I had a biopsy (FNA) last month and one of the nodules was identified as thy3f. My endocrinologist rang me and said usually what happens is a hemi-thyroidectomy and one of her colleagues would be in touch. So I prepared myself mentally for surgery and then her colleague (another endocrinologist) informed me that she doesn't think I need surgery but a surgeon will make the final decision.
I have no idea who this surgeon is or when they will be in contact but it sounds like they are just going to assume it isn't cancer which is odd as I've had cancer (leukaemia) multiple times before which involved my neck being irradiated (so increased risk of thyroid cancer).
I'm just a bit confused, has anyone experienced something similar please?
Hi KaspianSce
Sorry that nobody got back to you sooner, cannot say I have any experience of thyroid cancer as my wife's cancer is very different.
I have however been through examples of doctors trying to find answers when things are not quite so clear cut as we might hope and also different specialists passing us from one to another - it is really quite worrying.
Fingers crossed you get to talk to the surgeon before too much longer but then you finally get an answer.
<<hugs>>
Steve
Hi src60,
Thanks for your reply, it definitely sounds like you can relate to that feeling of being passed around. I think I've gone from endocrinology to another endocrinologist and hopefully to an ENT surgeon. The whole thing has become overwhelming and I don't want to pay too much attention to being told I probably don't need surgery in case I do need to.
Thanks, I might ring my late effects team in a few weeks if I haven't heard from the surgeon.
Hey,
I had two FNA's one was THY3A and the second came back THY3F, the second was done while waiting for an appointment with the surgeon and as I had been diagnosed with Graves disease before hand we opted for full Thyroidectomy otherwise he would have done half as there was suspicious features... After the removal it came back as Follicular Variant of Papillary thyroid cancer.
Before being referred to surgeon there was 3 MDT meetings about me.
Hi TrinityTrace,
Thanks for your reply, I've just had the one FNA and was told it was a follicular neoplasm (thy3f) and they wanted to take out a capsule and blood vessels as they couldn't tell if it was cancer or not. I was comfortable with this approach but now there has been an MDT and I've been told I don't need surgery but I would like them to explain this decision to me.
I've emailed them today so will see if they reply, hope you are doing well post removal.
I am doing ok thanks, a few side affects of my high dose Levothyroxine but about to have risk stratification done so hoping that comes back low risk so they can reduce my medication more!
175/150 mg alternating dose was just 175 and have loads side affects, diarrhea, weight gain, palpitations, fatigue, low mood, insomnia!
Grrrr lol
Hopefully they answer your email quickly and explain their decision!
Let us know x
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2024 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007