Anyone have thyroid issues as well as BC?
Comments
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I just wanted to add a comment on something rianne said in her OP. "My thyroid levels are perfect."
What I think I now understand is that a thyroid panel measures the amount of thyroid hormones in the blood. However, this may not tell the whole story. Evidently other things (such as bromides in processed bread, for example) compete for and utilize the same receptors in our tissues that these necessary hormones use. So even though it's possible to have perfect thyroid readings, our tissues (including breast tissue) may still be deprived of what's needed for optimum health.
That's a very simplistic explanation, but I thought it was worth sharing. Perhaps someone with more scientific expertise can elaborate. Deanna
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And why in the world am I the exception that confirms the rule? lol
No thyroid hystory in my family. No BC history. I'm hyperthyroid. The only thing that could have been a factor was my Vit D levels depleted by the hyperactivity of the thyroid. But still that was in the last four years only and the BS said that tumor I had was there for at least 10 years, he thought more like 20 - long before my thyroid started acting up.
Sigh. There's a lot of guesses and I doubt it will be found out soon.
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Hi,
I never got a biopsy report. My BS had referred me to an endocrinoligist and my Oncologist told me to cancel it since he would treat me. I will ask for a copy of it tomorrow when I see him. On the day I had the biopsy, the man who performed the procedure told me I had just a "run of the mill" boring nodule and that he was 100% sure it was not cancer. He was really nice but that procedure was awful and to make matters worse, I had my first AC chemo treatment the day before and I wasn't allowed to eat or drink anything until noon the next day. I was one sick woman.
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I've had 4 nodules on my thyroid for about 8 years now. One is larger than the others, and has been biopsied twice, always benign. I was diagnosed with bc 2 years ago. After 6 mos. of chemo, rads and now femara....surprisingly, they have all shrunk, as has my goiter. My endocrinologist does US every year on them.....nothing concerning, no vascular component to them. My thyroid levels are all normal.
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Here are some stats on the correlation between hypothyroidism and bc. Hyperthyrodism doesn't appear to carry the same increased risk. http://www.ncbi.nlm.nih.gov/pubmed/9061284
Day, did you ever have an injury to your breast? Or an autoimmune condition? I've read that both of those can contribute to developing bc at some point. (Or maybe hyperthyroid is an autoimmune condition, in which case it would tend to mess up your immune system and possibly distract it from where its needed -- like knocking out those bc cells.) Deanna
Editing to add another interesting link. This one may even contradict the previous one... not sure... I haven't been able to fully concentrate on either one of them, but wanted to pass them along: http://www.ncbi.nlm.nih.gov/pubmed/15917958
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I was hyperthyroid and then had the thyroid removed, which caused me to be hypothyroid (meds everyday for the rest of my life). I will definitely get my blood tested to make sure the meds are still at an effective level.
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dlb - yes, I have Graves Disease that causes hyperthyroid, but it's kind of hard to believe that there is a connection (at least in my opinion), as the antibodies that in Graves Disease attack the thyroid and the eyes' soft tissues are specific to it, and have nothing to do with cancerous cells. And I never had an injury to my breast (s). The left one, that I had the prophylactic mastectomy on, was in the last stage of ADH right before it turns into DCIS, on a 6 cm area. I always had ultra dense breast tissue, with no fibrocystic disease.
Both my endo and my BS said I am an exceptionally rare case, as usually patients with Graves, especially the ones that have a high degree of thyrotoxicosis, do not develop breast cancer unless they get in hypothyroid state after thyroid ablation. That, combined with the muti-typal, muti-focal tumor I had (that is about 1 in 100,000 cases) makes me be a very special case. I wish I wasn't. sigh.
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Like so many here ... I've had thyroid issues .. dating back 20 years .. HOWEVER, I ended up with thyroid cancer .. a total thyroidectomy, along with radium treatments in the hospital to kill any and all thyroid issue .. and have been on synthroid for years, varied doses depending on my blood work...
Fast forward 20 years, now Breast Cancer ! Association between the two cancers - I say yes.
Strength and Courage to all.
Vicki Sam
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Rianne, please see an endocrinologist. I was dx'd with thyroid cancer 4 years ago and with bc May 2010.
If you talk to your Dr.s they will tell you there isn't a link between the two. I disagree. A few months ago I went to a BC support group meeting and 50% of the women had problems with their thyroids before BC.
If anything, just make sure it isn't anything serious.
Hugs,
Jules
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Jules,
Scary statics! Thank you for sharing.
Vicki Sam
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I have hyperthyroidism, at 16 I was dx'd with Hodgkin's an on a yearly check up my Ongologist noticed a lump in my neck. I have gone for several biopsy and all have come back beign. Prior to being dx'd with BC there was discussion about removing the thyroid due to my past medical history but when I seen my doctor he did nothing just said to make another appointment. I have been on 112MG of Synthroid for about a year and a half now and it has helped with the goiter but there is still a small on there, possible why my doctor wants to remove it. I have also been on 20MG of Tamoxafen since January.
I have my next appointment regarding my Thyroid in early April, just wondering if there is any questions I should be asking as I have not looked into any connection between Thyroid problems and BC.
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JanetinVirginia - you described my thyroid history exactly : papillary cancer in the left node (removed, no radioactive iodine) in 1995, followed by a benign nodule in 1996. I've had a total thyroidectomy, and have been on synthroid since the second surgery. A recent ultrasound of my thyroid showed a small mass that requires follow-up, so I will have the ultrasound needle-guided biopsy next week. Just when I was celebrating no new/major procedures for the year! I'm not overly worried, but just wondering how long this has been present (it's not palpable), and what caused it.
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Blue, there a gazillion other cells in the body with iodine receptors, not just those in the thyroid.
I had a thyroid lobectomy many years ago and take Synthroid. I suppose that's a positive as I don't have to worry about Femara and hyperthyroidism as much. But then again maybe that's what's causing my new (benign) nodule.
edited to add: I just read the last page, Day's comments in particular. Re-do: Maybe I want to be hyperthyroid again!!! Hopefully all the exercising I do now raises my thyroid hormone levels enough.
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I'm glad I found this thread, I didn't realize how many others are dealing with both thyroid & BC issues! My grandmother died of thyroid cancer, her daughter, my mother, died of BC, and I was diagnosed with BC in 2008, then hypothyroidism in 2009. When I went for genetic counseling, the counselor wanted to know what type of thyroid cancer my grandmother had. Unfortunately I have no way of finding out, but she said there is a faulty gene that can cause one type of thyroid cancer AND breast cancer.
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I am another one who was dx'd with ThyCa less then 2 yrs after my BC dx...had partial thyroidectomy (right) last November, take 30mg of Armour daily and declined RAI. I will have my first labs next week to see how my TSH levels are.
I had alot of SE's and pain issues after BMX and Chemo. Took Tamoxifen for 8 months but was so miserable I stopped 2 months before my ThyCa dx. I will admit that I am feeling so much better now then I have since my original BC dx. Other than LE issues and weight gain, I am almost back to 'normal' or a least a new normal that I can be happy with.
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I'm coming late into this thread. I have been on arimidex for almost 4 years. My thyroid levels were normal until early this year. 2 Tests since January and the numbers are going lower. I have an appointment with an endocrinologist May 13 (a heck of a time just getting an appointment) I mentioned this to my onco earlier this month and he just said they (oncology) does not do blood work on the thyroid, my regular Dr did that. I had 30 treatments of radiation 4 years ago for Stage 1 BC.
I do not have any symptoms or at least any symptoms I'm reading about. Should I bring this up to my oncologist again or just wait til I see the endo next month. After reading all these posts, now I'm concerned.
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I've been hypo thyroid for over 15 years, and have a few thryoid nodules that have been monitored by ultra sound for several years one is known to be hot.
I had a thyroid scan between my chemo and radiation treatment -- all the nodules had shrunk.
The next year the scan showed that some had shrunk and some had gotten larger. I was sent to the endocronolgist. The PET/CT scan taken before the BC surgery had shown thyroid activity.
I was scheduled for a needle biopsy and let my bc team know. The biopsy was benign, but showed lymphocytes. I had a TPO test that confirmed that I have Hashimoto's disease -an auto immune disease.
When I talked to my oncologist, she said it was a timing issue. The chemo had blown away my imune system, which in turn was not inflaming the the thyroid -- so the nodules shrank. When my immune system came back it renewed its attack on the thyroid, inflamming the nodules and causing them to enlarge.
Side note: Inflammation shows up positive on PET scans. Also 1 in 5 women will be diagnosed with Hashimoto's in their lifetime.
The other thing that has happened is that my TSH has gone wy down (below .2) while the T4 has remained normal. The endocrinologist is iterating my synthroid dosage downward. I've been on Femara for a little under a year and a half.
Thyroid problems and breast cancer are both more prevelant in women than men, I wonder if that's the reason that ther a bunch of us with both issues.
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I am so glad I found this thread. I am going to a specialist to ask for a fine needle biopsy of a adenoma the GP found on my thyroid. The GP wanted to do the cold, warm, hot test with the radioactive dye which the endocrinologist (from a previous visit) was reluctant to do. I am also 2 1/2 years out from dx. Of course I don't want to worry, but ya know????
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Hi Girls - I have a large goitre and have refused surgery so far as I couldn't cope with it just after the whole bc times 2 thing. My mother has had 2 goitres removed. My thyroid function is normal. I always try to use iodised salt and over here our bread has idiosed salt in it, so that helps some.
The studies say there is no link between thyroid issues and bc, however, in Japan where they eat a lot of seafood, there is a low incidence of bc. The breasts process iodine as well as the thyroid. There are so many of us with thyroid issues, I can't believe that there is no connection.
Sue
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I finally saw an endo Dr today. My hyperthyroidism is very mild (I have no symptoms) but is inflamed. He did an ultrasound and I am having a thyroid scan early June. He said breast cancer and thyroid issues appear to go hand in hand. He has been involved in a study for about 10 years regarding this. He also said it has nothing to do with my meds (I havebeen on arimidex since August 2007) or the radiation I had, at least in my case it appears. More than likely one of my parents was hyperthyroid even though it may have gone undetected. So I had blood work done, then the scan, an appointment with him in June.
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So true, Suepen. I am going to ask all three doctors- the GP, the Endocrin..and the onc about this.
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me too! Day I am indebted to you for all your very good info....I am using my primary who is an endocrinologist, and after I'd been on arimidex for about a year (hashimotos) my dose was too high. It took several months to get it right, it went high,then low, etc. GP said this is typical of extrogen inhibiting drugs. I also had an ooph, and she said that does it too, as well as menopause, so anyone around that timeframe, get those levels checked!
Day, what is your "ritual?"
(you look extremely pretty in your photo, btw)
xoxo
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I did do lots of searches trying to find out if there was a connection. In one group of bc patients over half of them had thyroid issues, but the study did not conclude there was a connection - totally crazy. They say that thyroid issues are very common these days due to our diet. I might do some more searches and let you know what I find.
Sue -
Hello everyone
I've posted on other threads about my thyroid issues and my frustration with my endo limiting testing to TSH and T4 even with a BC dx !!! I am so frustrated with him. All he'll admit to is that I need "monitoring" every 6 months because of the Tamox.
Here is what I found on my searches, the tests I'm going to try to get my "caretakers" to do to thoroughly test my thyroid function, wish me luck:
- 1. TSH
- 2. Free T4 and Free T3 (note the word "free"-important since it measures what is unbound and available.)
- 3. Reverse T3-to be done at the same time you do the Free T3. Then calculate your ratio with the results and measurements.
- 4. Thyroid Antibodies (anti-TPO and TgAb. need both.)
- 5. Ferritin, % Saturation, TIBC and serum iron (all iron related labs)
- 6. Adrenal Cortisol levels (but we strongly recommend saliva tests, not the one time blood test your doctor will do).
- 7. B-12 and Folate
- 8. RBC Magnesium and Potassium (rather than serum), plus Calcium, Sodium, Glucose (part of Metabolic panel, though you'll need RBC for above)
- 9. Vitamin D (25-hydroxyvitamin D
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I was diagnoised with hypoglycimia at age 5. Started having symptoms of Hypothyroid and adreneal issues 10 years ago. Took two years, 2 hospitalizations, and visits to 2 endo (both said I was depressed and needed anti-depressents despite the lab work screaming HYPO HYPO HYPO) Final found a naturalpath who read the labs and prescribed Armour thyroid.
Then, life was good.... However, I found the BC this January and I wonder if the the tumor started 10 years ago when the hypo flared up. Same time frame...
But, there are issues. I am doing chemo, then surgury, then radiation. Before I started chemo, my regular doctor (not the natural path) did a full physical with a bunch of labs including my TSH. That score came back unreadable (less than .001). Regular doc wanted natural path to look at it and adjust the Armour - a most regular docs do not deal with it. Natural path can't see me - every call is another excuse - and it seems like the breast cancer is a bit of a difficulty for her.
So, the Family doc (with the oncologists recommendation) sends me to another endo. This one is right out of med school and Armour is evil beyond reason. She wants me to switch to synthroid. I then show her my chemo schedule and ask how would we be able to tell if a new side effect that pops up is from the switch in thryoid or from the chemo? If you look at the lists - the side effects for Hypo and Hyper thyroid are identical to side effects from Taxoterin (spelling) and Cytocin. She demands that I make the switch immediately.
Back to oncologist. He is referring me to another endo. Oncologist is not keen on the switch midstream, but he agrees - I am taking too much. I hope that I can get in next week. In the mean time, I dialed down the armour - and Endo one had given me lab papers so I got my TSH, Free T3, and Free T4 tested this week with a repeat in 4 weeks. I dialed down the Armour by a pill and if I have to, I will use her second lab papers to get the results in four weeks to see what happens. I would like an opinion from a non-hysterical, non-judgemental endo though - and personally I do not think they exist.
However.....
I think being slightly hyper has shielded me from some of the more aggressive side effects - for example, my bowels are working fine. And, there is research out there that the chemo drugs and the steroids that we take effect the thyroid, the adrenal glands, and blood sugar. I am sure that the AI and Taxofin will also screw it up to.
So, if anyone knows of an endo who is familiar with both breast cancer, sugar glucose levels, chemo, estrogen levels, and thyroid in the Chicago - Milwaukee corridor - please PM me their name......
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Hello Pebee,
"I would like an opinion from a non-hysterical, non-judgemental endo though - and personally I do not think they exist."
I so agree with you, either they own shares in anti-depressants pharmacos or are limited to treating diabetes.
Mine wants me to do a sleep study, WTH...!!!! I figure I've been tested inside out for the past 18 months, sooo sick of being tested, and going through a sleep study is NOT going to help me.
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One of the reasons I don't want my thyroid removed is the suggestion that thyroid hormones cause breast cancer. Here's one article on the subject. It also mentions the low incidence of bc in Japan.
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That article is from 2006.
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Hi everyone, This is my first post on this discussion group and I am telling my story because it may help some of you. First I think there is a relationship between thyroid and breast cancer. They just haven't done enough research to know the impact of thyroid on breast cancer and vice versa. I think the oncologists and endocrinologists should read these discussion posts. For years I have been taking methimazole to control thyroid hormone levels since I had a "hyperactive thyroid" due to a benign nodule. In Dec 2010 after a routine mammogram they found what at first they thought was DCIS after a breast biopsy. Got a second opinion on the pathology of the DCIS at Mayo clinic and they did further workup. A chest xray and then later a cat scan, revealed a 7 cm growth going from my thyroid and then down and behind the sternum. Due to the location they could not biopsy it, I ended up with a mastectomy and axillary node dissection in January 2011 and a thyroidectomy in February 2011 They could not do both procedures at the same time due to length of surgery and risk of complications. The good news is that the thyroid growth was benign and the bad news was that the DCIS was not DCIS but invasive breast cancer with some lymph node involvement. So now I am on chemo for 6 infusions and then herceptin for a year. . Had to wait a little longer for the chemo to begin because the incision had to heal from the thyroidectomy. In 2009 I had a chest xray and this large thyroid growth was not there. So was there a connection between the development of the cancer and the rapid growth on my thyroid which developed in 1 year, I know that there is no definitive answer here.
Recommendation: If you have thyroid issues and breast cancer issues, insist on being carefully monitored.I am going to try and get my endocrinologist and oncologist to speak to each other more. If your situation is going to "tumor board" ( like a patient care conference) tell them you want the endocrinoloigst to participate as well. I have now gained 15 pounds in the past 14weeks since the thyroidectomy and chemo infusions and I wonder if the chemo is impacting the effectiveness of the thyroid supplement. If you have any suggestions on what to ask the endocrinoloigst or how to stop the weight gain please let me know. I weigh and measure my food and do not eat sugar or flour.
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Thanks, Serenity Wisdom-Very helpful.
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