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Possible Rash From Gluten? (Pic Heavy)


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43 replies to this topic

#1 SPJ&E

 
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Posted 20 April 2012 - 03:09 PM

I was directed here by another member, so hopefully you guys can help me out. My son is 7 months old and has had this rash off and on since he was 2 months old. Out of the last 5 months, I would say he has had clear skin for maybe 3 weeks total (all broken up). It is red, bumpy, and really itchy. He is totally miserable sometimes.

He was breastfed until 3.5 months (though I had to cut out 100% of dairy). I don't know if gluten goes through that or not?? But he has been on formula since then (Neocate). He has been getting solids since 5 months. He started out with oatmeal. We figured out the detergent allergy finally (all his skin can handle is Ecos F&C), but then the rash came back. It seemed to be about the same time he started getting more oatmeal (mainly to thicken the thinner baby foods) and Cheerios.

This rash has come and gone at what seems like random. His skin will clear up and look great for a week and then spots start appearing again. If it's a contact rash and we bathe him as soon as we notice, it goes away quickly (as with the detergent). This does not go away no matter how much we bathe him. We use hypoallergenic/unscented Dove on him and hypoallergenic/unscented Eucerin. His skin is not dry, just covered in itchy red bumps. It is usually the worst on his legs (thighs), though it varies. Sometimes it is from head-to-toe, sometimes just his arms and legs, sometimes legs and back and belly, etc. It is just completely random and we are at a loss.

His doctor is stumped by it and the dermatologist we seen was absolutely useless. I've never mentioned celiac to his doctor, but my mom was diagnosed with it about a year ago. For now, we have stopped giving him oatmeal and Cheerios and are just doing fruits & veggies, along with his formula just to see if it makes any difference.

Please ask any questions you might have. I tried to be thorough, but probably missed something important. Any advice is greatly appreciated...even if you could just point me in the right direction or tell me it looks nothing like a rash from gluten/celiac.

Here are some pictures from January and February. This is what his skin looks like at least 95% of the time.

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#2 squirmingitch

 
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Posted 20 April 2012 - 05:00 PM

O-M-G! OMG, OMG, OMG, OMG!!!!!!!!! Looking at those pictures (which are fabulous BTW; b/c they show it in such detail) are giving me flashbacks. The photos plus the fact that your mom was diagnosed with celiac ...... that poor baby has dh! And therefore celiac.

He must be miserable. I KNOW. He is miserable.

Okay, you need to get him tested right away. The sooner the better so you can get it done & get him started being gluten free. He can't go gluten-free until the testing is done but you will want the diagnosis for his benefit for the rest of his life you see. You need to see if you can find a GOOD derm who is EXPERIENCED in dh biopsy. And you need a pediatric gastro who is experienced in celiac diagnosis. I don't care where you have to drive to but you need to do it NOW. Talk to your mom's doc who diagnosed her & see if he/she can recommend the proper docs. OR take your son to your mom's doc & see what that doc says.

Meanwhile, use the coolest water he can stand to bathe in as hot water makes the dh even redder & itchier. Use witch hazel & soak cloths with it & swab him down --- it will help to cool the dh & help some with the itching. For that matter; after a bath you can just pour it on him. Since he seems to have allergies you will want to test the witch hazel first to make sure he's not allergic. I have a friend allergic to witch hazel so it does happen.

Get gluten-free everything you use on him --- shampoos, soaps, lotions --- everything.

I'm positive others will be on here to answer soon as well.

I'm crying for your poor baby. And that doesn't mean I think you're a bad parent. please understand I'm not knocking you in any way, shape or form. I just know the misery he's going through.
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Self diagnosed dh Sept. 2011~~~ confirmed dx July 18, 2012
Gluten free Dec. 2011
Soy free Dec. 2011
Hubs self diagnosed dh March 30, 2012
Hubs gluten free March 30, 2012

Summer 2013 We both have added back a little soy which is near unavoidable & we are doing okay with that small amount.

 


#3 squirmingitch

 
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Posted 20 April 2012 - 05:02 PM

Oh, and take those photos with you to any doc you go to.
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Self diagnosed dh Sept. 2011~~~ confirmed dx July 18, 2012
Gluten free Dec. 2011
Soy free Dec. 2011
Hubs self diagnosed dh March 30, 2012
Hubs gluten free March 30, 2012

Summer 2013 We both have added back a little soy which is near unavoidable & we are doing okay with that small amount.

 


#4 SPJ&E

 
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Posted 20 April 2012 - 05:33 PM

Thanks for your reply! I don't take anything you said as knocking me. I just want help! It's hard to see him digging at his arms and legs and knowing that I don't know what to do for him.

To respond to you though, we already drive about 1.5 hours to get to his ped because she is just wonderful, so it's not a big deal for us to drive to see other doctors for him. We actually prefer it, as quite honestly our local doctors suck. The dermatologist we seen was local and that was a waste of time. We have no problem going to another one, but it will definitely be one in a bigger city (we live in a very small town). His doctor wants to see him to discuss allergies, since it keeps coming back. So we will get that set up and go from there. She has always been great about listening to us and working with us on things.

The only problem with testing him is he has been on Prednisone off and on for about a month. He has been getting 1/4 tsp when it flares up really bad for days, he is miserable, and nothing is helping. He just had a dose this afternoon (and he looks muuuuch better). I know steroids can cause negative results on celiac tests. I think I read you are supposed to be steroid free for 1 month before testing? I'm sure she would have no problem testing him, but I don't want to put him through that if the steroid is going to interfere with the results anyway.
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#5 Momma4

 
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Posted 20 April 2012 - 05:50 PM

Poor thing! I totally feel for you! My 2 year old has rashes that start out looking like this but then he scratches so much they go a deep red color. His also comes and goes, but never seems to go totally away. I am no expert on this, as I just posted the same question a few days ago about my son, with pictures. However, I will say that your sons rash looks more severe and covers more of his body than my sons. I hope you get some answers soon!
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#6 rosetapper23

 
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Posted 20 April 2012 - 05:57 PM

I, too, think that your son has DH--it sure looks like it! If you can't find a dermatologist who is experienced with biopsying DH (and even if they say they ARE), make sure that whoever you find to do the biopsy takes the biopsy from clear skin ADJACENT to a lesion. If a biopsy is taken from a lesion itself, it will result in a negative pathology. This is VERY important, and very few dermatologists know this. If the biopsy is positive for DH, your son has celiac....and there's no reason for further labwork or an endoscopy. Many gastroenterologists are unaware of this and may insist on bloodwork and an endoscopy. There really is NO need to do so, since a diagnosis of DH is a diagnosis of celiac disease.

Have you checked to see if the formula is free of both gluten and iodine? It could be that it's fortified with iodine. If so, that's not good for your son. If he has DH and you eliminate only gluten at first, the iodine in his diet will keep the lesions active. You'll only need to eliminate the iodine for a month or two, and then you can add it back in slowly, since it's an important nutrient.

Please let us know what happens--I feel so sad looking at the photos you've taken.
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#7 pricklypear1971

 
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Posted 20 April 2012 - 05:57 PM

If you're looking for a good gluten-free cream try Vanicream.

No Aveeno!

If he will allow you, put some ice packs on the rash.

Yes, get the rash biopsied. It's your best bet, at his age, for a Celiac dx if indeed it is DH. Babies test neg most times on blood work and endoscope.

Poor little guy.

If you can't get a doc to biopsy it (and id get rather militant about it) you may try a gluten-free trial and see if it works.

Find a derm who is familiar with DH biopsies. It is worth it to find one who is experienced with it.
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Probable Endometriosis, in remission from childbirth since 2002.
Hashimoto's DX 2005.
Gluten-Free since 6/2011.
DH (and therefore Celiac) dx from ND
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Responsive to iodine withdrawal for DH (see quote, above).

Genetic tests reveal half DQ2, half DQ8 - I'm a weird bird!

#8 squirmingitch

 
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Posted 20 April 2012 - 06:13 PM

And tell the doctors that your mom was diagnosed with celiac.And for that matter you might ought to get tested yourself just so you know. It's harder to go back to gluten after you've gone gluten-free. Usually you have much stronger reactions going back on gluten for testing after having been gluten-free for a while.
And yes, the prednisone will invalidate any tests including the dh biopsy..
And the lab the doc sends the dh biopsy to can make all the difference in the world. They have to know they are supposed to look for dh. And I agree that the dh biopsy is the fastest & easiest way to get the diagnosis. And if a derm is unwilling to give the celiac dx upon a positive biopsy then see if your pediatrician will do so. But any derm worth their salt with dh is going to know a dh dx is a celiac dx.
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Self diagnosed dh Sept. 2011~~~ confirmed dx July 18, 2012
Gluten free Dec. 2011
Soy free Dec. 2011
Hubs self diagnosed dh March 30, 2012
Hubs gluten free March 30, 2012

Summer 2013 We both have added back a little soy which is near unavoidable & we are doing okay with that small amount.

 


#9 Di2011

 
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Posted 20 April 2012 - 11:35 PM

I think you're sons case would warrant a request for an immediate appointment. Insist on it.
It looks very much like my case (though I'm 39:) in its early days. I thought I was getting mosquito bites in the middle of a freezing winter. Now almost 12 months later my all over "bites" are finally beginning to heal. Hopefully given your sons age he may respond sooner than my 39 years of gluten-intake skin.

You may want to speak to your good doctor about antihistimine. It doesn't treat or cure or prevent but a good dose seems to take a little bit of the edge off especially during the horrible night time.

The only thing that has (literally) saved my sanity and allowed me patches of sleep are coldpacks (put in fridge as ice/freezer mightn't be so popular with a 2y/o). Buy the soft/material ones as these are much better. Have at least three so you can rotate them. Keep them clean (every use!!!) to prevent infection.
Some other things/advice:
* face clothes (wet and cooling on the skin) - perhaps use a soft cloth as most commercial face cloths tend to be a little abrasive
* soft cloth gloves (I still scratch like crazy but while I'm at home they are helpful. Perhaps you know someone who can sew?)
* keep his finger nails as short as you can and ALWAYS clean
* other people might disagree but you shouldn't have to use any soap everyday - consider giving him a totally chemical free day every other day or two
* don't use clothes washing powder. Buy a gluten free liquid.
* later down the track (post testing etc) you might have to consider making your entire household gluten free - it was only recently that I have done this and I am finally healing (with no change to my own diet or routines) and it has made an enormous difference.

I'll be thinking of you and bub the next few weeks. Keep us all update along the journey. And as suggested by others you MUST get tested. Celiac can come in a "silent" (but still potentially deadly) form also.
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#10 mushroom

 
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Posted 21 April 2012 - 02:43 AM

Yes, I am concerned about the prednisone interfering with his testing since it's goal is to reduce the inflammation you are tryhing to measure. I have read where you should be off it as long as you were on it (this was a five-month example) to get it out of your system. Now I know it is what gives him relief, but if you could eliminate the glluten and oatmeal, use the cold compresses, give him an antihistamine prescribed by his docor and have him wear the gloves, you might be able to keep him comfortable enough for a long enough time to get a valid biopsy. It is so tough to watch them suffer, but prednisone should not be a long-term treatment for a wee guy either.

I wish you well in your efforts to get him diagnosed and echo others who say it is really important to find a dermatologist who is familiar with celiac disease and its testing procedures.
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Self-diagnosed gluten intolerant, gluten-free Nov. 2007
Soy free March 2008
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Citric acid free June 2009
Potato starch free July 2009
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#11 squirmingitch

 
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Posted 21 April 2012 - 02:49 AM

According to these two sources; even for a dh biopsy you have to be eating gluten so he needs to be off the prednisone yet still eating gluten which is going to be hell b/c there is a rebound effect when going off the steroids. But better done now rather than later in life.

http://en.wikipedia....s_herpetiformis


http://www.coeliac.o...s-herpetiformis
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Self diagnosed dh Sept. 2011~~~ confirmed dx July 18, 2012
Gluten free Dec. 2011
Soy free Dec. 2011
Hubs self diagnosed dh March 30, 2012
Hubs gluten free March 30, 2012

Summer 2013 We both have added back a little soy which is near unavoidable & we are doing okay with that small amount.

 


#12 ciamarie

 
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Posted 21 April 2012 - 10:20 AM

My first thought on seeing the pictures was agreement with the others. Given all of the other great responses, it may be that testing asap would be your only option; knowing the results may be negative due to the steroids. OR, the best option might be to see if the ped dr. will diagnose based on family history, and those pictures after a gluten-free trial? If the gluten-free trial helps (which it undoubtedly would), you'd have before & after pics as well as family history and perhaps a genetic test? Obviously you'd want to check with the Dr. first, before taking that option. Then you could get him off gluten sooner, and have a dx.
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Gluten-free since the end of October 2011

#13 squirmingitch

 
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Posted 21 April 2012 - 11:59 AM

ciamarie brings up a good option. If you can get the ped to agree then it would be the fastest means to an end.
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Self diagnosed dh Sept. 2011~~~ confirmed dx July 18, 2012
Gluten free Dec. 2011
Soy free Dec. 2011
Hubs self diagnosed dh March 30, 2012
Hubs gluten free March 30, 2012

Summer 2013 We both have added back a little soy which is near unavoidable & we are doing okay with that small amount.

 


#14 JustNana

 
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Posted 21 April 2012 - 06:36 PM

Oh my Lord,

Your little guy's photos are heartbreaking. You did a great job by the way on the pics. I agree with all the posters here and know you want an answer. If it were my baby and I knew about DH I would go gluten free right away and see if a couple of months gives him any relief. He's only 7 months so feeding him is easy to control. I would not use any commercial baby foods. A little of your own soft cooked fruit and veggies for a while would be fine I think. Lots of babies are on just milk for 9-12 months and do fine. I feel so bad for you. I know that, miserable as he is, you are even more so.

Either way, staying on gluten, cutting the steroids and then testing... Or just doing a trial gluten free is at least something you can do. I know you feel helpless. You're not. Be firm with Drs if you are getting no answers.

I will keep your family in my prayers. Please keep us posted and know that you have many, many people here who know a lot and are genuinely caring.

Best wishes.

Linda
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#15 SPJ&E

 
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Posted 22 April 2012 - 03:42 AM

Thank you all for your responses! I can't tell you how much I appreciate any little bit of help/advice!! I am a bit overwhelmed, but definitely taking it all in. I sent an e-mail to his doctor and I'm sure she'll get back to me on Monday and we'll go from there. For now, we are just going gluten free, mainly because I can't make myself give it to him, thinking that might be causing that rash. He is out of the steroid, so we won't do anymore of that. The dermatologist just gave him enough for a few doses anyway. He does have a steroid cream, but again, we just won't use it.

I am thinking about having my 7 year old tested in the meantime. I've thought for a while, that he might have it, though I'm not sure. He has random bouts of diarrhea and tummy aches and has for years. He will eat and then all of the sudden have to run to the bathroom. Sometimes it's not diarrhea, but he has to go right that minute. I've started paying more attention to it lately and pasta does it everytime and sandwiches usually do as well. Before we thought it was the tomato sauce with the pasta (he also gets a rash around his mouth at times), but now I'm thinking it's the pasta. The other day we had bowtie pasta and sauce and afterward, he had diarrhea 3 times (it might have been 4). He hasn't been on a steroid and is still on gluten, so I thought testing him would be a good start.
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