elbows mostly and sometimes knees. She's 6. I have ceoliac in my family, but not us that I know of. Interested to find out more. Thanks.

GFinDC Veteran

Hi Lea,

Jane hasn't been on the forum for a few years.  She also isn't following this thread so she won't know you posted a question for her.

There is lots of info on DH in the forum though.  You might get more response by starting a new thread.

  • 2 weeks later...
Medicmicki67 Newbie
On 9/6/2019 at 7:27 AM, GFinDC said:

Hi Lea,

Jane hasn't been on the forum for a few years.  She also isn't following this thread so she won't know you posted a question for her.

There is lots of info on DH in the forum though.  You might get more response by starting a new thread.

I have the same thing, but no autoimmune or celiac. I find that rubbing handsanitizer on my elbows, up to 4 times a day for about a week usually makes it go away.

  • 1 year later...
Margarita Apprentice

My DH was misdiagnosed as dermatitis Until recently when I put 2 and 2 together and figured out I probably was a Celiac. I confirmed it with the gastroenterologist and the DH never shows up unless I get glutened. So when I see yours I think it's DH.

20210506_071721.webp

20210506_071718.webp

GFinDC Veteran

Welcome to the forum Margarita! :)

Please take a look through the DH (dermatitis herpetiformis) sub-forum for more info on DH.  You may find some helpful info in there.

Margarita Apprentice
2 minutes ago, GFinDC said:

Welcome to the forum Margarita! :)

Please take a look through the DH (dermatitis herpetiformis) sub-forum for more info on DH.  You may find some helpful info in there.

Thank you so much for the warm welcome! I still don't really know anything about forums and sub forums but i'm sure I'll figure it out. I was actually wondering how people have their diagnosis attached under their comments? Could you please help me with that?


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GFinDC Veteran
1 hour ago, Margarita said:

Thank you so much for the warm welcome! I still don't really know anything about forums and sub forums but i'm sure I'll figure it out. I was actually wondering how people have their diagnosis attached under their comments? Could you please help me with that?

Hi Margarita,

It used to be a person could add a signature under their profile.  If you click the down arrow next to your profile picture at top right of the page, and click "settings" you can find the signature option in the left side list.

If you click the "Forums" link in the top blue bar/banner, it will take you to a list of forum sub sections.  Scrolling down that list you can find the technical help sub forum.

https://www.celiac.com/forums/forum/44-boardforum-technical-help/

Thread on setting signature:

https://www.celiac.com/forums/topic/122913-change-signature-information/

 

Margarita Apprentice
21 hours ago, GFinDC said:

Hi Margarita,

It used to be a person could add a signature under their profile.  If you click the down arrow next to your profile picture at top right of the page, and click "settings" you can find the signature option in the left side list.

If you click the "Forums" link in the top blue bar/banner, it will take you to a list of forum sub sections.  Scrolling down that list you can find the technical help sub forum.

https://www.celiac.com/forums/forum/44-boardforum-technical-help/

Thread on setting signature:

https://www.celiac.com/forums/topic/122913-change-signature-information/

 

Thank you for your help!

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    • Aretaeus Cappadocia
      I'm not saying this is what you have, but your description reminds me of Morgellons, which are not very well understood. Here is a review from a reputable source. If it seems similar to your experience, you could raise this question with your Dr.  https://my.clevelandclinic.org/health/diseases/morgellons-disease
    • nancydrewandtheceliacclue
      Hi Trent, no dairy. Other than good quality butter. I have been lactose free for years. No corn, sugar, even seasonings and spices. I don't eat out. I cook my own food.
    • trents
      @nancydrewandtheceliacclue, are you consuming dairy? Not sure if dairy is part of the carnivore diet.
    • nancydrewandtheceliacclue
      Hello Russ! Thank you so much for your reply.  I have not had an antibody test done, ever, relating to gluten. Last year I had an allergy test done via blood draw (as my insurance wouldn't cover the skin test) but this was for pollen and grasses, not food. Even on the blood test I had extremely high levels of reactions to each allergen. Could this seasonal allergy inflammation be contributing to my celiac inflammation? I am so careful, there is no way I could ingest gluten. For example, couple of months ago I tried a cough drop that says it was gluten free. I checked ingredients, it seemed fine. But just taking one of those caused me to have nausea, vomiting, and the same extreme abdominal pain. Have you ever heard of anyone else having symptoms like mine after being diagnosed celiac and strictly gluten free? The last episode I had like this was yesterday, after I ate a certified gluten-free coconut macaroon with a little chocolate on it. I have eaten coconut and chocolate before with no issue,  so I didn't see how I could all of a sudden have such a strong response. 
    • Russ H
      The sensitivity of people with coeliac disease varies greatly between individuals. The generally accepted as safe limit for most people is 10 milligrams per day. This equates to a piece of bread the size of a small pea. Some people report that they are more sensitive than this, but others can very occasionally eat a normal gluten containing meal without reacting. I don't think that touching or throwing bread around would lead to you ingesting enough to cause a reaction. There are case reports of farmers with coeliac disease reacting to the dust from gluten-containing animal feed but they were inhaling large amounts of dust over a long period of time in barns. Perhaps you episodes are caused by a reaction to something other than gluten? Have you had your antibody levels checked to see whether you are still being exposed to gluten?
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