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

Celiac Biopsy Results - Overlaps with Lymphomas?


FemmeK
Go to solution Solved by Scott Adams,

Recommended Posts

FemmeK Newbie

Good morning. I got my biopsy results back from endoscopy and colonscopy. I have been trying to get in touch with the doctor to get clarity on some of the phrases in the pathology report. It says probable celiac but I am nervous about some of this and wondered if any of you had this language in your celiac results. If so, were you also referred for more consideration of certain Lymphomas of the intestine such as MALT Lymphoma? Or did you have this language in your results with still a straight celiac diagnosis? Thanks so much! 

"...focal surface intraepithelial lymphocytosis. The lamina propria is expanded by lymphoplasmacytic and eosinophilic infiltrate. Scattered lymphoepithelial lesions are present."

These "Lesions" are what make me most nervous because when I Google it, all I see are articles about Lymphomas - often secondary to celiac. 


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



Celiac.com Sponsor (A8-M):



  • Solution
Scott Adams Grand Master

Here's a breakdown of the terms in the biopsy report:

  • Focal Surface Intraepithelial Lymphocytosis: This suggests an increased number of lymphocytes (a type of white blood cell) within the surface layer of the intestinal lining (epithelium) in certain areas of the biopsy sample. In celiac disease, intraepithelial lymphocytosis is often observed.
  • Lamina Propria Expansion: The lamina propria is a layer of connective tissue just beneath the intestinal epithelium. "Expanded by lymphoplasmacytic and eosinophilic infiltrate" suggests that there is an increased presence of lymphocytes and plasma cells, as well as eosinophils, in this tissue. This can be indicative of inflammation.
  • Scattered Lymphoepithelial Lesions: This term indicates the presence of certain cellular changes in the mucosal lining of the intestine. These changes can be associated with celiac disease.

Overall, the biopsy findings you provided appear to be consistent with features often seen in celiac disease, such as intraepithelial lymphocytosis, inflammation in the lamina propria, and lymphoepithelial lesions. However, a definitive diagnosis and appropriate treatment should be determined by a gastroenterologist or healthcare professional who can consider the entire clinical picture, including symptoms, blood test results (such as serology for celiac antibodies), and other relevant information. It's important for the individual to discuss these results with their healthcare provider to get a clear understanding of their condition and develop an appropriate management plan.

FemmeK Newbie
1 hour ago, Scott Adams said:

Here's a breakdown of the terms in the biopsy report:

  • Focal Surface Intraepithelial Lymphocytosis: This suggests an increased number of lymphocytes (a type of white blood cell) within the surface layer of the intestinal lining (epithelium) in certain areas of the biopsy sample. In celiac disease, intraepithelial lymphocytosis is often observed.
  • Lamina Propria Expansion: The lamina propria is a layer of connective tissue just beneath the intestinal epithelium. "Expanded by lymphoplasmacytic and eosinophilic infiltrate" suggests that there is an increased presence of lymphocytes and plasma cells, as well as eosinophils, in this tissue. This can be indicative of inflammation.
  • Scattered Lymphoepithelial Lesions: This term indicates the presence of certain cellular changes in the mucosal lining of the intestine. These changes can be associated with celiac disease.

Overall, the biopsy findings you provided appear to be consistent with features often seen in celiac disease, such as intraepithelial lymphocytosis, inflammation in the lamina propria, and lymphoepithelial lesions. However, a definitive diagnosis and appropriate treatment should be determined by a gastroenterologist or healthcare professional who can consider the entire clinical picture, including symptoms, blood test results (such as serology for celiac antibodies), and other relevant information. It's important for the individual to discuss these results with their healthcare provider to get a clear understanding of their condition and develop an appropriate management plan.

Thank you SO much, Scott! I so appreciate your time in explaining these items to me! This is very helpful. When I Google some of these things in isolation, the results are skewed toward Lymphoma though I realized that this is not the best way to insure that I know how to interpret. I appreciate your time here. 

Scott Adams Grand Master

This article has some detailed information on how to be 100% gluten-free, so it may be helpful:

 

 

FemmeK Newbie

Thank you!! This is great. 

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
  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    2. - Gigi2025 replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    3. - Rejoicephd replied to JulieRe's topic in Related Issues & Disorders
      7

      Oral thrush question

    4. - ElenaM posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      I think I am gluten intolerant

    5. - JulieRe replied to JulieRe's topic in Related Issues & Disorders
      7

      Oral thrush question


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,897
    • Most Online (within 30 mins)
      7,748

    Sgp
    Newest Member
    Sgp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      You state in an earlier post that you don't have celiac disease. Here in this post you state you will "be doing another test". What will this test be looking for? What kind of celiac disease testing have you had done? If you have used a Entero Labs it sounds like you have had stool testing done for celiac disease which is not widely accepted as a valid celiac disease diagnostic testing method. Have you had blood antibody testing for celiac disease done and do you realize that for antibody testing to be valid you must have been eating generous amounts of gluten for a period of weeks/months? 
    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • catsrlife
      Back at the end of July I got this rash on both of my forearms. It started on my right and continued to the left. It was on the top and side. The rash has bumps that would pop with clear liquid if scratched. They would almost crystalize and scab up. They reminded me of chicken pox. They would scab for weeks and not heal much at all except for the blood clotting. If the scab was scratched off, it would bleed and bleed until it scabbed up again. The skin has lost its pigment where the scabs are. I figured it was probably either the plant I had trimmed around the 15th or some reaction to the magnesium complex I was taking or an allergic reaction to the asthma meds I was on. I stopped the asthma meds and the magnesium. The rash seemed to get better but when I took the asthma meds it flared up again so I went to the urgent care as my doctor was unavailable. The UC doctor said it probably wasn't the meds and asked about my diet. I said I was strict keto. I usually am, but there is a story around this. I feel amazing on keto. When I eat sugar, wheat, and starchy veggies I feel horrible. Blood sugar goes up, IBS type symptoms, brain fog, etc. But I have a horrible addiction to carbs so I blow it sometimes and after Mom died in 2023, I fell off the wagon. No rashes, just weight gain. I finally went back on keto and then around that time had a piece of pizza (or so, it's hard to stop the carb rush.) So I was strict keto, off and on. She ignored that and prescribed some allergy meds. It didn't go away.  What was happening by then was that the rash was now on my upper elbows, both of them, on the back of my arms. It starts with a very itchy bump, spreads around it and sometimes just burns like crazy and other times just itches. Then it started on the sides of my knees on the oustide, a little bit down the sides of the calves. It's not as bad there as it is on my arms even though it comes and goes (and so does wheat in my diet.) I then got three tiny blisters on each hand, 3 on the insdie of my index finger on the right hand and 3 on the inside of middle finger of my left hand. There is still a little scab there even though it was two weeks ago. No more have appeared on the fingers. But right now the back of the arms above my elbows are starting to itch. At some point I started to think mites from the possum that was sneaking into our house but it's been 3 months and they would be dead already. It wouldn't be from humans because I don't go near any humans although I did take an Uber to the doctor and the bus back. Plus, it's symmetrical. It starts on one side and is almost identical on the other.  I did my DNA with Ancestry and MyHeritage. I don't have the HLA-DQ2 or HLA-DQ8. I do have HLA-DQ2.2. I took the blood test but it was negative. Then again, I don't eat wheat every day. I rarely eat it except for lately when I've been preparing for the blood test if I have to take it again. I don't like to. It makes my joints hurt, gives me brain fog, stomach problems, I sleep in the middle of the day, etc. I have a doctor appointment tomorrow. I hope that she will be more serious about this than the UC doctor was.  So I have no idea. With my luck they'll magically disappear before the doctor appointment. That's what happens with everything.
    • ElenaM
      Hello everyone. I am Elena and am 38 years old. I suspect I have a gluten intolerance even if my celiac panel is ok. I have the following symptoms : facial flushing, Red dots not bumps în face, bloating abdominal distension, hair loss, depression anxiety even with meds and even bipolar. Fatigue extreme to the point of not being able to work. All of these after I eat gluten. Could I have non celiac gluten sensitivity? Thanks anyone else with these symptoms?
×
×
  • 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.