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

Biopsy Results - Please Interpret If You Are Able!


Elisec5678

Recommended Posts

Elisec5678 Newbie

Hello!

I tested positive for Celiac Disease via a blood test almost 2 weeks ago. My Tissue Transglutaminase Antibody, IgA was 64 U/mL (standard range is 0.0 - 6.9 U/mL) and was interpreted as positive.

I just had an endoscopy about 5 days ago and just received the results. Can someone please help me interpret these, primarily the severity of celiac?

Here is exactly how they appear (everything in quotations):

 

"FINAL DIAGNOSIS

Duodenum, biopsy:

 - Villous atrophy, near total, and intraepithelial lymphocytosis consistent with celiac disease in the proper clinical setting

 

Clinical Information

TTG abnormal

 

Microscopic Description

Microscopic examination is performed.

 

Gross Description

A:

 - The specimen is received in formalin and labeled with the patient's name and "Duodenum".  The specimen consists of multiple tan-white irregular soft tissue fragments, averaging 0.2 cm. The specimen is filtered and entirely submitted in one cassette. AW"

 

Thank you!


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Elisec5678, welcome to the forum!

Yes, your tTG-IGA at 64 is clearly positive.

Concerning the biopsy report, celiac disease is an autoimmune disorder that causes inflammation in the lining of the small bowel when gluten is ingested. This lining consists of a landscape of tiny finger-like protrusions that create an extensive surface area for absorbing the nutrients from our food, such as vitamins and minerals. These projections are called "villi". In the celiac population, the constant inflammation from gluten ingestion causes damage to the villi, blunting or rounding them off such that we lose surface area for nutrient absorption. Thus, nutrient absorption becomes less and less efficient, resulting in various nutritional deficiency diseases, even though we may be eating well.

Your report indicates that you have suffered from undiagnosed celiac disease for a long time, such that your villous lining is almost completely destroyed. With diligence in gluten free eating it will likely be restored in around two years, depending on your age and other factors.

Is this helpful or do you have other questions?

yuluyouyue Contributor
27 minutes ago, Elisec5678 said:

Hello!

I tested positive for Celiac Disease via a blood test almost 2 weeks ago. My Tissue Transglutaminase Antibody, IgA was 64 U/mL (standard range is 0.0 - 6.9 U/mL) and was interpreted as positive.

I just had an endoscopy about 5 days ago and just received the results. Can someone please help me interpret these, primarily the severity of celiac?

Here is exactly how they appear (everything in quotations):

 

"FINAL DIAGNOSIS

Duodenum, biopsy:

 - Villous atrophy, near total, and intraepithelial lymphocytosis consistent with celiac disease in the proper clinical setting

 

Clinical Information

TTG abnormal

 

Microscopic Description

Microscopic examination is performed.

 

Gross Description

A:

 - The specimen is received in formalin and labeled with the patient's name and "Duodenum".  The specimen consists of multiple tan-white irregular soft tissue fragments, averaging 0.2 cm. The specimen is filtered and entirely submitted in one cassette. AW"

 

Thank you!

Hello. Almost the same description was on my biopsy report. Plus it also said it was Marsh 3 damage which is almost total damage. But don't let this discourage you. Your villi will heal on gluten free diet and then your starting point won't matter, ie. you will be no different than someone who had mild damage at diagnosis. 

Elisec5678 Newbie

Thank you both so much for your responses - both very helpful!! Much appreciated. 
 

Do these biopsy results mean I have to be more careful about cross contamination, etc. than others? Or anything else I should know about them?

Also, I have a very high PTH value and low bone density and I am 26 years old. Should I expect these to improve on gluten free diet?

Thanks again for the help!!

trents Grand Master

Bone remineralization should happen at your age I would think if you maintain a strict gluten-free diet. It would also be important in that regard for you to begin some serious vitamin and mineral supplementation. Make sure you purchase vitamin and mineral products that are certified gluten-free as wheat starch can be used as a filler in pills. Costco's Nature Made and Kirkland Signature brands are good choices and will state clearly on the label if they are gluten free. I would recommend adult multi vit (like Centrum), a high potency B-complex, 5000IU of D3 and either Magnesium citrate or Magnesium glycinate (these two forms are well-assimilated comparted to the less expensive and more common magnesium oxide). Start with a small dose and titrate up on the magnesium supplement until you reach the point where it is causing loose stools (think, "Milk of Magnesia) and then cut back a tad. Magnesium and D3 are very important to bone health. Don't worry about B-vitamin toxicity. They are water soluble and you will pee out any excess. I would avoid excessive calcium supplementation as it can change gut PH and be counter productive. Your problem isn't insufficient dietary calcium but rather poor assimilation because of villi blunting.

The biopsy results are not an indicator of how sensitive you are to gluten but rather how long you have been living with celiac disease. I cannot emphasize more strongly that you need to take CC (cross contamination seriously. That doesn't mean you have to become obsessive compulsive about it but it does mean you can't be lazy about it or take anything for granted. Don't necessarily rely on gut discomfort as an indicator of being "glutened". Small amounts of gluten can create inflammation in the small bowel lining that you are unaware of and sabotage healing.

Learning to eat gluten-free is more of a challenge than most people imagine at the outset. There is much to learn about how gluten is deployed and hidden in processed foods by the food industry (terminology) and then there is the whole issue of cross contamination. It's easy to eliminate the major sources of gluten in our lives but harder to eat truly gluten-free. Perhaps this will help you get started: 

It takes a year or two to get really savvy about avoiding gluten but with time you sort of develop a sixth sense about it.

Be aware also that the dairy protein casein can cause villi blunting in some celiacs just like gluten and many celiacs are also lactose intolerant. About 10% of celiacs react to the oat protein avenin like they do gluten. So if avoiding gluten doesn't relive your symptoms like you expect, look at these other things.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,977
    • Most Online (within 30 mins)
      7,748

    P Jackman
    Newest Member
    P Jackman
    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...