Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Does This Sound Like The Right Testing For Dh?


climbmtwhitney

Recommended Posts

climbmtwhitney Apprentice

Hi All,

My already gluten-free DS has been getting awful rashes on elbows, back of neck, sometimes above knees too. They're very infrequent--about every few months sometimes six months or longer. Perhaps when he is being accidentally glutened. I have Celiac and my son is gluten intolerant. So, I'm wondering if he is actually Celiac as well and getting DH. From my research the rashes resemble DH in every respect. Took him to an allergist and did full skin testing. Nothing turned up. She suggested a dermatologist to look for DH or something else. Did that. He said he would do 2 biopsies on the next rash. The 1st to look under a microscope and see if the visual is consistent with DH. Then, if so, do a 2nd biopsy to check for the antibodies. Well, we did the 1st biopsy and just got the results. The visual looks like eczema. So no 2nd biopsy. Since when is eczema super infrequent and painful (brings him to tears)? Hmmm.

My questions....Can you tell if something is DH with a visual only? Or do we need a new doctor and a antibody biopsy? Has anyone else had a doctor insist on a visual look only first?

I'd really appreciate some insight. Thanks!!!

Jillian


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



mushroom Proficient

I have never heard of a procedure to look at the lesion itself. Common practice is to look for the antibodies in the skin adjacent to the lesion. Of course, some doctors don't know this and biopsy the lesion itself thinking this is the way to do it :P As for doing both, this is the first I ever heard of it. Jestgar might know if there are any changes observable in the skin itself that indicate DH, but it would sure be news to me. If there were, why do the other biopsy?

RoseTapper Newbie

I recently read on another thread that DH is a form of eczema.....maybe you should research that angle and challenge your doctor. To properly diagnose DH, the test DOES involve testing skin NEXT to the lesion. If the dermatologist doesn't know this, he needs to be informed (there's adequate literature on this that you can show him).

ChemistMama Contributor

I recently read on another thread that DH is a form of eczema.....maybe you should research that angle and challenge your doctor. To properly diagnose DH, the test DOES involve testing skin NEXT to the lesion. If the dermatologist doesn't know this, he needs to be informed (there's adequate literature on this that you can show him).

DH is similar to excema, but in the case of DH we actually know what causes it and what part of the immune system is involved. Not only does your Dr. need to biopsy next to the lesion, he has to do a direct immunofluorecence assay, which not many labs do. HEre is a link to print and show the doctor. Do not put your son on a gluten-free diet until he is properly diagnosed.

Open Original Shared Link

Here's a link to a lab who says they do this type of assay:

Open Original Shared Link

climbmtwhitney Apprentice

Thanks for the replies! Appreciate it!

My son is already gluten free. Has been for almost 2 years because he's gluten intolerant. But, now we think he might be Celiac like myself and my dd. The rash is very infrequent, but very severe. So, we (and his allergist) are thinking it's when he's glutened by mistake. I found a new dermatologist and registered my son. Now I just need to (gulp.) induce gluten and see if the rash appears. If so, I know we have our answer even without the test. But, I will go ahead and get another biopsy for a written diagnosis.

The first dermatologist makes me furious! :angry: Super arrogant. Usually the arrogant ones are the ones who haven't a clue what they're talking about. Figures. <_< Seems most everyone here in northern California uses UCSF lab for this stuff. Hopefully they can run the immunofluorecence assay properly. I knew we needed that. I just wanted to double check before I put my son thru another biopsy. He showed everyone at school his stitches. Poor little guy.

Thanks so much for the links. They actually mention how far away the skin sample needs to be from the lesions. So helpful!

Jillian

ChemistMama Contributor

Thanks for the replies! Appreciate it!

My son is already gluten free. Has been for almost 2 years because he's gluten intolerant. But, now we think he might be Celiac like myself and my dd. The rash is very infrequent, but very severe. So, we (and his allergist) are thinking it's when he's glutened by mistake. I found a new dermatologist and registered my son. Now I just need to (gulp.) induce gluten and see if the rash appears. If so, I know we have our answer even without the test. But, I will go ahead and get another biopsy for a written diagnosis.

Jillian-

After being gluten-free two years, the fluorecence test probably won't be useful, I'm afraid! After 2 years there isn't enough gluten built up in his skin, and unless it's a very new lesion, I have a feeling the test will come back negative. To get enough gluten, you'd have to have him eat gluten for about 4 weeks (!). This is what happenned to me, I was only gluten-free two months and the test was negative (done properly). He talked to someone in Dr. Fasano's Celiac clinic (U Maryland)and they said challenge 4-6 weeks. I didn't make it one day the pain was so bad.

If he's glutened by mistake, and you see lesions, you may want to try the iodine patch test, search the boards and you'll find it. Place a bandaid with the pad soaked in topical iodine near an active lesion. Leave it there as long as he can stand it, or 24 hours. If he has celiac the place where the patch is will be red and irritated and may even blister. That's proof he does have DH. HOwever, unless there's gluten in his system it won't work, and an accidental glutening may not even be enough, but it's something to try.

climbmtwhitney Apprentice

Jillian-

After being gluten-free two years, the fluorecence test probably won't be useful, I'm afraid! After 2 years there isn't enough gluten built up in his skin, and unless it's a very new lesion, I have a feeling the test will come back negative. To get enough gluten, you'd have to have him eat gluten for about 4 weeks (!). This is what happenned to me, I was only gluten-free two months and the test was negative (done properly). He talked to someone in Dr. Fasano's Celiac clinic (U Maryland)and they said challenge 4-6 weeks. I didn't make it one day the pain was so bad.

If he's glutened by mistake, and you see lesions, you may want to try the iodine patch test, search the boards and you'll find it. Place a bandaid with the pad soaked in topical iodine near an active lesion. Leave it there as long as he can stand it, or 24 hours. If he has celiac the place where the patch is will be red and irritated and may even blister. That's proof he does have DH. HOwever, unless there's gluten in his system it won't work, and an accidental glutening may not even be enough, but it's something to try.

ChemistMama,

Oh, I was afraid of that! I searched everywhere to try and figure out if you will still test positive after you've been gluten-free for awhile. Darn. We are still going to induce gluten next Sunday. We've got a week that's not too crazy so he won't be missing anything if he's miserable. I really hate doing it, but I'm quite sure it's the cause of his rash and we want an answer. We know that if he breaks out in the rash, it's Celiac, regardless of what the biopsy shows. He's already been extensively tested by his allergist, he has the genes, and tested as gluten intolerant. He also gets bad headaches and leg pains from gluten. Yep, feeling guilty already, but it's important to know. Thanks again for the help!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    2. - Scatterbrain replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    3. - knitty kitty replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    4. - knitty kitty replied to Larzipan's topic in Related Issues & Disorders
      34

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,314
    • Most Online (within 30 mins)
      7,748

    Lisa Gassick
    Newest Member
    Lisa Gassick
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Check your multivitamin to see if it contains Thiamine Mononitrate, which is a "shelf-stable" form of thiamine that doesn't break down with exposure to light, heat, and time sitting on a shelf waiting to be sold.  Our bodies have difficulty absorbing and utilizing it.  Only 30% is absorbed and less can be utilized.   There's some question as to how well multivitamins dissolve in the digestive tract.  You can test this at home.  YouTube has instructional videos.   Talk to your nutritionist about adding a B Complex.  The B vitamins are water soluble, so any excess is easily excreted if not needed.  Consider adding additional Thiamine in the forms Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) or thiamine hydrochloride.   Thiamine is needed to help control electrolytes.  Without sufficient thiamine, the kidneys loose electrolytes easily resulting in low sodium and chloride.   We need extra thiamine when we're emotionally stressed, physically ill, and when we exercise regularly, are an athlete, or do physical labor outdoors, and in hot weather.  Your return to activities and athletics may have depleted your thiamine and other B vitamins to a point symptoms are appearing.   The deficiency symptoms of B vitamins overlap, and can be pretty vague, or easily written off as due to something else like being tired after a busy day.  The symptoms you listed are the same as early B vitamin deficiency symptoms, especially Thiamine.  Thiamine deficiency symptoms can appear in as little as three days.  I recognize the symptoms as those I had when I was deficient.  It can get much worse. "My symptoms are as follows: Dizziness, lightheaded, headaches (mostly sinus), jaw/neck pain, severe tinnitus, joint stiffness, fatigue, irregular heart rate, post exercise muscle fatigue and soreness, brain fog, insomnia.  Generally feeling unwell." I took a B 50 Complex twice a day and extra thiamine in the forms Benfotiamine and TTFD.  I currently take the Ex Plus supplement used in this study which shows B vitamins, especially Thiamine B 1, Riboflavin B2, Pyridoxine B 6, and B12 Cobalamine are very helpful.   A functional evaluation of anti-fatigue and exercise performance improvement following vitamin B complex supplementation in healthy humans, a randomized double-blind trial https://pmc.ncbi.nlm.nih.gov/articles/PMC10542023/
    • Scatterbrain
      I am taking a multivitamin which is pretty bolstered with B’s.  Additional Calcium, D3, Magnesium, Vit C, and Ubiquinol.  Started Creapure creatine monohydrate in June for athletic recovery and brain fog.  I have been working with a Nutritionist along side my Dr. since February.  My TTG IGA levels in January were 52.8 and my DGP IGA was >250 (I don’t know the exact number since it was so high).  All my other labs were normal except Sodium and Chloride which were low.  I have more labs coming up in Dec.  I make my own bread, and don’t eat a lot of processed gluten-free snacks.
    • knitty kitty
      @Scatterbrain, What supplements are you taking? I agree that the problem may be nutritional deficiencies.  It's worth talking to a dietician or nutritionist about.   Did you get a Marsh score at your diagnosis?  Was your tTg IgA level very high?  These can indicate more intestinal damage and poorer absorption of nutrients.   Are you eating processed gluten free food stuffs?  Have you looked into the Autoimmune Protocol Diet?  
    • knitty kitty
      Vitamin and mineral deficiencies can make TMJ worse.  Vitamins like B12 , Thiamine B1, and Pyridoxine B6 help relieve pain.  Half of the patients in one study were deficient in these three vitamins in one study below. Malabsorption of vitamins and minerals is common in celiac disease.  It's important to eat healthy nutrient dense diets like the Autoimmune Protocol Diet, a Paleo diet that has similarities to the Mediterranean diet mentioned in one of the studies.   Is there a link between diet and painful temporomandibular disorders? A cross-sectional study https://pmc.ncbi.nlm.nih.gov/articles/PMC12442269/   Nutritional Strategies for Chronic Craniofacial Pain and Temporomandibular Disorders: Current Clinical and Preclinical Insights https://pmc.ncbi.nlm.nih.gov/articles/PMC11397166/   Serum nutrient deficiencies in the patient with complex temporomandibular joint problems https://pmc.ncbi.nlm.nih.gov/articles/PMC2446412/  
    • Iam
      Yes.  I have had the tmj condition for 40 years. My only help was strictly following celiac and also eliminating soy.  Numerous dental visits and several professionally made bite plates  did very little to help with symptoms
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.