Liver mets symptoms?

  • 11 replies
  • 11 subscribers
  • 256 views

Feeling tight and pain around my right rib, a bit concerned. 

  • Hi 

    I can’t comment on this particular symptom as I haven’t experienced it but I have been to my GP on several occasions regarding new pains etc. I was diagnosed in June 2022. It was very reassuring as they educated me re pains from likely metastasis versus other bodily pains. I very rarely attend my GP in general but they had complete understanding and compassion. Certainly didn’t make me feel I was wasting their time. I would certainly recommend visiting your GP for peace of mind. Good luck 

  • Not symptoms I can comment on, but I presume you are on regular scans, and that you have been given nurse contact details etc.?

    Perhaps if you don't want to trouble a GP, speak to one of those nurses?

  • I am experiencing similar symptoms to you and wanted to ask if you got this checked out? I have a liver scan in the next month but I am feeling very nervous  

    I had proton beam in February 2025.

  • Hi there, thanks for your message. I feel for you. xx

    As an update - it started just before Christmas 2025, I got little pinpricks in the right rib area and they stayed in the same place, and my bra line got tighter. If I leant against the table it was uncomfortable. This hasn't gone away, has stayed in the same place, and has got much worse - it is now noticeable most of the day every single day, and I also feel it in the left hand rib too, and also as shooting pains up to my neck. I haven't gone yellow yet! But the pain is there. I have had a lot of family things this year, two weddings, two driving tests, the kids moving house, a pregnancy announcement etc, so it just hasn't been the right time to share it. Pensive

    It has now been therefore about 7 months since I first noticed the pain, and I feel it now pretty much all day, (although there are some days when it is a bit less noticeable) when I hang up washing, when I lean forward, when I lean back too, onto a hard chair, when I twist around sometimes, etc. 

    The worst thing is, I went to Moorfields 2 weeks ago for my 2 year check, and as per usual I saw a 'substitute' doctor, and after the usual tests (I had brachytherapy 2 yrs ago) she gave me about 5 minutes. My tumour is the same size pretty much that it always was before the treatment, but I mentioned it to her, and she completely brushed me off and said "It won't be your liver, it's most likely your gallbladder" so I left feeling like an idiot! (My tumour was quite shallow, but was 9mm x 9mm at the base.) 

    I went home and researched liver pain as opposed to gallbladder, and it definitely isn't my gallbladder, as that apparently takes years to get irritable and inflamed and it usually presents as sudden and intense pain, more in the centre of your abdomen, (my pain is quite far round to the right, and also far left, and also right up under my ribs) and especially always after eating high-fat meals. People apparently often go to A & E because they think it is a heart attack. Mine is nothing like that. It is constant, (and growing weekly) and eating doesn't change it, and it is sometimes sharp, and sometimes dull, but always in the same places. I feel it when I wake up and when I go to sleep, I feel it after eating and/or before, and it is not so intense that I am in terrible pain suddenly, it is not a tummy ache! 

    The other thing is that I looked up "Can you feel an enlarged liver (like from mets) from the outside?" (Because in Jan and Feb and March, I couldn't, but now if I press a little under my right rib, when lying down, and I breathe in, I now clearly feel a 'rolling' sensation of something quite big moving and rolling under my hands.) I read that this should not happen, and that the liver is usually well hidden under the ribs, even on breathing in. This is not what an irritable gallbladder presents as I don't think, as the gallbladder is hidden inside/under the liver and is pretty small. And I have only had this in the last month or so. 

    I hope I haven't worried you, but if you are like me, I feel that information helps us all, and as there are so few of us, we often get brushed off with not much info at all! 

    Have you had liver scans up until now regularly since the proton beam therapy? 

    They didn't biopsy mine and I don't get scans, as they said it was on the borderline for such. (That was also Moorfield's decision!) But I read somewhere that without scans and a biopsy, they don't know whether mine is high risk for metastasis or not!

    So I don't think the doctors should really be ignoring my symptoms, especially when the two to two and a half yr mark after treatment is supposed to be the prime 'median' time for mets to show itself??!

    Please let me know how things go for you and what happens, and are your symptoms the same and how long have you had them? (If you didn't mind.) 

    Take care, 

    xx

  • Thanks for your reply! 

    I have had regular liver scans every 6 months since December 2024. All have been clear except one showed a hemangioma so I had an MRI after that but was told it was fine and not spread. Have you had a liver scan since your pain started in your ribs? 

    My last eye scan at the hospital showed that my eye tumour had flattened since the radiotherapy, which was really positive  

    I have only had slight discomfort under my ribs, it feels like a full feeling. I am quite conscious that it could all be in my head as I know I have a liver scan coming up. I followed up today with the hospital on when my appointment is, so I will keep you posted  

  • Sorry if I replied to this sooner, I'm not sure if I did, but on re-reading, I should answer - no, I am not having any scans, as my tumour was shallowish and 9x9 mm at the base and Moorfields told me it was on the border for any follow ups like that on my liver. So they didn't biopsy and they didn't ever do any scans. 

    Hope you are well? 

    Take care. x

  • Actually had my 4th MRI yesterday. In that sweaty "wait" for results phase. Otherwise good.

  • No worries! x

    I haven't had any scans, no. the first I mentioned this was at the hospital appt 2 weeks ago, where she told me I was just being silly and that it could only be a gallbladder issue. (Which I've never had, and is not in my family history anywhere and I don't eat high fat meals!) I felt like a complaining moron so I just left it at that and walked away, actually feeling pretty 'unheard' and brushed off. I suppose I should try my GP next at some point, but they don't know anything about ocular melanoma either and are very slow to help! 

    Well done for chasing up your appt. It does sound a bit similar to my pains. I will come back here if I get any news too, I hope it helps you too. 

    Take care! xx

  • Aaw, I hope all is well, please come back here to let us know what happens! And I'm sorry you are in that horrible waiting phase. It sucks doesn't it? xx

  • Given your story on this, raise this with Moorfields PALS set up. Can't promise a change but at least it raises flags with "higher" in the set up.