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

Biopsy Negative For Dh


kmag

Recommended Posts

kmag Rookie

Biopsy came back negative, which did not surprise me since every other celiac related test has come back negative. Apparantly, being itchy and having my guts in knots is perfectly normal.

He says there could be a false negative and prescribed me two months of Dapsone. The idea being if the rash goes away, it's positive for DH. If rash persists, it's not DH.

Dapsone scares me, frankly. I already have trouble keeping my iron up and am near the end of training for my first marathon. I don't need my hemoglobin being messed with right now (or ever, really).

I cut out gluten 8 weeks ago and have noticed an improvement in my skin. Still itchy but less intense and no longer burning/stinging. My belly is so much happier without gluten, too.

So, Dapsone or no Dapsone? I'd love to know definitively if it's DH, but I'm concerned about the potential cost to my health. Or should I just continue on with the gluten free diet and see what happens?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Have you eliminated iodine from your foods and supplements? We need to as iodine will keep the antibodies active. Personally I would do that first and also make sure that gluten ingredients are eliminated from all personal care products. It can take some time for the antibodies to leave the skin and even a tiny amount will reactivate them so do be very strict with the gluten avoidance.

eatmeat4good Enthusiast

Dapsone worked great...for two weeks.

Then I broke out all over head to toe with raised red pinpoint dots. So no Dapsone for me. You are right to be concerned. Make sure and do the blood tests if you do take it.

I was strictly gluten free for 4 months with minor healing...and flares. Only when i eliminated iodine strictly did I start to heal. It took three full months. I saw Endocrinologist today and asked him about limiting iodine since we need it in our body. He said that kind of temporary limiting...even for several months...would not be harmful as long as you add it back when you heal. So I feel good about what I did. I was concerned it might hurt the thyroid.

You are very active, so it might effect you more...limiting iodine. I know we need it. But you will have to figure out how long to avoid it for you. If you keep on eating iodized salt though, you may still have problems like Ravenwood said. Strict iodine and gluten avoidance will work, but any tiny accidental cross contamination or iodine intake will cause a reaction. At least it does for me. I pay for it for several weeks with sores.

Dapsone DID help the Dr. to believe I had DH. The pain and itching went away during the medication. But it wasn't really worth it to me...I already knew I had it. Hope you heal fast.

kmag Rookie

I had read about the iodine connection here, but kind of dismissed it. I'm having more trouble wrapping my brain around no dairy and eggs than I did about removing gluten from my diet. I never put salt on my food, and mainly eat whole foods, but seriously, the dairy and eggs will be hard to give up. I did notice that my iron supplement has iodine in it, too.

Does the salt listed in any processed food always mean iodised salt? I absolutely need salt as a runner, just not the iodine.

itchy Rookie

Kmag, my experience is somewhat different. I haven't used Dapsone or avoided iodine. My lesions are almost healed and don't sting or itch much any more. But it has been many months.

The advantage of doing it 'cold turkey' if you can is that you will become very aware of those 'marginal' foods that contain small but significant amounts of gluten.

You won't risk the side effects of Dapsone, or the health risks of a low iodine diet.

I think the choice of which strategy to follow depends a lot on your personal circumstances, how you assess risk and how much unpleasantness you are willing to tolerate. As well as your specific reactions which will vary from the rest of us.

Best wishes.

eatmeat4good Enthusiast

I wondered about processed foods having iodized salt. Sometimes I reacted to them. So I didn't eat them while I was trying to heal DH. I heard organic dairy doesn't contain as much iodine. Here is what I figured out about dairy and DH...If a product has carageenan in it, my DH reacts. Carageenan is made from seaweed and seaweed contains iodine. So organic that does not have carageenan should be ok if you can tolerate dairy. Eggs sometimes made me react, sometimes not.

You can use all the salt you want if you use uniodized salt. It is sold right next to the iodized salt. Sea salt made me react though and the article on DH here on this site says not to consume sea salt or seafood. Indeed, they both made me react with activated lesions until I realized that it really is true that the iodine needed to be limited or eliminated for a short time.

Shellfish is the worst for my DH. Oh my God. I think freshwater fish is supposed to be OK, but not seafood it you are trying to limit iodine.

It is a real puzzle figuring out what activates your DH. Asparagus also has a high iodine content.

I do think iodized salt is used in processed foods, like canned goods, because it is easily obtained.

Just start trying things and eliminating and most importantly be certain to eliminate all traces of gluten because it is awful for DH...even tiny CC can cause rash for weeks.

sb2178 Enthusiast

I think, in the US, that processed foods always have iodized salt. I vaguely think that's a federal reg, but could be wrong. Canning salt is always w/o iodine, and I believe some kosher salts also do not have iodine.

Fake milks aren't that bad for cooking, or on cereal.


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



Celiac.com Sponsor (A8-M):



relieved Newbie

Biopsy came back negative, which did not surprise me since every other celiac related test has come back negative. Apparantly, being itchy and having my guts in knots is perfectly normal.

He says there could be a false negative and prescribed me two months of Dapsone. The idea being if the rash goes away, it's positive for DH. If rash persists, it's not DH.

Dapsone scares me, frankly. I already have trouble keeping my iron up and am near the end of training for my first marathon. I don't need my hemoglobin being messed with right now (or ever, really).

I cut out gluten 8 weeks ago and have noticed an improvement in my skin. Still itchy but less intense and no longer burning/stinging. My belly is so much happier without gluten, too.

So, Dapsone or no Dapsone? I'd love to know definitively if it's DH, but I'm concerned about the potential cost to my health. Or should I just continue on with the gluten free diet and see what happens?

I have been gluten-free for 1 1/2 years and my DH is slowly going away. I am on 5 different creams to treat the rash. Dapsone is one of those creams. It really helps! Maybe you could try a cream instead of the pill? Just a thought.

kmag Rookie

Thank you for all your responses. There really is a wealth of information to be found here.

Almost 10 weeks gluten free, though the other day I made tuna salad for my son using a CC jar of Miracle Whip and licked the spoon afterward. Days later I am itchy as hell. Seriously, that minute amount can do that?

I was thinking I may try the Dapsone after the marathon is over and see what kind of response I get from it. If it clears the rash, then I know it's DH and I'll quit taking it and continue gluten free forever. The dermatologist did not care about doing regular blood work while on Dapsone, so I'll get my GP to do it. I work in a clinic so it's easy enough.

For anyone who has taken Dapsone, I'm curious how quickly it worked for you?

Hopeful1950 Explorer

Hi,

I tried Dapsone (25mg/day) and got relief from the intense itching of my rash in about three days and the sores started to heal because I wasn't scratching them. I was so excited! I was still getting a few new little blisters so the doc started gradually increasing the dose until I was up to 100mg per day. At that dose the rash was under control, but I developed bad side effects so discontinued the medication. When I discontinued, the rash came back with a vengeance. I think it would be okay to take it for a week or less as a diagnostic tool, but be prepared for a possible flare when you stop the med.

I have tried the topical Dapsone (Aczone)and it doesn't work for me. Very expensive.

eatmeat4good Enthusiast

I tried Dapsone for two weeks. The first week was great! Immediately stopped the stinging and burning rash...though the sores were still there. By the end of the second week I developed an all over body rash that was raised red bumps and it was awful and took 2 more weeks to go away. I immediately stopped the Dapsone. Ugh

Yes, that minute amount can "get" you. It gets me every time I make a mistake. Then the rash will flare for few weeks. Ugh.

Hopeful is right that the DH will flare on stopping Dapsone. It was really irritated.

Have you figured out if Iodine causes you to react? Did you eat any of the tuna? Tuna causes me a reaction every time...still....after 7 months gluten free. I think it is the iodine. But who knows. Please post anything you learn about controlling your rash...

kmag Rookie

It sounds like side effects are pretty common with this medication, unfortunately. Not really looking forward to a flare-up if it happens, but whatever.

Yes, I did eat some tuna with the mayo. I never do think about the iodine part of the equation, and so far haven't done anything to figure out if that aggravates the rash at all. I just keep hoping that not eating gluten will make it magically disappear.

The only I know about controlling the rash is if I don't scratch it's better. I'm sure you'll all find that very helpful - Haha :)

Hopeful1950 Explorer

Mayo bugs my rash because it is made with eggs which are high in iodine. If I ate tuna + mayo I would really blister!

rosetapper23 Explorer

For me, the equation was always that the iodine caused the DH to worsen even more than the gluten. Twelve years before I ever discovered I had celiac, I made the connection to iodine when it came to the itching blisters. I found out that if I avoided iodine entirely, I could control the rash. Of course, 12 years later, I discovered the true cause behind the blisters and have been rash-free ever since. Unfortunately, from avoiding iodine for 12 years, I ended up being hypothyroid....and the medication contains iodine. However, as long as I avoid gluten, the blisters haven't returned. I do, however, have a chronic rash across the upper part of my back, and I've been assured that I will have it for the rest of my life....all because of the iodine.

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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,915
    • Most Online (within 30 mins)
      7,748

    DRIZZE
    Newest Member
    DRIZZE
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.