Anyone dealing with Atypical Ductal Hyperplasia (ADH)?
I am sorry if this is not the right forum. I know ADH is not cancer and this is a breast cancer forum, but I can't find another forum that may be more relevant.
I am wondering if there is anyone who is dealing with ADH or has been diagnosed with ADH that can share their experience. I was diagnosed a month ago. While I am relieved that I don't have cancer, I am confused with the radiology report that shows BI-RAD6 - surgical removal is recommended. I have seen a breast oncology surgeon and I don't think she took me seriously because I don't have cancer. It almost feels like I wasted her time seeing her because I don't have cancer. If ADH is no big deal, why BI-RAD 6 (which i understand is for biopsy proven malignancy). I also read up about ADH online and understand that with ADH, my risk for breast cancer is 4x. Should I not worry about it and just do annual check? Should i see another breast surgeon? Should I see an oncologist? Do I need genetic testing to better understand my risk? I feel like an impostor for even posting this on a breast cancer forum but I am genuinely confused and concerned. Any help will be greatly appreciated.
Interested in more discussions like this? Go to the Breast Cancer Support Group.
Biopsy and lumpectomy were fine. They did not find anything further in the lumpectomy luckily
I only took day of surgery off. But I have a desk job.
I just recently had a breast cancer dx in the same location I had ADH excised 8 years ago. That puts me in the 15 percent of women who go on to have breast cancer. The pure mucinous cancer (2% of all breast cancers) was found on a diagnostic mammogram that happened only because I had read that inflammatory autoimmune disease increases your risk. I asked for my risk to be newly calculated (protocols have evolved but no one advised this) and moved on to advanced screening -diagnostic mammo, ultrasound and mri. My cancer was likely missed on yearly mammos as it is slow growing and I never missed one. I'm sharing not to scare anyone but rather to encourage people tp advocate for themselves when they have questions and concerns.
I was diagnosed last year with atypical ductal hyperplasia had breast excisional biopsy done. However, after that there is no follow up every 6 months and no medication given. Wonder if the right path is to follow or should I get a second opinion. I'm just concerned because I have read a lot about it, and I see that it is recommended to take medication for 5 years. I would appreciate any advice thank you.
Hoping the biopsy went well and you have gotten good news on the pathology!
Hi @debbie2721 thank you for sharing this, it is important information. Just for my own edification, can you post a link where I can go read the article, I am very interested in this.🤓
https://www.ncbi.nlm.nih.gov/books/NBK470258/
I hope this helps.
So based on your ADH you were not put on additional screening via a high risk breast center?
I am in the Seattle area with Fred Hutch etc (so major cancer center), but 8 years ago protocol only involved diagnostic mammograms for several years and then I was moved to yearly standard mammograms. Protocol has since changed and with ADH now I would have been given a baseline breast MRI and followed more closely. I asked for a review of protocols this past January and a diagnostic mammogram and MRI were scheduled for March. My cancer was found at that time.
Wow I didn’t realize the protocol had changed hope all is well