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Biopsy Results


PixeI

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PixeI Newbie

So I had a blood test and this is what I got:

Tissue Transglutaminase Immunoglobulin A (IgA): 25 U/mL

Abnormal <=14 ... though when I talked to the Dr he said it's supposed to be 1.  He then told me I had celiac disease.  I told him I can't have celiac disease.  He said he would do an endoscopy and colonoscopy.

He has been on vacation forEVER and it now just dawned on me that I have the results, I just don't know what they  mean.


In the OR notes, it says: "The second and third parts of the duodenum looked normal; however, the first part of the duodenum had some bumpiness to it that could reflect celiac disease."

And here is the surgical pathology notes.  I see 'patchy villous blunting', 'attenuated surface epithelium' and 'intraepithelial lymphocytosis, in keeping with lymphocytic colitis'

....So does this mean I have lymphocytic colitis instead of celiac disease?  There is a note of 'celiac?' in the Clinical History section but ... that's because they don't have my clinical history.  Do they not know?  I thought this was the gold standard of diagnosis?  I have been waiting for a month to get an answer back..... I can't wait any more..........

Please help if you can. :(


------------

 

DIAGNOSIS 1. Terminal ileum biopsy; Small bowel mucosa, no diagnostic abnormality.

2, 4, 5. Ascending, transverse, descending colon biopsies: Colonic mucosa, attenuated surface epithelium, intraepithelial lymphocytosis, in keeping with lymphocytic colitis.

3. Hepatic flexure polyp: Tubular adenoma, negative for high-grade dysplasia.

6. Rectum polyp: Tubulovillous adenoma, negative for high-grade dysplasia.

7,8. Duodenum 2,3 part biopsies: Duodenal mucosa, no diagnostic abnormality.

9. Duodenal cap biopsy: Duodenal mucosa, patchy villous blunting, no increase in intraepithelial lymphocytes, see comment.

10. Gastric antrum biopsy: Gastric antral mucosa, mild chronic gastritis, no activity, negative for H. pylori and intestinal metaplasia.

11. Gastric antrum ulcer biopsy: Antral type mucosa, reactive gastropathy with erosion, negative for H. pylori, intestinal metaplasia and dysplasia.

12. Gastric body biopsy: Gastric oxyntic mucosa, no significant abnormality, negative for H. pylori and intestinal metaplasia.

13. GE junction biopsy: Gastric cardia type mucosa, mild foveolar hyperplasia, negative for intestinal metaplasia and dysplasia.

CLINICAL HISTORY ? micro/collag colitis, ?adenomas ? celiac ? H Pylori ? ulcer ? reflux


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trents Grand Master

It seems clear to me, both from the antibody blood test and from the endoscopy, that you have celiac disease and you may also have colitis. There is a statistically higher incidence of IBS and colitis among the celiac population than is found outside the celiac population.

Scott Adams Grand Master

I'm curious why you would say this to your doctor: "I told him I can't have celiac disease"? Both your test results that you've shared here, and your own doctor have indicated that you likely do have celiac disease.

PixeI Newbie
1 hour ago, Scott Adams said:

I'm curious why you would say this to your doctor: "I told him I can't have celiac disease"? Both your test results that you've shared here, and your own doctor have indicated that you likely do have celiac disease.

Hey, sorry!

The doctor caught me completely by surprise.  I was just going in for a colonoscopy to screen for cancer (it runs in my family) and I didn't know he did a ttg iga test at that point.  Just before I was about to get sedated for the colonoscopy (which didn't WORK, btw!  I was awake and lucid for the whole thing!) he goes 'Oh by the way, you have celiac disease."

I was taken aback and said "No I don't!  I can't have celiac!  All I eat is bread and pasta!"

He said "Well now we're also going to do an endoscopy to confirm.  Let's check to be sure."

Then he went on vacation for a month and a half.  So I've just been left with this partial information on my own and going bananas.  In the meantime I have continued to eat gluten.  I just want to know if I actually have it or not. :(

PixeI Newbie
2 hours ago, trents said:

It seems clear to me, both from the antibody blood test and from the endoscopy, that you have celiac disease and you may also have colitis. There is a statistically higher incidence of IBS and colitis among the celiac population than is found outside the celiac population.

Okay, thank you so much for looking.  I suppose I can throw all hope that I don't have celiac out the window now then and start focusing on going gluten free.  Much appreciated!

trents Grand Master

You have already had both kinds of diagnostic procedures done (antibody and scoping/biopsy) and there are no more diagnostic tools left to check for celiac disease. Everything points to the fact that you are a celiac. Any more holding out would amount to denial. Start the gluten-free diet. 

 

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    • disneyfamilyfive
      Thank you for the article Scott. It was very informative.  I didn’t realize I should have been eating a certain amount of gluten prior to the test.  I only eat bread maybe 1x a week, don’t eat cereal.  Pasta occasionally.  I’m sure there is gluten in nearly everything, so I’ve had gluten but no idea how much, but definitely not slices of bread. Not sure how much or how little that could affect my results.  My doctor didn’t mention anything about eating more gluten or eating bread. 
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      I am looking for words of encouragement because I have just had enough with this celiac diagnosis. I recently got diagnosed in October this year and its been hell let me tell you. Fist of all my doctor did not want to do the test saying that I was not Celiac because I did not have blood in my stool. Really??? I thankfully insisted that he do the blood work test just to make sure., since I was sick while in italy after eating both pasta and pizza and I knew something was wrong. I exhibited all the signs of gluten sensitivity, bloating and bad stomach pain which I never had ever after eating gluten.  After a week of waiting patiently for the test result it showed positive. I was both happy and floored at the same time. It has been an emotional roller coaster. Having to now work hard  to read labels constantly making sure they don't add gluten EVERYWHERE!! buying some comfort expensive gluten free foods to somehow make me feel like I am a normal person again. Hiring a dietician to put me on a diet to get my nutrients needed and to fix my villi that is destroyed. I feel sad, angry, depressed and why me?? is it an italian thing? I do not know. Anyways any feedback would be helpful. I am still extremely tired and have bowel symptoms and brain fog when do these go away?
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