Waiting for surgery - lumpectomy. Scared of what lies ahead.
I'll be 76 in three weeks. I'm very healthy and don't take one pill for anything. But, two weeks ago, I discovereda lump and immediately went into sheer panic. Needle biopsy confirms malignant, non-invasive. However, my surgeon feels that it might be invasive. She said most lumps we find ourself are invasive. My husband died seven months ago, and although I have support of family and friends, I feel very alone. I'm now wondering about the other tests after surgery. Do they do a PET, CT scan, bone density? I never expected to take this journey. However, I have many close friends who are survivors. Hope the same will be true for me.
Comments
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What does your physician recommend for follow up testing? You may find this section helpful, as it discusses diagnosis and testing. Testing. We are all here for you, regardless of what they discover. We are sorry for what you are going through, and sincerely sorry for the loss of your husband.
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Hi Cathytoo .. so sorry about your diagnosis and the loss of your husband. That is so much all at once. But you have come to the right place and are not alone here. I wish I had found these boards sooner. I am no expert, but just wanted to tell you that after my biopsies, I was sent for a CT and bone scan. I'm not sure if that's the general rule everywhere. I hope that more ladies can come along and give you better information. Hang in there and remember to take deep breaths. This helps.
Edited for typo..
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Cathy,
Different areas, hospitals, have there own set of protocols. I did have a PET scan,( after my lumpectomy ) but was told it was because of all the node involvement & extranodal extension.
All those scans are very expensive, and if the Cancer has not traveled to your axillary nodes, not necessary. A dexa scan to measure bone density is common for women over 60, with or without BC.
Get the surgery scheduled, the waiting part is the worst.
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Got to say .. I agree the scans are expensive and many times not necessary. In my case, this caused more stress for me and nothing else was found, either. I can see their point AFTER my surgery during which they found a lymph node involved, but not before. I believe the medical system getting to be out of control .. and because I have medicare and also a supplemental health plan to cover what medicare doesn't, they saw dollar signs. But that's just my personal opinion and a whole different subject! I would say, I was too upset to question anything at the time. I hadn't found these boards, either, so didn't really know what to question. ;-)
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Hi Cathytoo:
It sounds like the biopsy showed "malignant, non-invasive" disease so far. That sounds like some sort of "in situ" disease, still confined to the inside of the ducts (non-invasive), such as "ductal carcinoma in situ" ("DCIS")? Purely non-invasive disease has a very favorable prognosis.
As you have learned from your surgeon, there will be additional pathology done on the tissue removed by lumpectomy which might find additional disease (more extensive non-invasive disease) and/or possibly invasive disease. For example, invasive disease is found after surgery in roughly 20% of DCIS cases. Again, "non-invasive" indicates very early stage disease (Stage 0) so far.
Some local practices differ, so you may see some earlier stage patients receiving PET or CT scans. However, even if invasive disease is found, please note that many Stage I and II patients do not receive PET or CT scans in the absence of clinical symptoms of metastatic disease, and current consensus guidelines for clinical stage I-IIB disease indicate such additional studies be considered only if directed by signs or symptoms. See e.g.,
http://www.medscape.com/viewarticle/836945#vp_2
In case the above link requires registration (which is free), you can just google the title of the article to access it without registration:
Title: Imaging for Distant Metastases in Early-stage Breast Cancer
See also, Item #3 in this document:
http://jco.ascopubs.org/content/30/14/1715.long
For now, try and take things one step at a time. Being very healthy will be an advantage to you in recovering from surgery and any other possible treatment.
BarredOwl
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Cathy,
Just checking in to see how you're doing...we're all thinking of you!
--The Mods
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Hi Cathy,
I'm still a newbie to this site to some extent so am no expert. However, it sounds like you have a similar diagnosis as mine---DCIS. Which is all I know about so far. It's a journey of leaning and understanding more and more along each step of the way. I'm a nurse, but I knew little about breast cancer and current treatments, etc. so there was a lot to learn about.
I'm sorry for the recent loss of your husband but glad to hear you have some family support. Even though DCIS is an early stage cancer, receiving that diagnosis is still difficult. Or it was for me. My 80 year old mother had been diagnosed with stage 2 IBC just weeks earlier, so that compounded my anxiety even more. She and I support one another and we have the support of our entire family. But even with family support, it's still an alone feeling. My mom and I are probably our biggest supports for one another because we can share first hand how it really feels.
What is your treatment plan since your diagnosis? Any additional tests? Surgery? After stereotactic bx conformed my diagnosis, I had MRI and then 2 MRI biopsies which were negative. I'm 6 days post lumpectomy and see my surgeon tomorrow for follow up appointment and then will move on to the next step.
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