Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Biospy Results


Guest DONNAJ

Recommended Posts

Guest DONNAJ

Hi

Haven't posted for a long time sorry.

My daughter has had ongoing health issues since birth (reflux and milk protein allergy) she is now 2 years old.

We tried wheat free for 4 months different child (in a great way) no more sleep issues, uncontrollable behaviour,tearing at clothes, screaming for hours on end, horrible poos etc etc.

We reintroduced wheat nearly 3 months ago and have yesterday had a gastroscopy done, can anyone tell me what "initial findings abnormal cells"means???

She has double dose of the celiac gene sorry can't tell you which one I don't have the paper work in front of me and is still on neocate. Blood tests all negative (except low iron)

I'd appreciate any help/suggestions

thanks

donna


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



Celiac.com Sponsor (A8-M):



Kailynsmom Apprentice

IF the dr said that initial findings were abnormal, most likely that means celiac disease. Anemia is also VERY common with celiac disease, because the body isn't absorbing the vitamins and minerals from food.

Have you continued with the gluten-free diet?

Guest DONNAJ

[Thanks for your response. Is there anything else that "abnormal" could mean besides celiacs.

Also no she's not wheat/gluten free and hasn't been for the last 3 months in preparation for this op.

CDFAMILY Rookie

Hi Donna,

I thought my info on what happened to my daughter on a very slim gluten challange might be helpful. This is an old 1982 article on children and ferritin. My daughter was 17 at the time of the challange. She had had a negative biopsy in October but has had many serious physical problems which all point to Celiac. Mostly she had constant uncontrollable gas and burping since infancy which was only given an IBS dx. In 2004 I started a mega vitamin program for family because of my B12 deficiency that I found thanks to the internet. We started taking 5000mcg of methylcobalamin sublingual with folic acid and B complex. This just about cured both our gas and burping problems but we still had the fatigue. (I think this also repaired both of our upper small intestines as although I had very positive tTG and EMA, my damage was minor and DD was not visible but we were both still very sick.

Below is an article and her test results which I think are a good example of skipping biopsy and using blood work.

Open Original Shared Link

Am J Clin Pathol. 1982 Jan;77(1):82-6.

Related Articles, Links

Serum ferritin levels in celiac disease.

Souroujon M, Ashkenazi A, Lupo M, Levin S, Hegesh E.

Of the various common assayed parameters of iron metabolism, serum ferritin levels are the most discriminatory in distinguishing between non-treated celiac disease and other gastrointestinal disorders in the pediatric age group. Patients on normal diets usually have very low ferritin levels that increase at an average rate of 1 microgram/1/month when placed on a gluten-free diet. When the patient returns to a normal diet, however, ferritin levels decrease rapidly at an average rate of about 4 microgram/1/month. There is a relationship between abnormal intestinal changes and low ferritin levels in celiac disease with improvement in both when the patient is on a gluten-free diet. It is suggested that serial blood ferritin evaluations together with the leukocyte migration inhibition factor production assay should eliminate the need for invasive intestinal biopsies for the confirmation and possible follow-up to response to treatment.

PMID: 7055099 [PubMed - indexed for MEDLINE]

DD on very little gluten but lots of vitamins- Tested May 05

TIBC 424 (RANGE 222-400)

IRON 77 (RANGE 50-212)

FERRITIN 21 (RANGE 10-291)

SATURATION Not Taken

DD ON NO VITAMINS AND A LITTLE MORE GLUTEN BUT NOT ALL THAT MUCH ( started challenge around October after neg biop)- tested February 06

TIBC 527 (RANGE 222-400)

IRON 22 (RANGE 50-212)

FERRITIN 5 (RANGE 10-291)***( When the patient returns to a normal diet, however, ferritin levels decrease rapidly at an average rate of about 4 microgram/1/month)

SATURATION 4 (RANGE 16-35)

DD GLUTEN FREE 3 MONTHS and mega vitamins tested June 06

TIBC NT

IRON 149 (RANGE 50-212)

FERRITIN 23 (RANGE 10-291)-23 is still considered too low in my humble opinion

SATURATION 37 HIGH (RANGE 16-35)

Hope this helps,

Celiac Mom

Also another possible celiac disease blood sign is low or low normal lymphocytes.

chrissy Collaborator

abnormal cells could mean a number of things. it could mean there are increased lymphocytes, like you would see with celiac. it could mean there are eosinophilic cells, like you would see with food allergies. it could also probably mean that there is damage. the microscopic findings on the cellular level are much more significant than the initial findings.

kimber Enthusiast

Hi

SORRY I can't be of any help, but your dd sounds just like my ds (but he'll be 3 in October)

We are seeing a new GI in a few weeks...and I plan to discuss testing

Is your dd underweight...my ped continues to dismiss celiac for my ds because he is small, but not underweight

of course I spend my day trying to get him to eat

Thanks for any info

abnormal cells could mean a number of things. it could mean there are increased lymphocytes, like you would see with celiac. it could mean there are eosinophilic cells, like you would see with food allergies. it could also probably mean that there is damage. the microscopic findings on the cellular level are much more significant than the initial findings.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,974
    • Most Online (within 30 mins)
      7,748

    Srwells
    Newest Member
    Srwells
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      It's possible he's in the early stages of celiac disease, and it has been caught before villi damage. The blood test results so far do indicate possible celiac disease, as well as his strong family history of celiac disease. If his symptoms get better on a gluten-free diet this would be another strong indication. Personally I think it's definitely better to proceed on the safe side and go gluten-free, rather than to risk severe villi damage and all that comes with it.
    • Dora77
      For some context: I have type 1 diabetes (T1D) (since 11 years) and celiac disease(since 4 years) For about a year now, I’ve been experiencing permanent floating and undigested stools. I’ve had a pancreas elastase test done. The first result was extremely low at 44, but a second test came back at 236. My doctor said that since one result is normal, it rules out pancreatic insufficiency because, according to them, elastase levels would always stay low if that were the issue. However, could the 236 have been a false result? My doctor also thinks I don’t have pancreatic insufficiency because I’m able to gain weight. I also get hgh injections as my bone age is younger than my real age, this also contributes to weight gain, so I dont know if weight gain can rule out malabsorption. But maybe if I had real malabsorption I wouldnt gain any weight even with hgh? For celiac, I’m on a gluten-free diet, but there might b small cross-contamination from things like pepper labeled as “may contain gluten.” or sausages which dont have gluten ingredient but say may contain. My doctor said that small amounts like this wouldn’t harm me and even mentioned that an occasional small exposure to gluten may not do much damage (which seems questionable since I thought even tiny amounts could be harmful). She also said that when Im older (Im m17) I could try eating small amounts of gluten and do antibody blood tests to see if I can tolerate small amounts or not. For reference, I’m asymptomatic when it comes to celiac, so I have no idea if I’ve been “glutened” or not. My first concerning celiac blood test was semi high IgA, then 3 months later we did a check up and my IgA was high so it was confirmed celiac. Since than I’ve had celiac antibody tests done yearly to see how my diet is going, and they’ve been negative, but I’ve heard those aren’t always reliable. I’ve never had a follow-up endoscopy to confirm healing. I also always kept eating „may contain gluten“ food. (I live in Germany so I dont know if „may contain gluten“ is as risky as in the usa but I suppose both are as risky) These stool issues started around the same time I was doing excessive heavy lifting at the gym. Could stress or lifting have triggered this, or is that less likely since the symptoms persist even after I stopped lifting? Occasionally, I’ll feel very mild stomach discomfort, but it’s rare and not severe. My doctor (also a dietist) said floating, undigested stools could still be “normal,” but that doesn’t seem realistic to me. Could this be impacting my vitamin or protein absorption? I also did a fructose intolerance breath test and had a high baseline of 20 ppm, but it never increased—only decreased over time. I fasted for 12 hours and didn’t eat fructose beforehand, but my stomach didn’t feel completely empty during the test. Could this mean the test was inaccurate? For lactose intolerance, I did the breath test but only fasted 10 hours and had eaten lactose prior because I wasn’t aware of the proper diet restrictions. My results were: 14, 12, 15, 25, 35, 40, 40 ppm—which would be considered positive. But given that I didn’t fast long enough or follow the right diet, could this result be unreliable? Has anyone else dealt with similar symptoms? What ended up being the cause for you? And sorry for the long text!
    • TerryinCO
      The Docs' and NP haven't committed to Celiac determination yet but say go gluten-free diet because...  And I have with improved physical results - feeling better; overall functions better, and more energy.  Still 10 pounds down in weight but I still have BMI of ~23.  It's been just over a month now gluten-free diet.  I'm fortunate I get along with diary/milk well and most other foods. I wanted ask about this site's sponsor, gliadin X.  If this is legit, seems like a good product to keep on hand. Though it says it's only a safety for incidental gluten contact - not a substitue for gluten-free diet. What's your input on this? This may be sensitive subject since they're a sponsor. I've used resources here and other sites for information, gluten-free food/product lists. So thank you for all that support. That's it for now - Stay warm...  -2F this morning in Colorado!
    • cristiana
      I did suffer with gastric symptoms before diagnosis, but got all sorts of weird and wacky symptoms after going gluten free.   Things got much better once my antibodies fell to normal levels, but it took years (please don't panic, many people's go to normal levels relatively quickly when following a gluten-free diet). Causes of the symptoms you mention that I also experienced were iron supplements, a temporary dairy intolerance (this is common in coeliacs and should pass when your gut heals properly), and eating oats, as mentioned above.  Other symptoms I got were musculoskeletal pain after diagnosis, but again, once my coeliac blood tests were normal, I had no more pain. I did notice patterns emerging in foods that I reacted to and learned to steer clear of them, then gradually reintroduced them when my gut healed, such as soya, pure oats and dairy products.    You might like to keep a food diary. Cristiana
    • Jy11
      Well the conflicting results continue as the biopsy has come back negative. 😵‍💫 Waiting to discuss further but I really don’t know what to think now? Eight biopsy’s were taken from duodenum which surely should be sufficient if it was coeliac? 
×
×
  • Create New...