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breast angiosarcoma



Total items found: 14

survivor9yrs
Posts: 6
Joined: Oct 2009
October 10, 2009 - 11:27am

i am a 9 yr. survivor of breast cancer. but in march i found a sm. lump with a blue bruise. i went to my surgeon and oncologist and was told it was a hematoma. here it is oct. and i have a secondary angiosarcoma. misdiagnosed..... this cancer is caused by radiation therapy. usually around 8-10 yrs. later... i have had a pet and ct scan, which were clear, except for the cancer on my breast. tues i see my oncologist to find out where i go fron here. this is a rare cancer, but with the increasing radiation for breast cancer, it will become less rare in time. for all of you going through BC and survivors, be aware of this. talk to your drs.

mlmjt1
Posts: 467
Joined: Jul 2009
October 10, 2009 - 11:32am

Just never stops does it? I just finished my chemo and still have herceptin to do for a year as well as reconstruction. I hope to be done with this stuff one day, but as I learned just know from a 9 year survivor you will have to be vigilent the rest of your life!! Sounds a little overwelming, but hey, we are surviving,right?

Hang in there

Linda T

survivor9yrs
Posts: 6
Joined: Oct 2009
October 10, 2009 - 12:13pm

thanks.. just want everyone to know about angiosarcoma. had someone labeled this when i had BC i would have opted for a double mastectomy... never would have had radiation. my BC was stage 1, had a lumpectomy and radiation. no chemo. this won't be the case now.. i have survived for 9 yrs. and i will be a survivor again..

VickiSam's picture
VickiSam
Posts: 616
Joined: Aug 2009
October 10, 2009 - 12:31pm

my surgeron has been trying to talk me out of my discussion. I knew in my heart that I was making the right decisioin.

I am so sorry about your second bc diagnosis. You are a strong women, and will get thru this latest fiasco. We are here for you, and I will be praying for you every step of the way.

VickiSam

survivor9yrs
Posts: 6
Joined: Oct 2009
October 10, 2009 - 4:24pm

vickisam
i wish i had gone the extra mile. i wouldn't be in this situation today. ask your dr. abt. angiosarcoma of the breast. it is a cancer of the blood vessels. caused by my radiation. i just had to post to all site i can find and let others know of this. thank you for your prayers. and i do hope all goes well with you.

survivor9yrs
Posts: 6
Joined: Oct 2009
October 10, 2009 - 4:20pm

i don't know where my head is at, but i wish you all the best in your fight against BC. Glad to know you have made it through chemo. that is something i am not looking forward to, but has to be with this cancer. good luck and prayers are sent your way.

BELIEVEx3
Posts: 22
Joined: May 2009
October 30, 2009 - 3:28pm

Hi I am a breast cancer, now angiosarcoma and thyroid cancer survivor........If you want to talk I am 3 years out from bilateral mastectomies for the angiosarcoma. I was given the gift of low grade AS and although I have had many surgeries I have not had a recurrence. I think the most difficult part for me was the lack of a support system. I felt to tell someone who was surviving breast cancer that I had this secondary cancer possibly from the treatment was too much for someone to bare..........I hope you are ok and if you want to talk, I am here.

survivor9yrs
Posts: 6
Joined: Oct 2009
November 7, 2009 - 2:04pm

well, in the past month i have been diagnosed, scaned (all clear) and had surgery. It's been a ride... had mastectomy and now will start chemo. taxotere and gemcidabine. surgery went well with great tumor to chest wall margins. just hope this will be it for this horrible cancer. so little information on it, makes it harder to know just what to expect. hanging in there. wonderful news, knowing some others have beat this cancer. I have heard of others too. stay well

mimivac's picture
mimivac
Posts: 1571
Joined: Dec 2008
October 30, 2009 - 3:36pm

So sorry to hear of your secondary cancer diagnosis. It just isn't fair that the treatment for breast cancer causes... cancer in the breast. It shouldn't be that way. I opted for a lumpectomy and radiation and hope I will not have to deal with the same. I wish you luck in your second journey with this beast.

Mimi

MAJW
Posts: 281
Joined: May 2009
October 30, 2009 - 4:11pm

To hear your news....but this may help......My sister in law is a 20 year survivor of angiosarcoma..I remember her being told it was a rare, rare breast cancer....and she had never had any type of radiation.......it came "out of the blue" They first removed the tumor and it took 3 months for a pathology report to "identify" it....remember this was 20 years ago.....She then had a mastectomy and no further treatment at all.....no chemo, no radiation. She's never had any kind of reccurence....

I know there are late term side effects of radiation especially leukemia, but I haven't heard about angiosarcoma being one of them.......yikes!
I am so very sorry you are having to go through this yet again....
I wish you the best.......

BELIEVEx3
Posts: 22
Joined: May 2009
October 30, 2009 - 6:24pm

Good to know someone is 20 years out from angiosarcoma..........I am doing well, and I hope to provide support to anyone out there who might experience this as well......

Tux's picture
Tux
Posts: 226
Joined: Aug 2009
October 30, 2009 - 8:43pm

Thanks for the info--yet another side effect to keep watching for. I am sorry that you are having to go through this again. Hugs & prayers sent your way....

survivorbc09's picture
survivorbc09
Posts: 1037
Joined: Jun 2009
October 30, 2009 - 11:30pm

I have never heard of this, but obviously, rads don't always cause it, if at all?

BELIEVEx3
Posts: 22
Joined: May 2009
October 31, 2009 - 1:27pm

Hi I tried to post earlier...........AS can be a primary or secondary cancer, although very rare. Current literature does show a correlation between a previously irradiated field, the dose of radiation received and the rare occurrence of AS, is it the cause, maybe in some cases. AS is one of the secondary cancers the doctors speak of as a risk of our treatment....Remember very rare!!!!!!!Please do not worry, the key is to know your body, keep vigilant with your follow-up and if something persists speak with your oncologist.

BELIEVEx3
Posts: 22
Joined: May 2009
November 6, 2009 - 4:42pm

Sorry about the duplicate.