New on the forum... letters meaning ?
Good evening,
So, here I am. 34 y.o., french, int the USA since 2012, married, mother of 3... and just diagnosed with a Invasive Ductal Carcinoma - IDC so ? This are the only letters that meant something for me on the forum lol
I know I'm on stage 2, that i'll have a mastectomy soon. When ? No idea yet. I know there is multiple lumps, size around 4cm. And that's it. Everything else will be sorted out after the mastectomy.
I see a lot of profil with a lot of letters, meanng i'm sure a lot of things but I don't know what. I tried to find a post with explanation but it is a huge forum.
If anyone could let me know all the meanings... thank you.
Comments
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Hi Sol and welcome. There is a key to terms under Help and here: https://community.breastcancer.org/forum/131/topic...
I am so sorry about your situation. Are you getting good advice from your surgeon? Do you feel good about choosing a masectomy? We are happy to help you.
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Hi Sol,
It can be overwhelming at the beginning, especially with all the acronyms and technical jargon; but if you have questions (about mastectomy or anything else) and prefer to discuss in french, don't hesitate to PM me - ça me fera plaisir de te répondre
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Well, I didn't even think about doing something else. She told me I needed a mastectomy - it is too big to save the breast and too close to the nipple also, I'll lose that - and we'll see the rest after that...
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Oh and, sorry, thank you for the link Georgia ! I'll have a look !
Merci Sourisou, mon anglais est parfois un peu limite... je n'hesiterai pas !
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Happy to help SoL. This is a useful thread on masectomy you can read: https://community.breastcancer.org/forum/68/topics...
And thank you Sourisou! I do not speak French and am grateful for your expertise.
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Hi Sol and welcome. After ultrasound my tumor was estimated at 3.6 to 4.5. cm. (After surgery 5cm) I did have a unilateral skin sparing mastectomy (tumor directly under the nipple so it had to go) with direct implants and I don’t regret it. But, I had a team of doctors (most hospitals have a tumor board) and a lot of different tests (FSH, mammoprint , MRI) before deciding on my treatment plan. It is ok to ask for 2nd opinions and to fully understand why a treatment plan is being recommended for your particular situation. If you haven’t spoken to a medical oncologist I would strongly suggest asking for a referral for one before any surgery. They are wonderful at explaining pathology. If you had a core biopsy they would be able to tell you about the ER/PR status,tumor grade, LVI and HER2. They can also order tests like a mammoprints that tests the tumors genetic makeup. All pieces of the puzzle that let you pick the best treatment plan for you. Good luck and keep us posted
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Thank you Meshell5324 for your answer !
After mammogram and Ultrasound, my tumor is estimated around 4 cm and they do plan a unilateral skin sparing mastectomy, (under the nipple to so it also has to go) but they can't reconstruct right away as there is a risk I need radiation and they told me they can't reconstruct before we are done with treatment. I guess that's the big difference between our case... I
I did meet a medical oncologist and she stayed with me quite some time but basically, I'll see her 2 weeks after the surgery for the treatment plan...
I had a core biopsy but they didn't give me the results. As I can now see what all the acronyme means, I can say that I am ER+, PR- (at least, they told me I will need something for the estrogen nothing about the progesterone so I assum that's my results). The first lymph node didn't seem to contain any cancer at the biopsy but they'll check that during the surgery by doing a full exam on it - as I've been told. I have no idea if i'm HER2 negative or positive, I guess that changes a lot of think and that is definitely what I'll ask them tomorrow. I also don't know what is the tumor grade, that's what I'll ask also !
I did started the genetic testing, I'll know this answer soon enough ^_^
Thank you all for your answer and questioning, it helps me see a bit more clear in all those info !
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Hi Sol- my breast surgeon was almost positive that I would need radiation after my mastectomy. She wasn’t a big fan of me doing DTI (direct to implants -not because of the radiation but because of circulation/blood flow, I wanted over pectoral) she did however recommend having TE (tissue expanders) I wasn’t interested in DIEP reconstruction. I found a wonderful and experienced PS (plastic surgeon) who did over pectoral reconstruction. She was fully aware that there was a very good chance I would need radiation treatment after surgery. She was really well informed on studies done on reconstruction with radiation- at Sloan Kettering (DTI) MD Anderson (TE). If you have the TE put in you would need to wait until a minimum of 6mths after completion of radiation treatments to do your exchange. She also went over what could go wrong after the radiation and how she could fix it. Thankfully my after surgery pathology was really good. My radiology oncologist said I had a 5% chance for local reoccurrence and radiation treatments would not lower that- so no radiation! I’m not saying your situation is the same as mine. I’m just putting it out there in case you want reconstruction at the same time as surgery (breast surgeon goes first and then plastic surgeon follows so they need to coordinate their schedules) and think it can’t be done because of radiation because it can. Second opinion are always good. Try speaking to another PS if it would make you feel better. -
Hi, I'm newly diagnosed with breast cancer, my mammo show dense breast tissue. I had a biopsy Wedensday before Thanksgiving so now I have to have an MRI on Friday.
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Hi Tara-
We want to welcome you to our community, although we're so very sorry for what has brought you here. Do you have any information from your pathology report that might help us direct you to the forum that best fits your needs? We have several, and many members find it helpful to be able to connect with other members with the same diagnosis. Once you have more information about your breast cancer and possible treatments, we can help you find the forums for you!
The Mods
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Hi Tara and welcome. Sorry you are going through this. Personally, I didn't even know I had dense breasts until suddenly a mammogram led to an ultrasound and then to an MRI! An MRI is pretty painless, but there is a blood test first and then the dang machine is super loud. Let us know if you have any questions.
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