Mucinous adenocarcinoma ( appendix cancer )

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Hi , I’m not sure if I belong in this group but they did put a leaflet in my pre -op pack , also referred by Sarah. 

I had an  appendectomy mid June ( appendix had burst and create an abscess) .
i was told on 3/7 it was cancerous and i would be referred to a specialist hospital for right helicolorectomy and HIPEC ( hot chemo wash in the abdomen ) I’ve been told it is grade 3 .
my local hospital thought the operation would be in August  and it had been caught early. 
To date I’ve had no treatment . 
After eventually getting a date for the op of the 28/9 , it was cancelled on Thursday . The latest scans have revealed it is currently inoperable and I have to have 3 months chemo to try to shrink some of the cancer. 
I have an appointment back at the local hospital on Friday (2/10) .to discuss chemotherapy.

there have  been lots of tears at each delay and feelings of frustration and being let down by the system which is ultimately going to cost my life .  I’m guessing lots of you have felt like this ?

Does anyone have experience of this type of cancer ?


Im seeing my original consultant on Friday , any ideas how long I will have to wait for the chemo to start .
ive read this type of cancer doesn’t always respond to chemo , so the ideal is to remove it by surgery 

does anyone have any experience of going private for this  - currently considering all options , I don’t think I have time to wait . 

  • Hi Jacq100

    if you are seeing your Consultant on Friday, the process is that they refer you to the Oncolgy Team for chemo. As soon as you have seen this team it doesn’t take long at all for the chemo to start, probably about 2 weeks. I was operated on at The Christie in Manchester in Feb 2025. It is not straightforward and I have had another 2 operations for small bowel obstruction done at my local hospital. There are only 2 hospitals specialised to deal with PMP and I would stick with them. It is frustrating the waiting but a few more weeks won’t make any difference. I was told the appendix tumour could have been there for 10 years. 

  • Thank you , I’m trying to be patient ! It’s good to hear from someone who has been through it. 

  • Hi

    Do you know why they said you were inoperable? Was that a Consultant at The Christie in Manchester and the Basingstoke Hospital in Hampshire? I am a Christie patient and Christie Consultant arranged for a 2nd opinion at Basingstoke Hospital.  The two teams work closely together.

    Suggest you join the charity Pseudomyxoma Survivor private FB group as there are lots of patients who are members with lots of experience.

  • I think it was the increase in number of cancerous nodes  and their location in the pelvis. Yes I was to be operated on in Manchester. The cancellation was a phone call and I was in shock . Iwill join the group. Thank you 

  • Yes please join the Pseudomyxoma Survivor Group.  My Consultant at The Christie arranged my 2nd opinion at Basingstoke.  

    I am on FOLFIRI chemo and according g to my last scan, disease is stable .....I am inoperable due to involvement of small bowel.