Just diagnosed and confused ??
Comments
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ShirleyFaye: I just remembered something about LCIS which I want to share with you. Women can have LCIS for years and years and it's never discovered. It's often only discovered when an invasive lump is found. So that shows you it's not really as threatening as DCIS.
Leaf: We can't help being intelligent. My surgeon didn't like it when I asked too many questions - the prick. I have since dumped him and am now seeing a female one for follow up. I made sure she got the message that I was very informed and didn't like being treated like an idiot. I used to work in medical software so a lot of terms are very familiar to me (I'm a software engineer).
Sue
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Hi sue thanks for all of your help info. All they found on my mamogram that started the whole thing is small area of clustered microcalicifictaions. Then it was magna views and right after that the radiologist came in the room real fast and said we need to biposy the area.so i had no lump that I know of. When I saw the magna views the area had a bunch of tiny dots and I think one small comma shaped area. On the magna view it look like an area the size of quarter. So I had no lump. But then again I have dense areas. I am picking up my mamos on wen and the magna view films. I thank everyone for all of there support. and then will be on to the second opinon next mon. The lady who made the appt said dr funk might want to do her own biposy and I guess thats fine at least I know she will send it to a lab that will interpet the result accuratly.
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Suepen: No doubt you are very smart. I do have to be careful about the 'bigger picture' though. We're probably read more academic papers than most of our general docs, though.
Most LCIS (and nothing worse) does not present with a lump. LCIS (and nothing worse) is usually an INCIDENTAL finding at a biopsy. It often (but not always) is present not *at* but *adjacent to* the 'region of concern' (action at a distance.) I think that if an LCIS woman goes on to get invasive breast cancer, it often happens in an area that was previously thought to be normal. Its hard to tell though, since if it was biopsied and removed, then it would be gone, of course. In a 'small' number of cases, classic LCIS may be a *non*obligate precursor to breast cancer. No one wants to define 'small'.
LCIS (and nothing worse) patients, IF they go on to get invasive breast cancer, get more IDC than ILC (as is the case with the usual population), but many more of the LCIS (and nothing worse) patients get ILC than in the general population.
ILC often presents as a thickenening. It is thought that this is due to the lack of E-cadherin. (Think E-cadherin.) The E-cadherin is thought to be part of the 'glue' that holds a tumor together, making a lump. ILC more often presents as a 'web' or 'layers', and often (not always of course) not as a discrete lump.
Since LCIS and nothing worse is normally found as an incidental finding at a breast biopsy, and of course not every women gets a breast biopsy, we don't know how many women are out there who have LCIS. The number of LCIS cases has increased over the years http://www.ncbi.nlm.nih.gov/pubmed/12353815 , partly because there are more mammograms, and more biopsies than in the past.http://www.ncbi.nlm.nih.gov/pubmed/16604564
In the Li paper, they find that the LCIS and nothing worse patients actually had a higher rate (adding the risk of both breasts together) of subsequent invasive breast cancer than DCIS patients during this period (1988-2001). I think more DCIS patients were caught at a more advanced stage, though.
Among DCIS patients, incidence rates of ipsilateral and contralateral invasive breast cancer were 5.4/1000 person-years and 4.5/1000 person-years, respectively; and among LCIS patients, incidence rates were 7.3/1000 person-years and 5.2/1000 person-years, respectively. http://www.ncbi.nlm.nih.gov/pubmed/16604564
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Leaf: That's what I meant, LCIS can be there and never discovered until a pathology test is done for another reason, not that a lump was always associated with it. In my case I had no idea I had LCIS - it was only found because of the lumpectomy I had.
Sue
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Hello Ladies,
Well guess what I went for the second opinon today and so thankfull I did. The columnar cell lesion is a begnin condition basiclly nothing. just changes in the breast. So no surgury and no radiation. I will have an Mri next month and a mamo on the right breast in nov and regular mamo in may and an mri every year and see the doc every 6 mo. Thank God for all of you knowledgeable woman you all saved me from going through a surgury and radiation I did not need. The doc said the Mri will give me the clean bill of health. :-) and of course they will double check the slides.
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YEA! ShirleyFaye. Sounds like you found a winner in a doc who will double-check and follow you for awhile. That's good news.
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ShirleyFaye: That's great news!!! Makes your original doctor sound really stupid.
I double checked with my new bs yesterday about the LCIS I have left in my breast and she is adamant it's ok to leave it there.
Sue
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Thank you sue was great news and thank to you and all the ladies who told me to get that second opinon. And great news for you to. My doc mentioned diet. So I drink lots of green tea, and take vitamin d 3 liquid and omega 3, lots of greens and not to much meet and def no soy or chocolate.
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Good for you, ShirleyFaye! I echo patoo's post.
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Thank you Leaf
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There you went and did it ShirleyFaye - mentioned that illegal word "diet"!
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Hey patoo, Yes i know sorry lol thats what the doc said, so i have been drinking green tea, taking vitamin d3, omega fish oils and tumeric. yeah not so fun but getting used to it now if i can only get on my bike and go for a ride would be doing good. lol
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Oh, you can get on that bike. Come on over to the exercise thread and join us - it will get you going.
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sure where is the thread
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bumped it to top a few minutes ago.
http://community.breastcancer.org/forum/58/topic/741082?page=69#idx_2048
We have fun.
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Hello ladies hope you are doing well. here is the latest on my stats it is a roller coaster ride. After all being said. My dr order a Mri with and with and with out contrast. And an area lit up it is 1.6cm x 1.2 cm x 1.7cm and they have me listed as a BI rad -6 now. So next fri I am off to sugury for a needle loc with a mac anathesia. Boy am I having major anxiety over this. and the worst part is My doc said there is a change showing on the mri since the last mamo about 6 weeks ago. So not sure if this thing is on the move or it is just post biopsy stuff, doc is not sure either and she said she cannot say for sure what it is till it is removed and sent to the path.
The other worst part is I cannot have my green tea or coffee for 7 days before the sugury. I sure some of you have had a needle loc before if you have any support would be great I m terrified of surgury.
Hugs to all
Shirley
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excuse all of my typos lol
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oh forgot to add the slide were double cheked by another path dept
lcis
columnar cell change , fibroadenomatous change and apocrine metaplasia
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Hang in there, Shirley. We're all hoping it all comes out as something benign and uninteresting like fat necrosis. We're all reaching out our hand to you.
For the needle localization, you may want to have some sort of backup plan in case you do have pain. You may want to consider slathering your breast in Orajel about an hour before. Messy, but may help. You can wipe it off just before you go in. You may want to have a plan in place with the doc in case you do have pain. I had several hours between my needle insertion and my surgery (my surgeon was in a family emergency), so I'm glad I brought something to try to distract me.
I had no pain during the procedure once an anesthesiologist got involved.
Do whatever may calm you to get you through these days before the surgery. We're here whenever you want to vent.
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Thanks leaf , this whole things is making mentally sick uggg thanks for the input I hate pain too. I will let ya know how it go's i dont understand why they will not let me have coffee or tea seven day s before thats a killer. And thanks i hope it is nothing too.
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I don't know why they are ordering no tea or coffee x 7 days before (assuming you are fairly healthy otherwise.) I know the regulations differ from hospital to hospital, but this is quite stringent from my own personal experience and what I have read. (I assume you are not on anticoagulants such as warfarin (Coumadin) or have reflux problems,etc.) The standard I've heard is 'nothing by mouth after midnight', no aspirin or nonsteroidal antiinflammatories x 1-2 weeks before, stopping anticoagulants (such as warfarin, heparin).
There was no evidence to suggest a shortened fluid fast results in an increased risk of aspiration, regurgitation or related morbidity compared with the standard 'nil by mouth from midnight' fasting policy. Permitting patients to drink water preoperatively resulted in significantly lower gastric volumes. Clinicians should be encouraged to appraise this evidence for themselves and when necessary adjust any remaining standard fasting policies (nil-by-mouth from midnight) for patients that are not considered 'at-risk' during anaesthesia. http://www.ncbi.nlm.nih.gov/pubmed/14584013
Some of the surveys were asking about a breakfast of plain toast and tea 7 hours before surgery.
Gesh, maybe they're worried about A boy presented with the classic triads of acute onset altered mental state, respiratory depression and small pupils following consumption of a bottle of presumed "green tea", which was subsequently found to contain methadone.http://www.ncbi.nlm.nih.gov/pubmed/19347668
I'm sure you heard correctly, but maybe it would be good to call and ask another person (if you weren't told this by your anesthesiologist directly).
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caffeine (tea or coffee) can exacerbate fibrocystic breast disease, so they often discourage it for 5 days before mammos. I didn't have any restrictions before my lumpectomy, but that's the only explanation I can think of.
Anne
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Thank you well i went for pre op today ekg and blood work and mentioned about the coffee or green tea and she phoned my surgeon and she ok green tea said drink all I want but try to stay away from to much coffee. And said the no caffiene deal were orders from the hospitol. And she gave the ok for some vitamins, just wanted to know the brand. Now having major anxiety over this needle loc biopsy, Guess I am a big baby when it comes to being put to sleep it is a twilight sleep, not sure If I mentioned this before. With versed and propofol. Anyhow all of you ladies on here seem so strong and have been through this or worse I hope and pray I can be as strong. What else is scary is when they start asking you to bring your will power of att, I guess it is a standard procedure for any surgury. And thanks leaf you are so helpful
and supportive it really helps
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For me, propofol and versed (twilight anesthesia) were just fine. Every time I said 'Mmmmmm' (this was NOT from pain - I didn't experience any pain during the procedure - but more of a comment 'What's going on - where am I? - what are these sheets in front of my face?') I got another slug and was unconscious for ?15 minutes more.
Once an anesthesiologist got involved it was NO problem.
The problem for me was the needle localization-they didn't have an RN or anesthesiologist involved, and they were going in and out of the room,so they couldn't give any injectable anesthetic. (This may vary between hospitals!)
Of course I want you to have a pain-free and pleasant experience. What I would recommend: have a plan beforehand and BEFORE the needle localization starts, tell them you have pain concerns.
They told me just before the procedure, "You must promise not to move a muscle throughout the entire procedure." It felt like the needle localization lasted 1.5 hours, but I couldn't see the clock. I was a 'good girl' and knew if I told them I was in pain I would cry, and if I cried I would move. So I couldn't tell them I was in pain. They looked at my face, and they did give me another shot of lidocaine, which hurt as much as the wire insertion and didn't work. I did *not* get lidocaine beforehand. Some people do. The lidocaine either went to the wrong place or didn't work.
I hope I never have to have another, but if I have to do it again, I will bring bells or something to shake in case I have pain (and tell the doc beforehand) in case I don't feel I can talk. (Probably even shaking your keys would work.) If they don't respond, I'm not going to continue with the procedure, I'll pull out of the mammo machine, and walk out of the room, even if I have a wire inserted.
I did a poll here, and most people DO have a mild-moderate pain (<=5/10). Some do not. I was one of the people in the minority. I was diagnosed with a PTSD-like syndrome a few months after this procedure (I had pre-existing trauma too). On my next mammo breast biopsy a year later, I instinctively pulled out of the mammo machine (ouch!) when the radiologist tried to inject lidocaine (with a MUCH smaller needle than the previous doc.) He asked why, and I said 'because I am in pain.' They had to HOLD me in the mammo machine while I cried silently. Your body LEARNS from past experience.
I don't want this to happen to you. I was told by 'friends' that I should have just told them I was in pain. I wouldn't have been able to do that. I was having a pain score of at least 9. It was not 10 because my arm was not getting ripped off. My pain score would have been less had he ever asked if I was in pain. I was also concerned about my nudity (I work there!) because I kept on hearing the door open and close, and no one announced their name or position, and the door opened on a waiting room. People could enter, trying to find the restroom. I felt like I was 'on display'. I'm sure this didn't help my pain score. We all have different personalities.
Best wishes. Most people DO OK.
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Hi leaf, well I had the lumpectomy and boy they knocked me out when I woke up I was 2 of every nurse and they asked me to cough, it hurt like you know what! the nurse say oh you had a breathing tube in, I thought what ? Well I must have been so drugged I stop breathing. After they were able to get me off the oxygen and ready to go home, It was horrible I was vomiting all day and night. Anethesia is def not for me. And today my chest and back hurt. Did you have this happen to you? You were right the needle loc part was painfull I would say a 7 on the pain scale. The good thing is my dr said she got it all out so i meet post op with her on friday and we have results back from the path. And then a mamo on the right side in nov.
Whew i am glad that part is over and hope to never go through this again it was pure you know what.
Just wanted to let you know how it went.
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typo above I ment to say i was seeing 2 of every nurse seeing double
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I'm so sorry you had a bad time with anesthesia. I hope you never need any more surgery, but if you do, they can 'pre-med' you with anti-emetics. With my first general anesthesia, I threw up several times, but they've done a good job in my subsequent surgeries - haven't even felt nauseated. On my first surgery, even a week later, when I turned my head it felt the world was spinning around, yet I was able to walk 8 miles.
I didn't have any chest or back pain, but some people have a horrible time even with biopsies-lots of neck/back pain. So you are definitely not alone.
At least its behind you and I hope you never have to go through anything like this again!
Best wishes as you wait for your results.
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Thanks Leaf
went for post op visit and dx was atypical ductal hyperplasia and the lump was a fibroadenoma 1 cm and non atypical dh focAL Apocrine metaplasia.so great news! Still have lcis so need to follow up with onco for hormonal drugs, not sure which one tho scared to take tamox my mom had a stroke and her dad had a stroke and noticed risks with tamox is stroke. So will see on the 17 th what the onco has to offer to reduce risk, But thank god no rads needed. yippeee
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I am so glad you have 'nothing worse' than LCIS and ADH.
Some people with ADH choose to have their slides re-evaluated to make sure they don't have DCIS. (Of course, not everyone does. When I had my slides re-read at a major institution, it was $300 out of pocket for each biopsy, and they just sent 1 slide for each biopsy. This money was later re-imbursed to my by my insurance company. My diagnosis only changed from 'LCIS + some features of ALH' to 'LCIS with ALH'.)
If you are post-menopausal, there are other anti-hormonals. But its a discussion you will need to have with your onc.
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Yes thanks me too. Idid have my slides from the sterotatic double checked by a very reputable pathologist and hospitol was cedars siani in hollywood ca. i have a wonderful breast surgeon dr kristie funk you can google her. she did a perfect job. So it is just wathcing now with mamo in rt side in dec reg mamo in april and mri next year. I am pre menapausal, i really wish it would go away lol. They have mentioned tamox but with the high risk of stroke with the med kinda scares me since my mom had a stroke and her father died from a stroke it kinda runs on her side of the family.
I happy for you too sound like your is nothing much more than what i have also. Are you on and meds to reduce your risk?
Thanks
Leaf
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