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I have had multiMulti symptom cough and cold Multi vita bets and fluoride and iron Multi-betic Multi-day Multi-day plus minerals Multi-day with calcium and extra iron Multi-day with iron Multi-delyn Multi-delyn with iron Multi-symptom nighttime nodular thyroid for three years. "The right lobe measures 5.6 cm.x 2.0 cm x 1.9 cm. Left lobe 5.2 cm x 2.0 clm x2.0 cm x1.9 cm. Echogenicity of right lobe is diffusely inhomogeneous. It has a nodular texture because it is actually composed of numerous thyroid nodules the margins of which are difficult to differentiate from one another. Measurements difficult to acquire. Adjacent to the r. margin of the isthmus there is a solid 2.9 cm thyroid nodule. No dfinable margins. Adjacent to this nodule are at least 2 hypoechoic areas each measuring 5 mm in size and may represent cyusts. The isthmus is thickened. It contains no definable masses.
The echogenicity of the left lobe is inhomogeneous similar to that seen on the right. The l. lobe contains several thyroid nodules some of which are isoechoic with adjacent tissue whereas others are hypoechoic." 8/22/06 No treatment, no medication given. Just watch.
I recently went to another Doctor whose slide showed "follicular neoplasm". He advises a Total Thyroidectomy, for which I am scheduled sometime in Dec. or January.
Thanks for that good information. It seems best to have the TT. Your input helps a lot with my decision. . I'll be going to Mass. General in Boston and have a lot of confidence in the Doctor there. Univ. of PA has a great reputation too. I wish the surgery could be sooner . Did you have a sore throat before your surgery?
Hey there,
I had a TT a little over a month ago. I had a nodule the size of 2cm on one side and 2.5 cm on the other side. They did a needle biopsy and suspected papillary carcinoma. Turned out that they were not cancerous, but I am happy to have the gland out. Prior to the surgery I had a sore throat, scratchy voice, trouble swallowing, and trouble breathing. From what the surgeon said, my gland had enlarged in such a way that it was restricting the muscles in my throat and blocking my airway.
Good luck with your surgery. You will find that your wound from the surgery will heal fast, but the muscles and nerves underneath will take awhile. Also, it will take awhile for your body to get used to missing part or all of the gland. You might experience emotional swings, fatigue, etc... just be patient with yourself and remember that it may take a few months before you feel more like ayourself.
Nanticokecreek was the first place I went swimming in Endicott, NY. I can still see the clear water and the pebbles on the bottom. I guess I am in for a sore throat then. I've had one for a year, but, not too bad. It's getting worse. You were lucky that someone discovered it on that physical exam. Hope you are feeling all better now.
Thanks for your input. You people are wonderful. That's just what I have...a sore throat, voice which seems to slip out of gear sometimes, and, wheezy ......swallowing is scary sometimes. I'm afraid of aspirating. Will be glad when the surgery is over, though I don't like to have to depend on a pill to live.
Do not worry about the pill. I have been on thryoid replacement med for 10 years now. The way I have managed taking the pill is:
I set my alarm for 5:00 am. I have my water and my meds beside the bed each night. When the alarm goes off, I wake-up, take the pill and go back to sleep for few more hours.
This solves 2 issues... 1.) I am reminded to take the pill at the same time everyday 2.) I am taking the pill on an empty stomach for maximum absorption and I give my body enough time to absorb the med. The pill requires a wait of 1 hour before eating food. And another tip, wait 4 hours before eating anything with fiber, soy or calcium. They all affect the absorption of the meds.
The hardest part with the meds is getting the dose right. Just be patient with your body. It usually takes 6 weeks or so for your body to adjust to any change in your meds. And try to get your doc to ease you into the meds. (Slowly increasing your dose). This will help keep your body from freaking out.
I understand you wanting to have the surgery as soon as possible but be patient... If your crew is the best - they know what they are doing. I suggest the following before surgery:
1. Ask your Dr. if there's anyone you can talk to that has had the kind of surgery you are about to have?
2. Be prepared. Ask him EXACTLY what to expect after the surgery. Will you have drains? If so, how long? Should you expect swelling?
3. How many days are you supposed to be in the hospital?
4. Have you had an MRI? Ask Dr. about having one before surgery if you have not...
I went in the surgery room completly unexpecting what they were going to do. Knowing wouldn't of made it any easier but it would of helped me prepare emotionally. If all they are doing is taking out your thyroid - great, but you need to know what's going to happen without any suprises.
Good luck to you. Don't loose the faith - it's the only thing that really helped me get through.
Your thyroid description sounds like what mine was. My symptoms were the voice going scratchy from time to time, pain when I could feel one of the cysts getting inflamed (like a zit inside my neck), the feeling I was going to choke when swallowing food, and the feeling that I always had a really tight turtleneck sweater constricting around my neck. My doc found follicular neoplasms and she was worried it was cancer so she recommended TT. I had the surgery 2 months later (that's how long it took to get an operation appointment at my hospital-- a regionally well-respected teaching hospital). Biopsy showed it wasn't cancer, but it was thoroughly disgusting (my opinion based on the report). Took a week off work, recovery was easy, and all has been well. The scar faded swiftly and now is imperceptible unless you know to look for it. I have none of those awful symptoms I had before, plus there's no unsightly goiter or neck swelling anymore. I used to look like I had a fat neck.
Thank you all for your input. I got lost on this website or would have written sooner. I am going in for a probably TT on Jan. 23. Yes, I am waiting a long time for the best Doctor, so I don't mind. Taking the pill doesn't sound so bad. Looking forward to no sore throat, no swallowing issues, and, of course the fat lump in my 'bow tie' section being gone. The Surgeon said I had a 1 in 3 chance of it being malignant because of the thymic irradiation as a child. It's nice that he tells the truth. I would rather know, even if it's bad. After all this, it probably will be benign. I'm sure it will be thoroughly disgusting whatever it is because it just feels that way. Thanks a million again!
hi michelle here i just had my right side out 3 weeks ago when i was at hospital they were looking for neoplasm cancer like u i get my pathology results back today mine grew extremly fast and was pressing against my wind pipe it still feels like somethings stuck in my throat i dont know what but my left side was healthy.
Dear nanticokecreek,
"Follicular neoplasm" in FNA includes benign and malignant follicular neoplasms. The only way to differentiate the benign and malignant is to prove of tumor capsular invasion in histologic section (exam by pathologists), that's mean TT. Good lunck for the operation :)
Dear Nanticokecreek
It's been over 30 years since I had a total thyroidectomy due to cancer. Although it is important to be consistent, thyroid replacement medication has a half life that is long enough that you don't notice if you forget to take the pill one day so don't be very concerned about that aspect.
Check out the thyroid cancer survivors website, it has lots of helpful information. http://www.thyca.org/thyroglobulin.htm
I just had a TT last Monday. The operation went great. The reason was I have had a complex cyst on my left lobe for five years which I have ultrasounded every six months. In a recent biopsy the results came back with "possible follicular neoplasm". Because I had three small nodules, cysts, on the other side, the doctor opted for a TT. I go back Tuesday for results. I am scared that it will come back with cancer. Any advise, or similar situations?
I recently had a FNA and the diagnosis was follicular neoplasm. Instead of a TT I would like a diagnostic lobectomy, which is where they only take half of the thyroid, the one with the nodule, with the main purpose of doing pathology on it. If it turns out not to be follicular cancer, then the other half could likely provide enough hormones so I don't need the pill. In my opinion, jumping to a TT is too aggressive for me anyway, but it also depends on your particular circumstances.
I am a 28 year old male, and I found a lump on my thyroid (right lobe,2.7x2.0.1.5 cm). FNA result came back as "Follicular Neoplasm, probably benign". My doctor recommended a hemithyroidectomy, I am on a waiting list for an operation, but my doctor seems to think it's routine and has not flagged as urgent, which means a fairly long wait (a few months). This is the UK National Health Services, so I am not paying, but the flipside is that there are long waiting lists.
My question is, how risky is this wait? Is my doctor right to consider it a routine procedure? I just need some peace of mind, since no one seems to have an answer to this question.
Since April 2005 I was diagnose with a slight inhomogenous and hypoechoic nodule in the upper right pole. I had a FNA done, the results were insuffient cells to determine. In Feburary of 2009 I had another ultrasound done. I was told I had another nodule in my left lobe. I had another FNA done the results on the rt lobe stated unsatisfactory for evaluation, only rare follicular cells are seen. the left lobe favors a goiterous process or an adenomatoid nodule: howerver follicular neoplasm cannot be entirely excluded. I sat with a Military doctor yesterday who advised me to keep watching it and follow up in 3 months. Iam scared and need some advise.
I was also diagnosed w/ follicular neoplasm by FNA. 4 yrs ago I had an US of the thyroid which should multiple nodules on both sides. I had another US in Nov 08. The nodule grew half the size from 4 yrs ago. I am scheduled for a minimally invasive TT Friday. My sister just had a TT 6 weeks ago and she was found to have papillary CA and today she will be in isolation due to the radioactive pill. Her thyroid grew into the chest area and wrapped around her trachea and esphosagus (sp?). The MD said it was just a matter of time before it would attack her aorta.
Please check out your MD to make sure he has done plenty of this type of surgery. My MD specializes in endocrine surgery.
Reading all your comments have eased my mind. I am having surgery on Thursday, July 30th. I appreciate the possitive thing said about recovery. I teach middle school, therefore, I will have to tone down my voice.
Being a teacher as well, I was totally apprehensive about surgery. Had to have a TT for a large goiter and follicular lesion on the left. Voice came back immediately but please rest your voice as I was told. I did not have any calcium drops as of yet so 2 out of 3 isn't bad for my worries. The third was cancer which it turned out to be. So when the other posts talk about follicular neoplasm and possibility of cancer, it turned out to be so with me. Glad to have the TT taken care of on July 20, 2009, and now it is RAI for me in September to rule out any cancer cells. Do you go back on August 10th like a lot of us in Southern California for public school? Hopefully you have more time off to recover from the TT. I haven't been able to turn my neck yet and it is one week out (essential for driving). Take care.
Was glad to have gotten it out.
Funny about your user name, thought you might be from PA as there is a town called Nanticoke near us here!
Good luck.
I had a TT a little over a month ago. I had a nodule the size of 2cm on one side and 2.5 cm on the other side. They did a needle biopsy and suspected papillary carcinoma. Turned out that they were not cancerous, but I am happy to have the gland out. Prior to the surgery I had a sore throat, scratchy voice, trouble swallowing, and trouble breathing. From what the surgeon said, my gland had enlarged in such a way that it was restricting the muscles in my throat and blocking my airway.
Good luck with your surgery. You will find that your wound from the surgery will heal fast, but the muscles and nerves underneath will take awhile. Also, it will take awhile for your body to get used to missing part or all of the gland. You might experience emotional swings, fatigue, etc... just be patient with yourself and remember that it may take a few months before you feel more like ayourself.
Good luck to you. I wish you a speedy recovery.
I set my alarm for 5:00 am. I have my water and my meds beside the bed each night. When the alarm goes off, I wake-up, take the pill and go back to sleep for few more hours.
This solves 2 issues... 1.) I am reminded to take the pill at the same time everyday 2.) I am taking the pill on an empty stomach for maximum absorption and I give my body enough time to absorb the med. The pill requires a wait of 1 hour before eating food. And another tip, wait 4 hours before eating anything with fiber, soy or calcium. They all affect the absorption of the meds.
The hardest part with the meds is getting the dose right. Just be patient with your body. It usually takes 6 weeks or so for your body to adjust to any change in your meds. And try to get your doc to ease you into the meds. (Slowly increasing your dose). This will help keep your body from freaking out.
Best wishes to you.
Just read your story...
I understand you wanting to have the surgery as soon as possible but be patient... If your crew is the best - they know what they are doing. I suggest the following before surgery:
1. Ask your Dr. if there's anyone you can talk to that has had the kind of surgery you are about to have?
2. Be prepared. Ask him EXACTLY what to expect after the surgery. Will you have drains? If so, how long? Should you expect swelling?
3. How many days are you supposed to be in the hospital?
4. Have you had an MRI? Ask Dr. about having one before surgery if you have not...
I went in the surgery room completly unexpecting what they were going to do. Knowing wouldn't of made it any easier but it would of helped me prepare emotionally. If all they are doing is taking out your thyroid - great, but you need to know what's going to happen without any suprises.
Good luck to you. Don't loose the faith - it's the only thing that really helped me get through.
Take care,
LB
Best wishes!
"Follicular neoplasm" in FNA includes benign and malignant follicular neoplasms. The only way to differentiate the benign and malignant is to prove of tumor capsular invasion in histologic section (exam by pathologists), that's mean TT. Good lunck for the operation :)
It's been over 30 years since I had a total thyroidectomy due to cancer. Although it is important to be consistent, thyroid replacement medication has a half life that is long enough that you don't notice if you forget to take the pill one day so don't be very concerned about that aspect.
Check out the thyroid cancer survivors website, it has lots of helpful information. http://www.thyca.org/thyroglobulin.htm
I recently had a FNA and the diagnosis was follicular neoplasm. Instead of a TT I would like a diagnostic lobectomy, which is where they only take half of the thyroid, the one with the nodule, with the main purpose of doing pathology on it. If it turns out not to be follicular cancer, then the other half could likely provide enough hormones so I don't need the pill. In my opinion, jumping to a TT is too aggressive for me anyway, but it also depends on your particular circumstances.
I am a 28 year old male, and I found a lump on my thyroid (right lobe,2.7x2.0.1.5 cm). FNA result came back as "Follicular Neoplasm, probably benign". My doctor recommended a hemithyroidectomy, I am on a waiting list for an operation, but my doctor seems to think it's routine and has not flagged as urgent, which means a fairly long wait (a few months). This is the UK National Health Services, so I am not paying, but the flipside is that there are long waiting lists.
My question is, how risky is this wait? Is my doctor right to consider it a routine procedure? I just need some peace of mind, since no one seems to have an answer to this question.
Please check out your MD to make sure he has done plenty of this type of surgery. My MD specializes in endocrine surgery.