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

Enlarged Spleen


alevoy18

Recommended Posts

alevoy18 Explorer

Hi Everyone,

I was diagnosed by tTG blood test and positive biopsy (Marsh 3B) in November 2009. Over the last couple of years I've had a few ultrasounds, due to finding lymph nodes in my neck/armpit. Prediagnosis I had a Ultrasound that showed my spleen as 11cm long. 6 months later after going gluten free, I had another ultrasound which showed my spleen was still normal sized at 10.6cm long. On my most recent U/S (Feb 2), my spleen was 14cm long and listed as mild/moderate splenomagly.

Has anyone experienced this? I have had issues with my RBC/HB/HCT counts being borderline low for the last couple of years and my reticulocyte (immature red blood cells) counts being extremely low. I saw a hematologist, but they were not concerned until my red cells dropped lower. I'm just curious if anyone knows what the enlarged spleen is likely from or if I should see my doctor about it. A specialist ordered the U/S for the lymph nodes, no nodes were found in the abdominal section, just the spleen size. Is the spleen something that needs to be investigated or do I not need to bring it up to my family doctor?

As for the lymph nodes, last check the largest in my neck was 2.0cm x 0.8cm and the largest in my right armpit is 3cm x 1.5cm. The biopsy of the armpit had a damaged specimen, so I am awaiting to see if I need another one. This is all likely nothing since my CBC tests are only borderline low, but I would like a bone marrow biopsy to ease my mind. Does anybody agree with the biopsy being done or am I just worrying too much?

Thanks a lot!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

If your doctors are not concerned you should try not to be either. Many things can cause enlarged lymph nodes and not all are dire. The inflammation from celiac can do it and it does take a very, very long time for them to go down. The spleen is I think a sort of filter and if the amount of increase was something to worry about the doctor should let you know. If you are really concerned make an appointment with your doctor to discuss it.

Looking for answers Contributor

I have enlarges lymph nodes in my neck that have been there for years. Most of my blood count comes back in on the low end as well, and sometimes low and out of range. I had a CT scan done on my neck for the lymph nodes, and results said they were not found to be malignant. For years I stirred about it, and sometime still do. However, I've seen several doctors and naturpaths that all say enlarged lymph nodes are completely "normal" for people with autoimmune issues and are nothing to be concerned about. So, basically, unless they suddenly balloon which would result in cause for concern, I just have to learn to live with them. :rolleyes:

SaraKat Contributor

I had enlarged axillary lymph nodes on the left side and that really scared me- that was before the celiac dx. I thought I had lymphoma. I guess it is from celiac, they have gone down, but they were a little over 2cm (there were 2 that were enlarged). I never had an issue with the spleen though.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    Carol Zimmer
    Newest Member
    Carol Zimmer
    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

    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
×
×
  • 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.