Get email alerts Get Celiac.com E-mail Alerts  




Celiac.com Sponsor:
Celiac.com Sponsor:




Ads by Google:






   Get email alerts  Subscribe to FREE Celiac.com email alerts

Dh Or Psoriasis?
0

9 posts in this topic

I've read everywhere that DH is extremely itchy, but mine is only itchy when it first appears. It usually starts off as a small blister (which is itchy) but once the blister goes, it's not itchy at all. My mum thinks it's psoriasis but I'm not sure. I don't seem to get it really bad either, just small patches.

This was in July 2012:

http://i49.tinypic.com/34pdl5t.jpg

http://i48.tinypic.com/21dphm8.jpg

This how it usually starts, just a tiny blister type spot:

http://i47.tinypic.com/d4s8.jpg

This is from today:

http://i50.tinypic.com/27zdgqo.jpg

I've also got it on my face at the moment, but didn't really want to take a picture. I only seem to get it on my left hand/arm, legs and face but recently had a patch on my tail bone.

Any information/advice would be greatly appreciated. :)

0

Share this post


Link to post
Share on other sites


Ads by Google:

Looks a lot like dh to me. I don't believe psoriasis blisters. Does yours burn or sting? Tail bone is a classic place for dh to present. You might be lucky so far in that it doesn't drive you nuts itching ---- yet. How long do the lesions usually last before they heal?

Oh, gee, I see now you are dx'd celiac ---- in that case you have dh. You've been gluten-free since 2011 ---- that explains why it doesn't drive you bonkers itching. You are getting cc'd somewhere & that's why the dh is showing up. Go over everything --- everything & try to figure out where the cc is coming from. DH is very, very sensitive to the smallest amount of gluten.

0

Share this post


Link to post
Share on other sites

Hmm, looks somewhat like DH but if you think you've been pretty strict about your diet, it also could be something else. My psoriasis started after I went gluten-free. I also get little blisters like that on my hands (and nowhere else) occasionally but It is NOT DH. Anyway, a decent dermatologist should be able to tell pretty easily.

richard

0

Share this post


Link to post
Share on other sites

I have palmoplantar pustular psoriasis. It only shows up on the palms of my hands and around the heels and bottoms of my feet. There is also a generalized pustular psoriasis that can show up on any part of the body. In both cases, the pustules look like whithead pimples. After a day or three they turn into little red spots. As they heal, the skin will crack and peel.

If your pustules don't look like whitehead pimples, that's not what you have.

0

Share this post


Link to post
Share on other sites

Looks a lot like dh to me. I don't believe psoriasis blisters. Does yours burn or sting? Tail bone is a classic place for dh to present. You might be lucky so far in that it doesn't drive you nuts itching ---- yet. How long do the lesions usually last before they heal?

Oh, gee, I see now you are dx'd celiac ---- in that case you have dh. You've been gluten-free since 2011 ---- that explains why it doesn't drive you bonkers itching. You are getting cc'd somewhere & that's why the dh is showing up. Go over everything --- everything & try to figure out where the cc is coming from. DH is very, very sensitive to the smallest amount of gluten.

It burns as the blister appears but as soon as the blister goes and the "rash" appears, it seems to be fine. The patch on tail bone, however, is extremely itchy - especially at night. They take a long time to heal (4-6 weeks) but I generally take ages to heal anyway.

I had some BBQ Rib Doritos at the weekend and I think that's where the CC came from - there's no gluten containing ingredients but they're made in a factory that handles gluten. I know I shouldn't have eaten them, but I guess I'll learn from my mistakes!

Hmm, looks somewhat like DH but if you think you've been pretty strict about your diet, it also could be something else. My psoriasis started after I went gluten-free. I also get little blisters like that on my hands (and nowhere else) occasionally but It is NOT DH. Anyway, a decent dermatologist should be able to tell pretty easily.

richard

As I said to the above poster, I'm pretty sure it was the BBQ Rib Doritos that I was CC'd with. My mum and a bunch of my cousins have psoriasis so that's why I assumed it was that, but with the Coeliac I thought I'd get a few opinions. I guess if it gets worse, I'll see a dermatologist. Thanks!

I have palmoplantar pustular psoriasis. It only shows up on the palms of my hands and around the heels and bottoms of my feet. There is also a generalized pustular psoriasis that can show up on any part of the body. In both cases, the pustules look like whithead pimples. After a day or three they turn into little red spots. As they heal, the skin will crack and peel.

If your pustules don't look like whitehead pimples, that's not what you have.

I looked up palmoplantar pustular psoriasis and it doesn't look like that at all. Looks very painful though, I feel for you!

0

Share this post


Link to post
Share on other sites




I looked up palmoplantar pustular psoriasis and it doesn't look like that at all. Looks very painful though, I feel for you!

Thanks. It is very painful, but the good news is that as long as I stay away from gluten, soy, most forms of corn, and foods high in salicylates, it goes away completely. :)

0

Share this post


Link to post
Share on other sites

Thanks. It is very painful, but the good news is that as long as I stay away from gluten, soy, most forms of corn, and foods high in salicylates, it goes away completely. :)

I'm glad you're able to prevent it. :)

0

Share this post


Link to post
Share on other sites

I have had spots like those too. My blisters are long gone, but my skin still itches like crazy. I wish my skin did not itch so much. My skin now peels and is very dry. I have been mis-diagnosed with Psoriasis several times. A skin biopsy in one spot done last year did show a small amount of Psoriasis once. But my next dermatologist said it was definitely not Psoriasis. I have several friends with Psoriasis, and none of my skin areas look like theirs do. I am puzzled as to what is really going on. I am thinking it is just a form of Gluten Intolerance.

0

Share this post


Link to post
Share on other sites

Psoriasis takes many different forms. Pustular, guttate, etc., etc. I suppose it is theoretcally possible to have both psoriasis and DH, although usually one seems to have one or the other. Have you looked at pictures of all the different forms of psoriasis and of DH? Generally, looking at these pictures, you can find something that matches what yours looks like. Psoriasis does not tend to scar; DH does tend to scar although there are variations that do not leave scarring. Psoriasis itches like cracy but generally does not hurt; DH generally does both. Do some googling and see what you can come up with is my best advice.

0

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!


Register a new account

Sign in

Already have an account? Sign in here.


Sign In Now
0

  • Forum Statistics

    • Total Topics
      104,642
    • Total Posts
      921,568
  • Topics

  • Posts

    • I was only asking because when ferritin is low that you can experience hair loss/fatigue etc. even if your other iron levels are in range. This just happened to me so I thought I would share just in case it helps you. Ferritin should be above 50 to be optimal, not just "in range."  I've been on iron supplements and much better now. This may not be your problem at all, but I would have them check your ferritin levels. Low iron or anemia is common with celiac. The ferritin test is measuring how much iron is stored in your body. FYi: Iron binding capacity is really telling you how much protein your liver is making in order to carry that iron around. Usually, iron binding capacity will be higher in the range when iron is low. Edit: Also my blood pressure was low when my ferritin level got very low.
    • Hello I'm happy to join, any help is greatly appreciated as it can be difficult by times for sure. Unfortunately, I have been told my doctor has definitely not been doing anything correctly and very backwards about Alot of things. I live in canada, and there are celiac support groups I have found but I am about 2 hours away from any. I live in a pretty rural area. Although,  I have still received some help from them , they prefer a diagnosis before helping out to much. My doctor has me on a waiting list to see a gastrointestinal specialist but whenever I called her office to inquire about an appointment time I was told there was a very long wait and that I was considered to be a non emergency. So I am waiting to get an appointment. I have seen a dermatoligist for some of my rashes and she said it was dermatitis and gave me different creams for them.  It is frustrating because I don't know how to go about getting a actual diagnosis besides this biopsy. I was told to request a different specialist, but supposedly there is a waiting period for most in our area. 
    • Thanks for all of the replies. I've just found out I'm not getting to see a dietician because of not having a definite diagnosis which is another blow. I've had loads of bloods done but they just say they're all normal. I did have low vitamin D and high parathyroid but it's sorted itself out after a course of high dose vitamin D and they're not checking it again for a year. No chance of getting referred to endocrinology, gastro won't do it and neither will my gp. I've tried giving up coffee and all fizzy juice and it hasn't made a difference. I'm exhausted and scared and still have no clue what to do next. My gp has zero experience dealing with this type of thing - last time I was there she said it could be because I've restricted my diet too much and I should eat more gluten-free replacement products - everything I've read online says this is the worst thing to do! I'm asking for a copy of the last blood results this week so I can go through them myself but other than that I'm pretty stuck. 
    • I really am iffy on talking about this side of my gluten issues, I think I am about to ruin my reputation on this forum coming about as some extreme crazy guy saying this but I wanted to get this off my chest and perhaps see if anyone else might share a similar trauma. I get emotional recalling it, this side of my reactions, as it is most ingrained and very traumatizing experience, and I am not proud of it as the mentality I have now disgust me but I am going to come out about it. One of the scariest things in this world is when your own mind turns against you, when you can not think about what you want to think about, when you can not do what you know you should be able to do. When I got glutened really bad these where things I felt with my own mind would start looping, and thoughts would not come together. I would loose comprehension, feel like I know I should be able to think about something but my mind was not working. The same thing looped over and over and over like a broken record, This led to anger, anxiety, depression, panic, top it off with loss of feeling in my hands and feet, and the pains in the gut......it was a nightmare. I would go as far as beating my head against walls and punching them out of frustration as to why my own body and mind where not working, I just wanted it to end the pain to stop. I still have scars on my fist from punching into a nail in a stud once and kept going.....I scared everyone and myself distanced my self from loved ones. And started running a bucket list accepting that I was going to die soon. Hell to this day parts of the brain damage seem to be permanent as I can no longer do computer programing or some forms of math, they just no longer make any sense or connect. Then we learned what was causing it, and once the symptoms started to fade, I would get very angry if someone in the shared house did something stupid and got me sick again. The fear of going back to that caused violent and drastic actions to get away from what was making me sick. The sheer fear of my own mind turning on me led me to drastic actions to prevent it, throwing everything away I thought could make me sick, making sure no one else used that kitchen, used freezer paper and gloves when fixing my foods and working in there. I really destroyed and burned all bridges I had then and alienated myself from others. In the end it motivated me to learn how to cook, to get and renovate my own apartment in a building downtown, and start a business to pay for my new diet, by selling safe food to others with this issues locally at farmer markets. But it changed me on a very deep level, that traumatic experience to this day I have a issue looking at others and dealing with other humans who eat that stuff.......the stuff that breaks my mind and body so horrifically. If I have to compare it to something its like watching aliens drinking antifreeze and eating poison.....it causes a subconscious level of disgust and slight envy. I really can not even look at the stuff without recall what it does and feeling a twitch. I know I am the alien here, but it feels vise versa, and I look down on the normal people as odd creatures.  I go to the store and find myself overly avoiding contamination, keeping stuff in my own bags, asking the cashier to scan and bag it as I pass it not letting it touch that flour I see on the belt. I am hyper sensitive to the stuff I know and that fear semi dominates my mind as crazy as it sounds.  I am recovering and am forcing myself to try to mingle with other humans overlooking that one thing, but that deep rooted trauma still flares up as a protective measure especially around foods.  I could talk on and on about the other side effects but this one is the hardest to talk about it, and I feel others might be able to relate to it.    
    • Time.  You need time to heal.  Yeah, I am like a broken record!  😄 So...Lycra is your best friend for now (that and old baggy sweats!).  Hang in there!  Hugs!     
  • Upcoming Events

  • Blog Entries

  • Recent Status Updates

  • Who's Online (See full list)

  • Member Statistics

    • Total Members
      61,648
    • Most Online
      3,093

    Newest Member
    Mileenabug
    Joined