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

Cracks In The Corners Of My Mouth


Guest Chrisbee

Recommended Posts

Guest Chrisbee

All my life I have had upset stomachs and the only way I could work was to have a bottle of Kaopectate, or later, when it came out, Immodium. Couldn't go out to eat unless I took Immodium first. I also have joint and muscle pain, but the thing I think that drives me craziest is the corners of my mouth. I have had cracks and blisters there and on the lower part of my face and my hands and feet for fifteen years. I've had different prescription creams which sometimes help, but as soon as I stop them, it comes right back. The bottom of my face is always red and either blistered or peeling and the corners of my mouth are cracked and scarred. I haven't been diagnosed, but I had my son in to see our new family practitioner and mentioned some of our symptoms to him. He thinks it my be Celiac disease and is sending my son to see a pediatric gastroenterologist. Has anyone had blisters on their face, hands or feet and the awful cracks in the corners of their mouth? I decided to go gluten-free a few weeks ago and my face has improved some, but Sunday morning I woke up with the cracks and blisters again. The only thing I did different was take an OTC decongestant which I'm wondering if it contained gluten (maltodextrin was listed as an ingredient). Can these blisters be a Celiac symptom? I also have them on my neck and up into my scalp.


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



Celiac.com Sponsor (A8-M):



Generic Apprentice

I used to get cracks at the corners of my mouth when I was a kid pre-diagnosis. My mom is a nurse and says that the cracks are due to a vitamin b deficency. When ever I got them she gave me vit. b and it cleared up.

Yes, vitamin deficencies go along with celiac.

CarlaB Enthusiast

I got the cracks, too. I also heard it was a vitamin deficiency.

Maltodextrin is fine. Even though it sounds like it, there's no malt in it.

Be sure that you don't go gluten-free prior to testing, it will affect the results. If you think the blisters are dh, then that can be tested by a biopsy of the skin near the blister.

chrissy Collaborator

it can be a vitamin deficiency and it can be a symptom of celiac---but it can also be an infection----and there is something else that can cause the cracks, also---but i can't remember what it is. i looked it up because one of my kids was having a problem with it. one of my twins still has cracks in the corner of her mouth when she is gluten free.

Suzie-GFfamily Apprentice

The cracks near the corner of your mouth could be angular cheilitis. Angular cheilitis is a symptom of celiac disease.

There is a good (but slightly old) article in the American Family Physician journal called "Detecting Celiac Disease in Your Patients" by Harold Pruessner, M.D.

See figure 6 for a picture of angular cheilitis:

Open Original Shared Link

Generic Apprentice

That is a really good article, one of the best I have seen. Even if it is almost 10 years old. That man really has a good insight.

Guest cassidy

I've heard it could be related to candida overgrowth. I had a problem with candida last year and the corners of my mouth were so sore it hurt to smile. Candida is a common problem with celiac because your intestinal bacteria gets out of balance and the nasty stuff can grow out of control. If you look it up and you have other candida symptoms, that may be something to look into.


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



Celiac.com Sponsor (A8-M):



confused Community Regular
The cracks near the corner of your mouth could be angular cheilitis. Angular cheilitis is a symptom of celiac disease.

There is a good (but slightly old) article in the American Family Physician journal called "Detecting Celiac Disease in Your Patients" by Harold Pruessner, M.D.

See figure 6 for a picture of angular cheilitis:

Open Original Shared Link

That picture looks exactly like the things my son gets on his mouth. And the arm looks like my arm when i eat gluten.

paula

Guest Chrisbee

That picture looks exactly like what I've got. I've also got the hyper-pigmentation, which doctors told me was melasma and I should stay out of the sun.

I'll tell you what, the more I read the angrier I get. I've been to more doctors through the years than I can count, and none have ever tested me, my children, my brother or my father for celiac and we all have the same types of symptoms. My dad now has adenocarcinoma which they think originated in the appendix. He's had at least five surgeries and been through chemo. From what I read, that possibly could be related to celiac disease. I told Mom to mention celiac to his cancer specialist, but she ignored me. He's always had problems with his digestion.

I had problems all my life with my stomach too, but my mom always thought it was just nerves. When my little brother was in grade school, he developed the same problem and she took him back and forth to the doctor and they told her had a parasite from the well water or else he had developed salmonella from eggs. The first time I went to the doctor for my stomach problems, I was given a prescription for an anti-depressant and sent to a psychiatrist. This was a military doctor. I did actually feel better and gained some weight, but I got tired of feeling medicated and went off the anti-depressants. I lost the weight and had stomach problems again. I went to another military doctor who told me I had a spastic colon and I needed to eat more fiber. I went back when I developed swollen lymph nodes and had test after test run. My doctor diagnosed me with lupus and never told me what to do or how to treat it. I just put up with the joint pain, rashes, and stomach problems for the next ten years. When I had had enough, I went to doctor after doctor and was "diagnosed" with rheumatoid arthritis, Adult ADD, depression, connective tissue disorder, fibromyalgia, excema, psoriasis, osteo arthritis, and IBS. I gave up. Each doctor had a different opinion and people started to think I was a hypochondriac, especially my family.

My kids have had similar symptoms and I have run them from doctor to doctor too. My daughter has been to Shriner's Hospital, Children's Hospital in St. Louis, and Carle Clinic in Champaign to different rheumatologists. The last one wanted to give her a dose of chemo to put her in remission, but thankfully, she went into remission on her own before they got her in to do it. Her fingers swell and she gets big blisters on the palms of her hands and soles of her feet. She also has had alopecia and lots of stomach problems.

We need a good doctor!!!!!

And now I'm off to buy some vitamins!

  • 5 years later...
Brenda Sue Newbie

Hi All, I've just recovered from Angular Chelitis and I highly recommend this since it only took a couple of days once I used these products for my situation to clear up. :D My doctor wrote me a script for (generic name) Iodoquinol and Hydrocortisone. If you don't want to do the doctor route you can buy Hydrocortisone Creame 1% and Miconazole Creme over the counter, mix small equal amounts together and apply to the corners of your mouth. Apply the cream 3 or so times per day. I would also wash the area each time before reapplying cream. Oh, and drink from a straw until the corners of your mouth heals. You can also put Vaseline on the corners of your mouth overnight if you are worried about drooling onto your wound. Good luck cuz this aint a pretty thing to deal with. ;)

kareng Grand Master

Just an FYI, the original posts are 5 years old. They are probably not on this forum anymore.

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. - nanny marley replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      45

      Supplements for those Diagnosed with Celiac Disease

    3. - par18 replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Is it gluten?

    4. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

    5. - par18 replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

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

    • Total Members
      133,340
    • Most Online (within 30 mins)
      7,748

    Abbyyoung417
    Newest Member
    Abbyyoung417
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • nanny marley
      I have had a long year of testing unfortunately still not diagnosed , although one thing they definitely agree I'm gluten intolerant, the thing for me I have severe back troubles they wouldnt perform the tests and I couldn't have a full MRI because I'm allergic to the solution , we tryed believe me  I tryed lol , another was to have another blood test after consuming gluten but it makes me so bad I tryed it for only a week, and because I have a trapped sciatic nerve when I get bad bowels it sets that off terribly so I just take it on myself now , I eat a gluten free diet , I'm the best I've ever been , and if I slip I know it so for me i have my own diagnosis  and I act accordingly, sometimes it's not so straight forward for some of us , for the first time in years I can plan to go out , and I have been absorbing my food better , running to the toilet has become occasionally now instead of all the time , i hope you find a solution 🤗
    • asaT
      I was undiagnosed for decades. My ferritin when checked in 2003 was 3. It never went above 10 in the next 20 years. I was just told to "take iron". I finally requested the TTgIgA test in 2023 when I was well and truly done with the chronic fatigue and feeling awful. My numbers were off the charts on the whole panel.  they offered me an endoscopic biopsy 3 months later, but that i would need to continue eating gluten for it to be accurate. so i quit eating gluten and my intestine had healed by the time i had the biopsy (i'm guessing??). Why else would my TTgIgA be so high if not celiacs? Anyway, your ferritin will rise as your intestine heals and take HEME iron (brand 4 arrows). I took 20mg of this with vitamin c and lactoferrin and my ferritin went up, now sits around 35.  you will feel dramatically better getting your ferritin up, and you can do it orally with the right supplements. I wouldn't get an infusion, you will get as good or better results taking heme iron/vc/lf.  
    • par18
      Scott, I agree with everything you said except the term "false negative". It should be a "true negative" just plain negative. I actually looked up true/false negative/positive as it pertains to testing. The term "false negative" would be correct if you are positive (have anti-bodies) and the test did not pick them up. That would be a problem with the "test" itself. If you were gluten-free and got tested, you more than likely would test "true" negative or just negative. This means that the gluten-free diet is working and no anti-bodies should be present. I know it sounds confusing and if you don't agree feel free to respond. 
    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
    • par18
      Been off this forum for years. Is it that important that you get an official diagnosis of something? It appears like you had a trigger (wheat, gluten, whatever) and removing it has resolved your symptom. I can't speak for you, but I had known what my trigger was (gluten) years before my diagnosis I would just stay gluten-free and get on with my symptom free condition. I was diagnosed over 20 years ago and have been symptom free only excluding wheat, rye and barley. I tolerate all naturally gluten free whole foods including things like beans which actually helps to form the stools. 
×
×
  • 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.