The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

SNLB

  • Post
    Aubreesmommy41
    Participant

      I'm second guessing some things tonight or overthinking maybe but for stage 1a .40 thick clarks level 2 no ulceration.. should I have had a SNLB? All I had was a WLE. Just wondering. 

    Viewing 2 reply threads
    • Replies
        jennunicorn
        Participant

          No, the standard of care is to do a SLNB for 1.00mm or larger and is considered sometimes for 0.75-1.00mm if other things such as ulceration are present. You can't have a SLNB after getting the WLE anyway, there is no way to go back and do that, so no worries, you took the right steps.

          jennunicorn
          Participant

            No, the standard of care is to do a SLNB for 1.00mm or larger and is considered sometimes for 0.75-1.00mm if other things such as ulceration are present. You can't have a SLNB after getting the WLE anyway, there is no way to go back and do that, so no worries, you took the right steps.

            jennunicorn
            Participant

              No, the standard of care is to do a SLNB for 1.00mm or larger and is considered sometimes for 0.75-1.00mm if other things such as ulceration are present. You can't have a SLNB after getting the WLE anyway, there is no way to go back and do that, so no worries, you took the right steps.

          Viewing 2 reply threads
          • You must be logged in to reply to this topic.
          About the MRF Patient Forum

          The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

          The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

          Popular Topics