lung cancer

I would like to discuss my mum (56) who has been told by the doctors that they are highly suspicious she has lung cancer (either in the lung from the lung or from somewhere else) after having pnuemonia. A CT scan has shown multiple pleural based soft tissue masses throughout both lungs the largest measured 34mm x 19mm the appearence consistent with multiple pleural and parenchymal metastatus. She had a bronchosphopy today and they took cells and scrapings and also removed a polyp to all be analysed. They will give mum the results on Wednesday next week. They have said that there may be no abnormalities found it may all be inflammatory, that they couldn't look at the masses as they are in the lining of the lung and that once they get the results they will then do another xray or CT and maybe a CT guided biopsy of one of the spots on the lung. The doctors have left us very confused today. We have gone from thinking the worse to thinking maybe this will end up being not even cancer. I should add my mum stopped smoking 3 years ago after smoking since being young and also suffers from rheumatoid arthritis. All of her other organs on the CT between chest and pelvic appeared normal. The original CT scan said there is evidence of superior mediastinal , paratracheal lympahadenopathy. Please can you help by giving me your views on what you think will be the outcome of my mums results. Its sending me mad not understanding or knowing.

  • Hi Chazchloe = poor you - and mum having to wait while all these tests go on!! There is something there in the lung area - but they can't deal with it, until its well understood. So far - there seems to be a couple of alternative diagnoses - so futher tests are needed to whittle it down. Well, thats all quite a journey. I am so glad mum is no longer smoking - that will give her a good chance. Tell her to stay positive and keep bouyant.

    Some times these things take time - but that doesn't mean they are dragging theri feet = it simply means its complex. Mean times - just offer to mum that this hanging about is making it hard for you. Some times life is very uncertain and we don't know what to do! Its at those times we can only reach into ourselves and find our inner strength to be there for others.

    The way will be clearer soon

    xx

  • Thank you for your reply. Is it normal do you know for these things to take weeks of different tests until you get a correct diagnoses. people keep saying that surly if its cancer they would know by now. I have been reading so much about all the different things that can cause inflammatory changes in the lungs, I understand how many different things that could be, but on the CT report the mention of the masses and sizes etc when you read about what all of those words mean it doesn't mention inflammation. I don't really understand why at the MDT meeting they decided to just do the bronchosphopy and not a CT guided biopsy if she may end up having to have one anyway later. I know I just have to wait and that the cells will tell them a lot and we will get answers. The doctors are so calm, I just think this is my mum and I need to know now! I don't understand why the approach wasn't different at the beginning they could have said its inflammation and a small chance of cancer but that's not how they delivered the news to us. Now they seem to have changed there approach, however it depends on which doctor talks to you. Obviously we will be so pleased if this ends up to be nothing serious, but it doesn't change that we have gone through hell to get to that conclusion. Please don't think badly of me as I realise that other people chatting in here are in much worse situations than us. This is all new and I just dont understand the whole process.
  • Hi chazchloe = thank you for answering. Yea the wait is endless = but on the positives - you and her have a close relationship and she is doing okay. Let the doctors fiddle on at their own speed. Something like this happened to my aunty = they saw a cancerous lump on her lung - she was in the next day having it out. That this hasn't happened to mum would suggest that its going to be okay. So, this is a time of reflection and waiting = enjoying what together you have..

    I don't think badly of anyone = gosh - I asked my work colleagues only the other day how I was on hearing the tests were needed = I was in blind panic!! Feelings are facts - they are the basis of our living and some times they are stronger than our thoughts. We can't always be logical and the times when we scream at life "ENOUGH"! - is a good time. They say that our bodies are always in the real world - its our thoughts that go up annd down and if they can be rooted in our bodies - then we would be fine.

    XX let us know what happens

    Steven X

  • Thank you I will let you know when I know more. At the beginning after the pneumonia and after the CT scan they said if this cancer then they wouldn't be able to remove them as they are in both lungs they would offer RT or chemotherapy. now they are suggesting steroids might help, so let hope as you say that this time for answers equal better news. Thanks Ill keep you updated.
  • Just thought that I would give an update as it may also help others if in a similar situation. My mum had her bronschoscopy last week. The consultant took cells and scrapings of inside the lung and removed a polyp for analysis. He said afterwards he was happy with what he saw inside. We went for the results today, the cells that were taken are not malignant, the polyp results are not back yet. Mum had a repeat xray and the consultant compared all xrays and CT result to today's xray. A lot of the shadowing has gone and the left lung now looks clear. Two areas of shadowing are still in the bottom and mid right lung which he has asked for a repeat CT scan on with in 2 weeks and if still visible then has asked for a biopsy of them. These are in lining so were not visable during the bronchoscopy. They found pnuemonia and another bug from the samples. I cant remember the name of the other bug but apparently this is not treatable and can be active and not active? The doctor was very positive today and he feels that the other areas may not be cancerous either. he wants to see mum in 4 weeks for any results and to see if it may have all improved even more. Everything seems so much brighter today, her lungs are now improving so the outlook is not as scary. Now just hoping all of this has just been a horrible dream!