bone scan question
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anna313
Member Posts: 2
I had great news, no mets on bone scan. Curious, what does
"Nonspecific parenchymal uptake seen in both breasts, left greater than right". I've checked the usual sources. Anyone know?
"Nonspecific parenchymal uptake seen in both breasts, left greater than right". I've checked the usual sources. Anyone know?
Comments
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I think it just means that your breasts took up the tracer...sounds like they don't know why either. Congrats on the clean scan!!!! Best wishes!
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Last week, my onc. told me that my red blood cell count was very low. Will do another blood text next week, and he asked me if I am willing to have a bone biopsy. Has anyone had this done?
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I haven't had one done, but my onc wants to do one in September if my counts are still low. Many people have told me they are not painful--but I'm not too sure. I would prefer to be in a twilight sleep or something during the procedure, but I think my onc just does them in her office. Since you're the first person I know with bc who is perhaps having this done, I'm very curious what your counts were. Is it just your red blood cell count that is low? Are your hg and hemocrit also low? Is your onc concerned that you could have mds (myelodysplastic syndrome)? When did you finish chemo? Sorry for all the questions, but I've been so concerned ever since my onc mentioned mds to me as a reason for my chronically low counts, fatigue, and frequent infections.
Good Luck,
Connie -
Connie, having had a bone scan in the past, all i can say is that it is totally noninvasive. You lay still and the instrument just kind of goes over you like a wand. I had the technician sit with me through the procedure and we talked - the 20 minutes went super quick. it you're super anxious talk to your onc about a small dose sedative if you think you'll need it, but really it was a piece of cake- especially compared to everything else. So though i can't answer any of your questions about blood counts etc, hopefully i can help put your mind at ease regarding the procedure itself. Good Luck
LittleFlower -
Little Flower,
You sure it doesn't hurt? I saw pictures of someone having it done (the pretty young women who writes for some fashion mag and who has leukemia or perhaps non-hodgkins lymphoma?) and it looked really painful...I hated c-sections or rather being sedated for them with spinals.
Anyway, thanks for the reassurance. Why did you have them done?
Connie -
I think you are referring to a bone marrow biopsy. My onc also mentioned I may need to have this checked due to low red blood counts six months out of chemo (which he felt is unusual). That said, sometimes I think it just takes months for the side effects from chemo to disappear. My dizziness related to the low red blood count has seemed to improve recently, so I am hoping for good news when I get my bloodwork in two weeks and see my onc. I have noticed other side effects such as fatigue and vision problems that I have had are slowly improving also. I am now 7 1/2 months out of chemo, 5 1/2 months out of radiation. I think chemo is just the gift that keeps on giving!!
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Ah, Sue, you are exactly right! Pardon my not reading LittleFlower's reply very well...I've had bone scans and they don't hurt at all. And yes, I am referring to a bone biopsy as Jrp1 mentioned...
My onc wasn't worried about the low counts until this March. I finished chemo in Dec.2005 and rads in April of 06. My counts never went up and actually get a little lower. Also from my limited knowledge of counts, other things in the bloodwork seem out of whack,suggesting large, immature cells. But I'm not neutropenic yet. And I'm just slightly anemic. Sue, how low are your rbc--and you're right, you are so soon out of chemo, you're probably still just recovering. My other doctors (rad onc, internist) feel that my counts should be higher by now and that the low counts explain the frequent infections and chronic fatigue. My med onc thinks I should wait until Sept to do the biopsy. Is a bone marrow biopsy the same as a bone biopsy?
Thanks again for catching my error--I've never recovered from chemo-brain.... -
Bone scan, Nuke Bone Scan, Bone Biopsy, X-rays, MRI, Cat Scans, Nuke Heart Tests, Blood Tests, Mammograms, Digital Mammograms, the endless pictures, biopsies, and pathology reports.
Few doctors are trained to read exrays or perform bloodtests, pathology tests, etc. It's all done in the dark secret rooms hidden away in Wizard's labs with magic wands and giant magnifying glasses. lol. kidding
The specialists who read and write the reports are the actual diagnostic experts; what if they happen to be tired, have a bad day, are in a hurry, or even pass the job off to a med student? I find it all mysterious and somehow feel jipped because the physicians rarely even see the real thing. The techs are often students, and I can't tell you how often they flub things.
Phlebotomists only need a year or two of training; my arm can testify to that one! I had some scarey mishaps with trainee techs, nurses, docs, and I went to an excellent hospital with exceptional insurance.
Chemobrain is so bad, I don't even leave the house; only for short errands, dog walks, and doctor appts. Last time I went to the surgeon for 6 wk follow-up, a policeman came up to me in the grocery store and asked me if I had been drinking or doing drugs! I was so embarrassed, decided never to go shopping again. Had to tell him I had chemo, rads, breast cancer and peripheral neuropathy; can barely button shirts, turn pages, and stumble a bit; have a hard time with dizzy spells. Docs say, it will go away, eventually, maybe. Maybe?
It's not too bad; it's not too good. Limboland is strange.
Indi
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