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

Lymph Nodes(?)


CatcherInTheRye

Recommended Posts

CatcherInTheRye Apprentice

As long as I can remember I have had an enlarged lymph node on the side of my neck, but in my teenage years I got a few more (one on the back of my head, one directly where my neck meets my head in the front). I suspect they were with me pre-celiac (can't be sure) but they've  kind off always been around. Most Drs seem disinterested in them and say its normal but sometimes I still get anxious about them. Does anyone have anything like this? How common is this? I am wondering if they are somehow tied to celiac. 


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



Celiac.com Sponsor (A8-M):



trents Grand Master

And you are sure these are swollen lymph nodes and not just some kind of cyst?

https://www.healthline.com/health/sebaceous-cyst

CatcherInTheRye Apprentice
1 minute ago, trents said:

And you are sure these are swollen lymph nodes and not just some kind of cyst?

https://www.healthline.com/health/sebaceous-cyst

Quite possible. Never been confirmed one way or the other and Drs usually don't correct me when I suggest they are lymph nodes

trents Grand Master

They may have chosen to just be polite. I do computer repair and technology support and realize I can't always correct my customer's misconceptions and misnomers. I generally know what they are trying to say even if they don't say it correctly and it's often easier just to fix the issue rather than to educate. Most likely, they won't remember it anyway and some people feel put down when you try to correct them, no matter how graciously you try to do it.

I had a sebaceous cyst removed from the back of my head some years ago because I was constantly injuring it when combing my hair.

There is also something called a lipoma which is a nodule under the skin filled with fatty material. I have a few of those in places that don't bother me.

Fenrir Community Regular

Chances are if you have lumps on your body for years and the Dr. isn't concerned they're probably not lymph nodes. Chronically swollen lymph nodes would be something every Dr. would be concerned with. 

Chances are you just have cysts or lipomas as stated above. 

I had a cyst removed from my head years ago, my mother had several of them. Drs generally wont recommend treatment or think anything of them unless they are unusually large or painful. 

knitty kitty Grand Master
On 2/19/2020 at 9:26 AM, CatcherInTheRye said:

As long as I can remember I have had an enlarged lymph node on the side of my neck, but in my teenage years I got a few more (one on the back of my head, one directly where my neck meets my head in the front). I suspect they were with me pre-celiac (can't be sure) but they've  kind off always been around. Most Drs seem disinterested in them and say its normal but sometimes I still get anxious about them. Does anyone have anything like this? How common is this? I am wondering if they are somehow tied to celiac. 

I've had a swollen gland in my neck similar to what you described.  I found that taking thiamine helps immensely.  

Here's an article that you might find helpful.....

http://wandererandhome.weebly.com/heal-yourself/vitamin-b1-thiamine

I had started taking more thiamine for my Type Two Diabetes, and my neck gland went away.  Later I found that article that explains why.

Hope this helps!

 

Julia rowlands Newbie
On ‎2‎/‎19‎/‎2020 at 3:26 PM, CatcherInTheRye said:

As long as I can remember I have had an enlarged lymph node on the side of my neck, but in my teenage years I got a few more (one on the back of my head, one directly where my neck meets my head in the front). I suspect they were with me pre-celiac (can't be sure) but they've  kind off always been around. Most Drs seem disinterested in them and say its normal but sometimes I still get anxious about them. Does anyone have anything like this? How common is this? I am wondering if they are somehow tied to celiac. 

I had swollen glands both sides under my jaw, size of golf balls, was eventually diagnosed celiac 3 years ago by scope and bloods, then 2 years later when antibodies reduced from 130 down to 22 proved gluten-free diet works, however repeat bloods first showed cholesterol high, reduce repeat bloods, 2nd bloods showed cholesterol now ok but diabetes high, reduce sugar and repeat, 3rd  bloods showed diabetes now ok but thyroid high, over active, investigative scan showed no nodules on throat but found out graves disease was causing the over active thyroid, lost 2 stone in weight I shld mention prior to diagnosis, consultant said wld take 18 months to control it, currently 12 months in on neomarcazole, graves is also autoimmune not mentioned in most common autoimmune lists, either genetic or extreme stress / trauma, its also a disease originated in Ireland, anyhow to get back to the glands, they are now back to normal .


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



Celiac.com Sponsor (A8-M):



trents Grand Master

It's good to hear things are more or less under control now. Sounds like quite a medical ordeal you have been through and a long winding rode. Thanks for sharing. So many more medical problems are autoimmune based than most people realize.

knitty kitty Grand Master

Thiamine deficiency is associated with diabetes and hyperthyroidism (as well as hypothyroidism) and high bad cholesterol levels.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921172/#!po=47.9167

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376872/#!po=1.02041

https://www.ncbi.nlm.nih.gov/pubmed/?term=Thyrotoxicosis+thiamine

https://jamanetwork.com/journals/jama/article-abstract/265475

Celiac Disease causes malabsorption which results in malnutrition.  It's hard to get well when you can't absorb vitamins and minerals through your injured intestines.  Consider supplementing until you heal. 

Been through all these illnesses with my own thiamine deficiency.  

Hope this helps.....

K

 

  • 9 months later...
CatcherInTheRye Apprentice

Scary stuff. Glad you are feeling better Julia. Thanks for all the replies everyone. I had thyroid tests on an unrelated issue and all seemed well. Might try thiamine but I may just be lumpy I'm afraid. 

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
      126,079
    • Most Online (within 30 mins)
      7,748

    Kassie S
    Newest Member
    Kassie S
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Could be the Ozampic is masking your expected symptoms.  Like an analgesic masks pain.  Qzampic slows digestion to lower the rate glucose enters the intestine to slow its effect on glucose level.  It seems it might also slow down the gluten entry into the intestine, reducing its trigger level for the antibodies.  Ultimately the damage from gluten is the same, just not as fast so the pain is less.  Sourdough bread has less gluten.  Ozampic siows its entry.
    • Wheatwacked
      You can sell it better if the whole family does gluten free.  If he does have Celiac Diease, it is genetic so either you, your spouse, or both have a 40% chance of also having Celiac.  There are over 200 non classic symptoms also caused by celiac disease not often considered by doctors. Joint pain, muscle pain, muscle cramps, osteoporosis, and allergies for starters.  
    • Wheatwacked
      Hello @MHavoc, thank you for your question and welcome to the clinic. First, has the contstipation abated with the GFD? If your are pursuing further diagnostics you must continue to eat gluten. Each lab has their own reference range for their test, but they indicate an H for high.  Typically anything above 11 is considered positive. Mild chronic inflammation (gastritis) can interfere with intrinsic factor for B12 leading to low B12 causing low MCHC (anemia). So what is causing your gastritis?  A high tTG IgA level generally indicates potential gastrointestinal problems most commonly associated with celiac disease.  Although the biopsy is the Gold Standard for diagnosis, not finding damage in the biopsy does not rule out Celiac Disease. It means they did not find damage where they looked.  The small intestine is over 20 feet long. Many here have been blood positive and biopsy negative, it just delays the diagnosis until you have enough damage to find and fit their diagnostic profile. The Ttg-iga is not only sensitive (90%) but highly specific (98%) and won’t show positive until the damage is severe.  It is estimated that 40% of first degree relatives of diagnosed Celiacs have undiagnosed Celiac Disease, so your sister is a big risk factor in whether you have it. Are You Confused About Your Celiac Disease Lab Results?  This article explains it better and is quite readable. Celiac Disease can cause deficient vitamin D.  Low vitamin D compromises the immune system.  Any other symptoms? liver enzymes?  Recent cold or flue? Celiac Disease and the malabsorption it causes through vitamin and mineral deficiencies can elicit symptoms not usually associated with Celiac Disease. Case in point maybe your gastritis and anemia.  
    • MHavoc
      As with most of the people that come here, I have questions and need perspective/info from this wonderful community.  Some background, started having severe constipation that would not abate even with softners (not really fun to talk about), so I was able to finally get in to see my primary and she scheduled some blood work.  One of things she wanted to test for is Celiac Disease due to my sister having celiac disease since a young child. Here are my test results: MCHC = 31.4 so considered slightly low TISSUE TRANSGLUTAMINASE AB, IGA = 78.8 H So with that result, I was scheduled for an endoscope for confirmation of celiac disease, but I am very confused with the results: Diagnosis 1. Duodenum, biopsy: -No pathologic alteration. 2. Stomach, biopsy: -Mild chronic inflammation with reactive epithelial change -H. pylori not identified on immunostained section. -No intestinal metaplasia or dysplasia I am now scheduled to meet with a GI Specialist from the Celiac team, but that won't be until after the New Year.  I would appreciate thoughts about the biopsy report to understand whether it confirms the celiac disease as was indicated by the blood test results. I have been gluten free for two weeks and it is a very difficult adjustment for me as an older 50+ person.
    • Vozzyv
      Anyone else have intermittent left ear ringing and outer right ear pain? Both seem to happen in the evenings. 
×
×
  • Create New...