How was your DCIS found? What grade?
Hi,
Just wondering for my own curiosity’s sake.
Back in December 2015 I went to my internist for a skin tag removal referral and some irritable bowel symptoms and she suggested I get a mammogram since I was past 40. She didn’t agree with the new guidelines of 45-50 and thought all women needed a baseline at 40 based on her experience. And there the BC journey began. . . even when I was called back for another “diagnostic” mammogram on the left, I didn’t think it would be anything serious.
I feel so grateful that I dodged a bullet some days. I could be walking around with DCIS that could have eventually turned invasive had I not gone to have the mammogram last Dec. since it was labeled high grade. Then again, I could still be walking around in blissful ignorance. . .
Anyway, wondering how your DCIS was found, it seems mammogram screening is the only way and women should get it at 40 not later. Kind of an informal survey. . . even if it is statistically correct to start at 45 I think they should have women start at 40 since I’m hearing so many younger women are affected and it tends to be more aggressive in younger women.
Thanks!
Night Owl but trying not to be
Comments
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My stage 0, grade 3 DCIS was found by mammogram when I was 52. In the other breast, the stage 0, lower grade DCIS (plus IDC) was found by the MRI following the mammogram, which did not show it.Nothing was palpable. I've done breast self-exams since I was a teen and had a mammogram annually from 40-52.
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Mine was found by annual screening mammogram at age 59. Grade 3.
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Mine was found by a screening mammogram at age 45. I had gone for them at 40 and 41 but when the new recommendations came out, figured I was ok waiting for a while. My mother was diagnosed when I was 45 which made me second guess that decision and go in. I was diagnosed 6 weeks after she was.
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Strong family history has led to yearly mammos since I was 30. (Gma had BC at 35, 45 and 84, mom at 42 and 50, her sister at 32 and 34). Mammos and ultrasounds last June showed water-based cysts and possible calcifications, which led to a 6-mo 'watch and wait' follow-up in Jan. Following the Jan mammo and ultrasound, I was sent to MRI, followed by MRI with biopsy and marker placement. Diagnosed with moderate grade DCIS, cribriform-type at age 43. Feeling like there should be an award for enduring 4 mammograms in less than a year.
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Had a lumpectomy for a palpable left breast lump at age 35, it was benign - annual mammograms thereafter with many callbacks. When the gov't recommendation came out approving a mammo every couple years I took as a pass for the annual mammo afterall those tech's didn't know what they were doing, that's why I had to always return for a 2nd (LOL!). After a few yrs off mammo went back age 47 and dx. Coming up on 4 years within a month. Felt like it was yesterday. Final path after bmx found all sorts of bilater lobular ALH and LCIS not detected by pre-op MRI.
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Hi,
I thank all of you ladies for responding! I am happy you are in so many different parts of this cancer journey and well. I was royally pissed off the first couple of months, but have pretty much accepted this diagnosis. Just trying to be grateful daily! And I’m telling all my peers/mom friends who are in their early 40s to get screened and push for it even if their docs say the new guidelines don’t indicate it is necessary.
I still have my good boob to worry about, I’ll just live one day at a time and get screened regularly for that one. . .
Thank you,
Night Owl
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I was diagnosed after my first mammogram at 42 -- I put it off for a couple of years until my friend was diagnosed. When they call you back before you get home, you know that something's amiss.
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I was diagnosed after a lumpectomy for an intraductal papilloma. I'm 38 and was diagnosed on March 17 with high grade micro papillary DCIS. There was no lump and nothing was seen on mammogram. I had bloody nipple discharge which sent me to the doctor who sent me for a mammo. They then did a ductography which showed a dilated duct and a papilloma. Surprise, after the lumpectomy for the "papilloma" it turned out to beDCIS.
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I was diagnosed after a lumpectomy for an intraductal papilloma. I'm 38 and was diagnosed on March 17 with high grade micro papillary DCIS. There was no lump and nothing was seen on mammogram. I had bloody nipple discharge which sent me to the doctor who sent me for a mammo. They then did a ductography which showed a dilated duct and a papilloma. Surprise, after the lumpectomy for the "papilloma" it turned out to beDCIS.
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I just turned 43 and was just diagnosised yesterday. I found a small lump and went for a mammogram and ultrasound. Turns out the lump is nothing and the DCIS was just under in. Have lots of mixed emotions
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Dear sunflower215, Welcome to the community. We are so glad that you reached out here and we hope that you will stay connected, and find others who will offer support and information. Please let us know your questions and concerns and use these discussion boards to help you to navigate as you continue. The Mods
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Mine was found during my regular yearly mammogram. I had been to my gyno the previous week and he didn't find it. Mine was grade 3. My lumpectomy found a small portion of IDC, grade 2 that was HER2+.
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Thank you Deaconlady, Sunflower21, Loveotters, and LAStar for responding.
It just makes the case for mammogram screening earlier than the new guidelines. I wonder if there will be changes again. I hope so. Regardless I am on a personal campaign to tell all my friends to get screened since DCIS is usually not-palpable. It seems most of the time the palpable tumors have turned invasive. I think the folks making the guidelines are looking at survival rates. Well yeah, BC is treatable, but if women can get screened before it turns invasive they are saved from chemo/radiation right?
Take care everyone and thanks for responding.
Best,
Night Owl
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Thank you. Have lots of questions and very confused ☹️ Some people say it is just DCIS no big deal. Um I think it is a huge deal. Hoping that hearing other people's stories and asking questions will help me.
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Hello everyone,
My DCIS was diagnosed in my yearly mammogram. Stage 0, medium to high grade with a micro-invasion. I have had mammograms yearly since turning 40. I feel very lucky to have caught this at such an early stage. I have no family history and my BRCA was negative. I tell my story to anyone who will listen, yearly screening is so important.
Best of luck to everyone on this horrific journey...
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When they removed the 1.5 cm IDC tumor during the first lumpectomy they alsofound the following: "DCIS, multifocal, solid architecture, nuclear grade 3, central necrosis." No one explained what that meant exactly, but I had to have two extra surgeries because of close margins with DCIS.
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Mine was found when I had a prophylactic double mastectomy as a result of being BRCA2+.
Less than a year before I had a breast MRI. 4 months before I had a diagnostic mammogram.
Take care
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Routine mammogram at 57 - watch and wait for 6 months and then the diagnosis. Grade 2 and 3, no necrosis (thank goodness) I think a baseline should be done at age 35 (the old guideline) and then yearly after age 40. Period. No way should people wait to 45-50!
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Mine was found with an MRI it was Grade 3 - I had a clear annual digital mamo just the a few weeks prior to the MRI (and for about 6 years before all mamo's were clear) but it was suggested by my daughter's doc that I have genetic testing (family history) which included an MRI... don't be fooled - My DCIS was not seen by a mamo! IF you have family history my genetic counselor suggests that an MRI is the way to go.. It all depends on who reads it of course but I had another mamo done in another facility just to check and they did not find DCIS at all . So in my case it could only be seen by the MRI. I had the pathology lab send the slides to another facility (after the biopsy) out of state and they found DCIS grade 2/3. Doesn't hurt to have many eyes on everything IMO... Best of luck - I hope you recover and feel good about your decisions!!! Deirdre
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Rountine mammogram. I really had no concerns because there is no family history. Apparently Ijust changed my family history.
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Mine was also found during a routine mammography at age 66. Grade 3 ER and PR + > 95%.
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Hello,
My 50 yo mom had clear and bloody discharge from her left breast, and went in for a mammogram, then a 3D ultrasound, but nothing was seen until she had an MRI. They saw 3 2cm masses, and performed a biopsy that came back with secretory-like findings. Originally, her doctor said it was stage 1, grade 2 and triple neg. He said she had a very good outlook and wouldn't need chemo or radiation, only a lumpectomy. Then he came back and said she would need chemo, and came back again 2 weeks later saying she wouldn't. She just had a double mastectomy 2 days ago. After the surgery, her surgeon came out and said they got all of the cancer and that her outlook with secretory was good. The pathology report just came back today saying that she had 2 tumors in the left breast. One was 0.6 cm and the other was 6 cm. The report says the pathologist found DCIS, cribriform and micro papillary, and secretory types. It also says she is stage 3, and her doctor says she will need radiation or chemo. What I don't understand is how 5 months ago there was nothing on a mammogram, she only had 2 cm masses, was stage 1, and wasn't going to need chemo. Now she has a 6 cm mass, is stage 3 and probably needs chemo. How could they have missed a 6 cm mass? How did it take her doctors 5 months to figure out what was wrong with her? I feel like they have no idea what they are doing, and I need to find her a doctor that has treated invasive secretory carcinoma before. I'll take her anywhere. I don't care if we have to travel to the other side of the country. Any suggestions?
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hello....mine was found with annual mammogram checkup. Diagnosed Nov.2015, also brca1 ,est+.
It wAs first diagnosed DCIS 2.0 cm, grade 3iin right breast, scheduled for surgery February 8. By the time I had
Full double mastectomy with reconstruction,,I had already developed more DCIS 2.5 cm, grade 3 in my
Left breast. .
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i believe my doctor saved my life. She insisted that she preferred a baseline at 40, even though the false positive rate is high. So I went. 3 weeks later I had cancer. I had just turned 40.
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As much as I hate that we have these stories to tell I love having people who can relate to our experiences.
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I did my routine checkup every 2 years. 2014 was the year I was going to skip my exam. Right before Thanksgiving I rubbed against a chair and felt a pain on my breast and saw it was red and warm to the touch. The next day I went to my doctors office and asked for an appointment and was seen the next day. My doctor was going to aspirate I think that's what she called it but didn't feel comfortable with what she saw. She sent me to a surgeon across the street and that is when it all started. I had some form of infection which caused my breast to look red. After a couple of weeks of antibiotics and no change the surgeon said that he had to surgically remove the mass that was there. What they removed wasn't cancer but what they found next to it was. After mammogram. US, biopsy I had DCIS, Stage 0, Grade 2. I underwent 5 weeks of radiation on my right breast. I just recently had my left breast show signs of DCIS. I have to now see my surgeon this coming week and I hope everything is ok and that results will be negative. I am also telling everyone to do their mammogram every year or every other year, but not to sleep on it because all the years that I had previously had my exams nothing showed up until 2014.
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I was 55 years old last year when I went in for my annual mammogram. I opted for the 3 D Digital mammogram and M so thankful I did. I received a call back for diagnostic mammogram and ultrasound. The core needle biopsy came back with benign findings but the pathologist and radiologist determined the results were discordant. I had n excisional biopsy in May of last year that revealed DCIS, grade 2 as well as LCIS.
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I spent a year having pain, skin changes, and hot/itching sensation after a breast aug. My plastic surgeon kept saying I was just healing slow on that side. I finally went to my PCP and asked for a mammo, which found microcalc cluster. We couldn't get a needle biopsy because the implants were in the way (tried 2x under a mammo press to get the needle in... that was FUN! Not.) An excisional biopsy found high grade DCIS. I had to fight with the surgeon to even do the biopsy... he insisted it was not going to be cancer, and he kept finding ways to put it off for three months.
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Funny you ask this, because my story is much like yours. At the dr Office for something else (random) and she said, "Oh, by the way...you are 39 and due for a physical in a few months, want me to order your mammogram now?" This began my journey. I was dx'ed w atypical lobular hyperplasia and had a lumpectomy. Pathology returned with DCIS (Stage 0)so I then had a bi-lateral mastectomy with reconstruction on March 31, 2016. I am SO glad I had a mammogram when I did!
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I've been fairly good about getting annual mammograms probably since 40, although my mom did have something that was probably DCIS--she had a mastectomy at 62 but is still doing great at 87 and has had no recurrence. (One doctor told her several years later that had it been diagnosed then, she would have had a lumpectomy vs. mastectormy.) I had ALH with lumpectomy seven years ago. Was a little late getting my regular gyn exam/mammo this past time, but had the same microcalcifications on the one in February that they saw the last time. FWIW, DCIS is not something that can be felt (or seen during surgery). Yes it's non-invasive, Stage 0, but my BS calls it "squirrely." I'm 58.
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