Mets to ribs or sternum

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Hi all! For 4 months my gp and gastroenterologist have been testing me for issues with gallbladder or colon. I have had an egd, ct of abdomen, hida scan, and colonoscopy. Nothing showed any abnormal issues. I have nausea or vomiting daily. Also I have severe diarrhea within minutes after eating, regardless of food type. 

My pain started under right breast and now is totally across upper abdomen and radiating to center of breasts. Also to center of my back. I see my MO 8/13. Anyone with these symptoms? I really thought when I met with a surgeon, I was going to have my gallbladder removed. So confused. My pain is worse when lying down. Thanks so much!

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  • leggo
    leggo Member Posts: 3,293
    edited August 2014

    Hi steelergirl. Hope you get to the bottom of it on the 13th. As for mets to ribs and sternum and a reference, I have both. The rib mets feel like broken ribs (if you've ever broken one, that's what it feel like). The sternum mets are quite painful. When I was first diagnosed, it hurt to clear my throat, cough, even breathe. When I sneezed, I almost passed out. Also, back pain, which sometimes hurt as much in the back as in the front, even though I didn't have spine mets at the time. I also had a quite  palpable lump there. Those were my physical symptoms, along with generally feeling unwell. No nausea, no vomiting with those mets. I assume you're liver has already been looked at? Good luck to you.

  • steelergirl65
    steelergirl65 Member Posts: 8
    edited August 2014

    Thanks leggo! It even hurts to wear a bra! My pain is persistent 24/7. Much worse when I lie down. May I ask what type of testing found yours? I've read conflicting advise on the web about ct, bone scan, mri or pet scans. Thanks again for your support!

  • leggo
    leggo Member Posts: 3,293
    edited August 2014

    This all happened back in '06. I had a persistent pain in my chest and in my ribs and it hurt when I rolled around in bed. Doctor sent me for an x-ray in April,  which showed nothing out of the ordinary.  By July it was getting worse and it started to hurt when I twisted. Doctor figured it was costochondritis and started treating me for that with anti-inflammatories and cortisone shots. That didn't really help. I told him that I thought my cancer was back and he told me that it would be a strange place for cancer to spread, especially since I had been cancer-free since '95 (he obviously was soooo wrong). He was sure it was costochondritis and it would take a while for treatment to work. Whatever, I was naive and took him at his word. By November, it was hurting to cough and sneeze and I felt like crap.  In December, at work, I lifted a box of paper and I heard a snap and the pain brought me to my knees. Luckily, I was working in a hospital, so I got wheeled down to Emergency where another x-ray was ordered, followed by a CT and a bone scan. Doctor said he ordered all three because he wasn't sure what they were looking for. Got the bad news that night. Those were the only two scans I got, along with the x-ray but after those, I had already been told it was probably cancer by the results of those scans and they were going to schedule a biopsy to confirm. Never had a PET, to this day. I did have one MRI, later on when I had further spread, but that was when I needed rads to the spine and they needed the extra view.

    I've seen several women on here blown off with the costochondritis story, so I try to tell everyone I can that it should be looked into further if they have a history of bc.

    I sincerely hope you don't have to go through any drama to find out what's wrong and that when you do, it's something less serious. Just don't let anyone tell you it's costochondritis if it isn't getting better. I learned the hard way, with months of needless suffering. Hope to hear good news when you get to the bottom of it.

  • steelrose
    steelrose Member Posts: 3,798
    edited August 2014

    leggo,

    Your story is very important!! I'm dealing with a similar situation right now, although I was diagnosed stage iv in 2010. Six months ago I developed pain in the ribs. Since then I've had... count 'em... 3 CT scans, 1 MRI, 1 bone scan, and 1 ultrasound... all coming out clear except for a bit of "uptake" in my right ribcage, where the pain is. The oncologist thinks it's nerve damage from my spinal surgery and rads in 2010. And she also mentioned the possibility of costochrondritis! I had an epidural to my back about a week ago, but I think I'm in more pain than before! My point is for steelergirl to push for answers if you're in doubt! And then keep pushing! I sincerely hope it's nothing serious. But you can't tackle it if you don't know what it is. Ignorance is NOT bliss!

    Wishing you the best!

    Rose.

  • steelergirl65
    steelergirl65 Member Posts: 8
    edited August 2014

    Thanks y'all for your supportive input! Last gp visit I was told it could be costochondritis....wow, go figure! That's why I'm following up with my MO. Whatever if is, something's not right. When I found my lump, my Dr was out of town. His on call dr told me to wait about six months and have it rechecked. Needless to say, I didn't listen and was diagnosed 2 days later. My MO told me if I had waited that long, my prognosis would've been poor. 

    Thanks again so much!

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