DCIS - Hip pain?
Boy, it's been awhile. Had a lumpectomy w/rads in 07 for grade 3 dcis. About a month ago developed deep hip pain. Got a pres. for Meloxicam from family practice Dr. for arthritis. I diagnosed myself because I'm so smart. No relief after a month and pain continues for no apparent reason. No exercise or anything different. Question: I know bone mets can sometimes be a result of breast primary tumor. Does this apply also to DCIS? What a moron I am, not to mention wus.
Thank you for your time.
Comments
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Don't know but have you considered it might be something like sciatica? I have bouts of what I think are that which I have linked to standing funny or, right now, being tense on the rad table and sleeping while tensing my body wrong. When I figured out what was probably happening, I was able to "untense" and it has gone away.
Still, as hard as it is, I think you need to see your doctor.
Many hugs..................keep us posted.
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You cannot get bone mets from DCIS. DCIS is non-invasive. Only invasive cancer metastasizes to bones, or anywhere else. So if you only had (and have ) DCIS, you can't have bone mets. If you're anxious, mention this to the doctor. But I think it's important to remember that our bodies are still subject to the normal aches, pains, illnesses, etc. of life. It's natural that we read everything in terms of DCIS, but not everything is DCIS related. For example, I got really woozy yesterday. If I had been in the middle of my radiation treatment, I would have thought it was a side-effect of radiation. The only problem is, I haven't started radiation yet. Woke up this morning with a stomach virus, which is not fun at all, but probably explains yesterday's wooziness and is clearly unrelated to my DCIS.
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Regretably while DCIS is non-invasive, people who have had a diagnois of DCIS can develop invasive cancer and I think that is what austin2k3 is worried about. Austin2k3 also seems to have grade 3 DCIS--same as me. I was told that was the type of DCIS that was most likely to develop into an invasive cancer. While my brain won't jump straight to bone mets [hopefully] when I am done with my treatment, I will still keep in close contact with my oncologist and if there is something funny those first 5 years, you can bet I won't waste time in getting in to see a doctor.
No, we shouldn't go through life thinking every owie is a new type of cancer but nor should we be complacient [sp] about having been diagnoised and treated with breast cancer. It changes life and it changes you. We can't ignore that. Example, I was a life long organ donor, since I was 16. Some one on the boards just said that with a diagnois of cancer, you can't be an organ donor or even donate blood. Whoa. It may not be true, I have to investigate more but that was the biggest slap in the face from this stupidbreastcancer in a long time. As my husband put it, as an organ donor, you might be dying but some kid will get a kidney and live, some burn victim will get skin and heal, some person will get a cornea and see. And Now I find I'm nothing more than compost. That really hurts.
Sorry to digress. Point being, austin2k3, you need to talk to your doctor if for nothing more than your own peace of mind.
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Austin2k3:
Please listen to 3monstmama: For your own peace of mind, go to your doctor! I had my surgery 2 years ago, and the first year I had every ache and pain imaginable-- my oncologist didn't take my concerns very seriously-- stress, anxiety, and middle-age, she kept insisting (and she was right-- but that doesn't mean my cancer will never come back or be invasive when it does). Fortunately, my GP said, "hey, why worry?"-- and when I said I have a pain in my rib, which lasted 3months, she sent me for an ultrasound and then a CT scan. Of course, we don't want to overdo tests which have radiation risks, but I was convinced I had bone mets. Now 2 years later I do have lower back pain-- yes, I'm 45, but I never had it before-- but it is positional, so I'm learning to tell what is a red flag and what is part ofthe aging process. The point is, don't hesitate to insist on getting things checked-- it's scarier not to know then to get to the source of any pain.-- Please keep us posted on what happens.-- Julie
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good advice from everyone - 99% not cancer, but get it checked for your peace of mind.
and 3monstmama - I was taken aback by that posting too - re organ and blood donation. With regards to being something not just compost. In my area - NYS Capital District - a local hospital, Albany Medical Center has a very popular anatomical gift program in which the deceased are used by medical students. Every year, there is a service at which the medical students express their appreciation for the people who donated their bodies so that they could learn to be doctors. My mom, who died of lung cancer, donated her body and I was amazed at the number of people who attended that year's memorial service and how very moving it was. I don't know if you have such a program in your area. It is something to consider if indeed organ donation isn't doable.
Julie E
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I had deep, intense pain in my left hip for about 2 months this spring. The pain would wake me in the middle of the night, crying.
Onc was useless - mentioned it at checkup.Saw an orthopedist who specializes in knees, hips, and ankles. She offered me a CT scan immediately, but said that since the pain was in the joint, rather than in random place in bone, that it was more likely to be bursitis, brought on by my bad knee, which had flared up while DH was undergoing treatment for esophageal cancer, so I hadn't paid any attention. NSAIDs (lots), ice on both knee and hip, brace and cortisone injection for the knee. Within a week, the hip pain was gone.
And I spared myself that "radiation from 30 X-rays" that a CT scan equals.
Personally, I was terrified, and am so glad it's over.
If my orthopedist weren't married with a couple of kids, I would adopt her. Best doc ever.
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This is somewhat related...
can anyone explain why someone dianosed with stage IIIb, no node involvement and has metastasizes? How can cells travel through the body and not make 'deposits' in the nodes?Thanks.
-c -
Thank you, sisters. I'm sorry you're all here but what a great group. Dr's appt. this afternoon. God bless you all.
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iHEARTu-
I have noticed the number of women whose personal info shows stages III and IV with no node involvement too. I think this is because the cancer cells don't only travel through the lymph system, they can also travel through the blood system. I think the nodes provide parking areas for cells - and maybe if cancer cells are traveling in the lymph system - they will congregate in the nodes. I don't think the venous/arterial system has comparable points. Perhaps someone with medical knowledge can chime in here. I am glad this came up on the DCIS board.
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iHEARTu,
Anyone with invasive cancer faces the risk of mets, even if they are node negative. DCIS cancer cells are confined to the milk ducts, so they can't enter the lymphatic systemic or the vascular system and travel into the body. But invasive cancer cells are sitting in open breast tissue and can move around anywhere. Most often, if an invasive cell leaves the breast, it travels out through the lymph nodes. That's why everyone with invasive cancer, even just a microinvasion, gets their nodes checked. But if only a few cells went through the sentinel node (the first node in the string of nodes), it's possible that they may have gone through undetected, i.e. without leaving any cancer cells behind to be found. Cancer cells can also travel outside of the breast through the bloodstream.
According to Dr. Susan Love, in approx. 20% - 30% of cases where women are diagnosed with node negative invasive cancer, in fact a few cancer cells have made it outside of the breast prior to surgery. This risk increases as the tumor size increases and is higher for those who have more aggressive tumors (grade 3, HER2+, for example). And all this gets to why even node negative women who have invasive cancer are often given chemo and prescribed Tamoxifen or an AI. If the size of the invasive tumor is small (generally considered to be less than 1cm in size), then usually the risk is judged to be low enough that chemo won't be prescribed, unless the cancer is particularly aggressive. Tumors between 1cm and 2cm are sort of in the grey zone - sometimes chemo will be prescribed and sometimes it won't be. But certainly once a tumor is 2cm in size, chemo and hormone therapy will almost alway be recommended, even though the nodes test negative.
I hope my explanation makes sense.
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Sorry you have so much pain. I too have had severe hip pain since my 6 1/2 week radiation treatments end of April thru Mid June '09. I had an MRI and two compressed disks were found. Doctors seem to think it sciatic nerve pain. I am currently doing acupuncture, massage and chiro treatments...starting to help. The pain is excrutiating down on both sides of my leg (right). I think radiation really is a double edge-sword. It fixes one thing, and stirs up other things. I say this because in addition to 'sciatic' pain and extreme fatigue, Drs. have found elevated levels in my RA autoimmune panel.
More than likely rad tx's triggered this. Go to your doctor and check your pain out...it's worth the peace of mind. As a cancer survivor you need to be positive about anything that comes your way....so listen to your instincts! Much Hope your way!
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