MOHs BCC removal from nose and cheek flap reconstruction

FormerMember
FormerMember
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I've had a first consultation with my plastic surgeon who confirmed a nodular BCC on my nose (although I still haven't had a biopsy).  After reading many posts on this website I was expecting Mohs to be offered as the ulcer is 1cm and approx 3mm thickness but the surgeon has said excision with a skin graft from infront of my ear.  He said that as it was "mushrooming" over itself, it shouldn't have spread outside it's boundaries and so Mohs wouldn't be needed. He also said there will be a mismatch of colour after the op and I will need reconstruction of my nostril.

I guess I am looking for reassurance that excision can be just as successful as Mohs and to trust the surgeon that it hasn't spread. I did tell him I was having infrequent dull ache on the cartilage further up my nose but he said that once you know you have skin cancer you can attribute any ache and pain to it incorrectly.
Separate to this my GP put me on antibiotics as I am having pain in my side by kidney and peeing more often and Ibuprofen for swollen  glands and tonsil. I of course am thinking of cancer spreading to lymph nodes...but have read that BCC rarely spreads.
I would be greatful for any advice from someone who has had excision of a BCC of around 1cm on nose.
  • Hi and a very warm welcome to the online community

    I'm sorry to hear that you need to have surgery to remove a BCC from your nose. I know how stressful this can be and it's natural to wonder if you've been offered the best treatment.

    Most BCCs are removed by simple surgery, like you're being offered, and Mohs is generally only offered for complex BCCs. Your surgeon will remove an area of healthy tissue around the BCC as well as the BCC and this will be sent to the pathology lab to check that all of the BCC has been removed. On the rare occasion that it hasn't then a second procedure may be needed. If you click on this link it'll take you to BAD's (British Association of Dermatologist) information on BCCs and how they're treated.

    There are lots of people in the group who have had the type of surgery that you're having and you could use the search facility at the top of the page to narrow down your search to look for older posts which mention it.

    It's very common to fear the worst when you've been diagnosed with cancer and to think that every little ache and pain means that it's spread. We've all been there! Your body has let you down and you need to learn to trust it again. Hopefully, the antibiotics will do the trick but if your symptoms persist, or get worse, then I'm sure your GP will have told you to go back.

    Do you have a date yet for your surgery?

    x

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  • FormerMember
    FormerMember in reply to latchbrook

    Thanks Latchbrook, yes Aug 11 is my op date.  There were so many questions I thought of asking once the consultation was over so I have sent an email to the dept.  I'm just about the have a look on this site for post op care to see if I need to stock up on anything

  • Well from my experience of having excisions you will probably be told by your team to have a supply of paracetamol and ibuprofen ready. Depending on your pain threshold you might find that you don't need to take anything. When I've had simple excisions I haven't needed anything but when I had a wide local excision and sentinel lymph node biopsy after being diagnosed with melanoma I found I needed to take both types of painkillers together for a couple of days.

    Let us know how you get on and, if you think of any more questions, just fire away.

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  • FormerMember
    FormerMember

    Hi Catladyx

    am sorry to hear you have a bcc, I’ve not been able to get on here to reply to people, I had bcc on tip of nose plus one a bit further up, I had MOHs then a paramedium  forehead flap, then reconstruction separation, that was last October, It was a long process but worthwhile as unless I tell someone you can’t even tell I’ve had surgery, I don’t know about just having an excision, so I can’t help there,  I would ask why MOHs isn’t suitable for you, it’s difficult without knowing full history, you have to put your trust in the surgeon, they are the experts and every case is different, 

    good luck 

    Frankie1 

  • FormerMember
    FormerMember

    I had MOHs surgery yesterday which was cleared after 2 stages. I then had a cheek flap reconstruction.  So far, other than a bit of bleeding and not being able to open my.mouth too far due to the stitches, I'm feeling pretty good.  

    The staff at St Helens were incredible.  I can honestly say I felt absolutely no pain at all.  They gave me an injection like you get at the dentist which totally numbed my nose ready for the main injection.

    The dressing is on for a month *sigh* but I can't grumble as the overall experience was a very positive one.

  • I'm glad to hear how well things went . Hopefully others who come here worried about upcoming surgery will read about your experience and feel less anxious. Slight smile

    Keep us up to date with how thing's progress.

    x

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