Skip to content
Forum IndexCommunity Member List → Profile for mustanggirl

mustanggirl

Kenny_s_cobra_006

Member Since: September 1, 2008
Last Login: October 18, 2008
Location: Naoma, Wv United States
Occupation: Secretary

Biography

Diagnosis

Recent Posts by mustanggirl

Posted in: Not Diagnosed but Concerned + Waiting for Test Results, Created: Oct 18, 2008 08:08 am

Help me understand, please

I finally got my path report back.  Happy to say no cancer was found.  There were some items noted in the path report regarding changes.  My surgeon did go over the results with me and said no cancer, but I still don't feel comfortable with the changes listed.  Just trying to be as informed as I can incase I have to go through this again later. 

The tumor itself was a fibroadema with foci of apical proliferation of epithelial cells.  The stromal tissue is markedly hyalinized and increased cellularity is seen in the perductular stromal tissue.

The extra breast tissue that he took out showed irregularly dilated ductal structures of various sizes in fibrofatty tissue stroma.  Small ductual structures exhibit foci of dystrophic calcification.  Fibrocystic change, nonproliferative / dystrophic calcifiction, focal

Thank you. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Oct 2, 2008 10:44 pm

Surgery Tuesday/Questions

I have a questions for anyone else that has had this procedure.  It has been a little over a week since I had it done and I have started to have a bloody discharge from my nipple.  The tumor was behind my nipple.  Is it normal to have this?  I thought if something like this was going to happen it would have happened sooner.  I did not have any kind of discharge before now, it looks like only blood that's coming out. 

Thanks for any insight.

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Oct 2, 2008 06:27 pm

Surgery Tuesday/Questions

Yes it was.

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 24, 2008 12:46 pm

Surgery Tuesday/Questions

Thought I'd let everyone know the tumor was B9.  He said it was a fibroademanoma.  Then he went on to say that he took out some other tissue in the same location and was sending it off for a better look.  He did say he thought his diagnosis would not change, but better to be sure.  I'm glad to know he's leaving no stone unturned. 

Thank you to everyone for listening and all the advice I've received over this last month. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 18, 2008 09:29 pm

Surgery Tuesday/Questions

I saw a surgeon today.  He scheduled me for outpatient surgery on Tuesday.  First I have to go and get a wire placed because the lump cannot be felt.  Then to the outpatient dept. where he said he's taking the whole thing out and a good circumference of surrounding material.  Then he's sending it to pathology to get a result before he closes. 

He also started talking about options in case it come back cancer. (do they usually discuss this at this point?)

Please let me know what to expect from here.  I'd appreciate any info you guys can provide.  Thanks for your time.

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 17, 2008 10:15 am

Wait 6 mo. or biopsy?

I had the same thing happen to me....I see a surgeon tomorrow.  I'm not waiting "to see if it grows in 6 months".  (that's what the radiologist said to me)

Try not to worry.  I know that's easier said than done. We've all been there or are currently there.  I've found support and positive energy here I hope you do the same.

Good Luck.  My thoughts are with you. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 14, 2008 10:17 pm

Thyroid & Breast Cancer

WishIWere 

Here is the web address for the article again.

http://seniorhealth.about.com/library/weekly/aa092400a.htm

I copied and pasted it off my computer.  Hopefully you can get into it with this link.

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 14, 2008 06:46 pm

Thyroid & Breast Cancer

Here are the web addresses for the three I was looking at before I posted my question.

thyroid-info.com/articles/breast-cancer.htm

women.webmd.com/news/20030410/underactive-thyroid-lowers-breast-cancer

seniorhealth.about.com/library/weekly/aa0924900a.htm

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 14, 2008 05:15 pm

Thyroid & Breast Cancer

I've found a couple of articles that link thyroid problems with breast cancer.  Does anyone know anything about this? 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 14, 2008 03:28 pm

What Questions do I need to ask?

Thank you to everyone.  Just thought I'd give an update. (if nothing else it makes me feel a little better to get this down than to have it just running through my head).  My PCP says the chest pain in caused by an inflamatory thing called condochondritis (? spelling).  She says taking ibuprophen will help with the pain. 

Now the countdown is on...4 days until I see the surgeon.  I'd be lying if I said I wasn't starting to freak out a little.  Everything under the sun has been running through my head.  I know odds are it will be B9, and I've already been told once 3 years ago that they thought I had thyroid cancer, the doctors were certain, when they did the surgey and sent the thyroid straight to pathology while I was still on the OR table to make sure the got it all...when to everyone's surprise...NO Cancer Cells!!!

I guess I'm a little worried that the same thing will happen again..you know the doctors think one thing but it will turn out to be the opposite.

I've got a list started of questions and topics I would like to discuss with the surgeon.  Even if this turns out to be B9 should I seek out a breast specialist to follow up with on a rutine basis?  I don't think I mentioned this before but I'll be turning 38 on Tuesday...Some B-Day present hugh? 

Do any of you gals & guys think that maybe what I have (if not BC) is a fibroadenoma?  I've been reading some about them here on the forum.  If it would be how often should I get rechecked?  Every year, six months? 

I've not told anyone yet what has been going on...my husband knows, and 2 good friends.  I've yet to tell my parents, brother, or 2 teenage sons.  I don't want to worry them until I know if there is something to worry about.  My husband says I should tell them something if not everything (which isn't much at this time), what do you guys think?

Thank you again for the support.  At a time with so much uncertainty it is comforting (what little you can get at a time like this) to know I'm not alone and that my thoughts (as runaway as they get sometimes) is normal. 

Posted in: Support & Community Connections + Young Women with Breast Cancer, Created: Sep 6, 2008 10:13 pm

I need feedback for speaking engagement

To me it sounds good.  I'm new at this game.  You mention that docs told you that you were too young...mine kept telling me, "oh, it's just changes from you cycle."  I always thought they knew what they were talking about, I guess not.  I see a surgeon on the 18th.   Maybe also mention about the risks even if you don't have any bc in your family history, I always thought I really didn't have to worry because no one in my family (anywhere) had bc. 

 Good luck I'm sure you'll do great. 

Posted in: Not Diagnosed but Concerned + Waiting for Test Results, Created: Sep 6, 2008 01:22 pm

Mammogram. Didn't hear what I wanted. Scared

I totally get where you're coming from.  I have to go for a biopsy on the 18th, from my mammogram and unltrasound both showed a tumor.  The spot they found on me was purely accident.  I was having chest pains and had seen a cardiologist (since there is a lot of heart problems in my family) but he said my heart was in great shape and not the cause for the chest pain (this after a stress test and heart cath).  I'm 38 and no one on either sides of my family has ever had breastcancer that anyone knows about. 

I don't know what to expect.  My PCP thinks the surgeon will take out the lump whole instead of a needle or core biopsy.  My PCP and I talked and she told me that a lot of times a needle or core biopsy will give a false result and that the only way to know 100% is to take the whole thing out and let pathology look at it as a whole instead of a few cells.

She also told me that most are B9 and to try not to worry.  I'll keep you in my prayers and pray we are both B9.  Good Luck. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 4, 2008 07:43 pm

lymph nodes & mammogram

I received my report to take to the surgeon on the 18th, and in reviewing the written report regarding the mammogram there is a sentence that I'm not sure how to take.  It simply states that "A single axillary tail lymph node is noted on the right."  Then the report goes on to describe the tumor that was found giving size and location. 

When my doctor spoke to me about my results of the mammogram and the ultrasound she did not mention anything about a lymph node.  It just bothers me that a lymph node was mentioned.  

Just wondering if anyone else has experienced this. 

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 1, 2008 08:35 pm

What Questions do I need to ask?

Thanks for the information.  My PCP said that it was more of an oval shape.  It had 3 different measurements but the largest one was 1.6 cm on mammo and 1.7 cm on ultrasound.  The tumor is located behind the nipple.  My appointment on Sept. 18th is to meet with the surgeon, I don't think he's doing anything that day, his office did send me a lot of paperwork to fill out and bring with me. 

Hope everything turns out good for you.

Posted in: Not Diagnosed but Concerned + Not Diagnosed but Worried, Created: Sep 1, 2008 06:58 pm

What Questions do I need to ask?

I just wanted to say thank you to everyone who has poured their heart out here. My journey is just beginning and I'm scared. My tumor was found by accident. I was having a problem with chest pain and the diagnosis they were giving me could only be reached by ruling out everything else first. I thought something might not be right when the tech who done my mammo told me not to be alarmed if I was called back in for an ultrasound. The next day I received that call. I went back in for the ultrasound and was contacted that evening that what they had found was not a cyst but indeed a solid tumor. They told me it would be OK to wait 6 months then have it reevaluated. They never told me that the specialist who read my ultrasound had recommended a biopsy, I found that out when I went back to my primary care physician. (which was 2 months later). So, now I have an appointment with a surgeon on Sept. 18th, who my pcp says will more than likely take the whole thing out then send off for biopsy because of the size and shape.

If I had not found this forum I think I may have drove myself crazy waiting. I wanted to say thank you to everyone who gave private details and thoughts for others to read.

Since I have no family history of breast cancer anywhere I'm not sure what all I need to be asking. I was going to take the wait 6 months and we'll check again as an answer, after reading here I'm glad I'm going on for biopsy.

© 2008 Breastcancer.org. All rights reserved.