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.

Jenncat0402

Forum Replies Created

Viewing 9 reply threads
  • Replies
      Jenncat0402
      Participant

        Mine was .9 and I have the SLNB and have not regretted it once. It just gives some reassurance if there is nothing there but there have been cases even with a low bresliw there could be microscopic cells in the lymphnodes.

        Jenncat0402
        Participant

          I would highly recommend having the SLNB. Mine was .9mm and almost the exact same path report. I was 27 when I was diagnosed in December of 2014. I did not want the risk of the unknown if there were micro mets and they would show up years later, or even months from then.  There is always the chnace that it will show up years later without the SLNB but it gave me a peice of mind now. I also had the decision dx done as well. When it is a stage 1 or 2 this is a better predictor of later metastis from reportings. Different Drs recommend  SLNB at different depths my Dr typically at 1mm but with mine being .9mm they recommended it so if she is worrying at all I would say do it. It is really the preference of the Dr and patient.

          Jenncat0402
          Participant

            I would highly recommend having the SLNB. Mine was .9mm and almost the exact same path report. I was 27 when I was diagnosed in December of 2014. I did not want the risk of the unknown if there were micro mets and they would show up years later, or even months from then.  There is always the chnace that it will show up years later without the SLNB but it gave me a peice of mind now. I also had the decision dx done as well. When it is a stage 1 or 2 this is a better predictor of later metastis from reportings. Different Drs recommend  SLNB at different depths my Dr typically at 1mm but with mine being .9mm they recommended it so if she is worrying at all I would say do it. It is really the preference of the Dr and patient.

            Jenncat0402
            Participant

              I would highly recommend having the SLNB. Mine was .9mm and almost the exact same path report. I was 27 when I was diagnosed in December of 2014. I did not want the risk of the unknown if there were micro mets and they would show up years later, or even months from then.  There is always the chnace that it will show up years later without the SLNB but it gave me a peice of mind now. I also had the decision dx done as well. When it is a stage 1 or 2 this is a better predictor of later metastis from reportings. Different Drs recommend  SLNB at different depths my Dr typically at 1mm but with mine being .9mm they recommended it so if she is worrying at all I would say do it. It is really the preference of the Dr and patient.

              Jenncat0402
              Participant

                My melanoma was also on my anterior deltoid. My derm did not want to do it she recommended a plastice surgeon. I am really glad i went with the plastic surgeon, even though the scar is 6" it looks amazing even after only 7 months. If you have to have a SLNB like I did I had a general surgeon do that at the same time the plastic surgeon did my WLE.

                Jenncat0402
                Participant

                  My melanoma was also on my anterior deltoid. My derm did not want to do it she recommended a plastice surgeon. I am really glad i went with the plastic surgeon, even though the scar is 6" it looks amazing even after only 7 months. If you have to have a SLNB like I did I had a general surgeon do that at the same time the plastic surgeon did my WLE.

                  Jenncat0402
                  Participant

                    My melanoma was also on my anterior deltoid. My derm did not want to do it she recommended a plastice surgeon. I am really glad i went with the plastic surgeon, even though the scar is 6" it looks amazing even after only 7 months. If you have to have a SLNB like I did I had a general surgeon do that at the same time the plastic surgeon did my WLE.

                    Jenncat0402
                    Participant

                      I had this done as well. Mine came back class 1 with negative SLNB so they are saying the probability of mine returning is less than a class 2 with Negative SLNB. I am only 7 1/2 minths out from dx and there aren't too many studies on the results so I dont know about the long term. But i am hoping they are correct with the results πŸ™‚ my derm in my hometown did not even know what the test was but my derm in the city is the ine who sent it off so it is relatively new.

                      Jenncat0402
                      Participant

                        I had this done as well. Mine came back class 1 with negative SLNB so they are saying the probability of mine returning is less than a class 2 with Negative SLNB. I am only 7 1/2 minths out from dx and there aren't too many studies on the results so I dont know about the long term. But i am hoping they are correct with the results πŸ™‚ my derm in my hometown did not even know what the test was but my derm in the city is the ine who sent it off so it is relatively new.

                        Jenncat0402
                        Participant

                          I had this done as well. Mine came back class 1 with negative SLNB so they are saying the probability of mine returning is less than a class 2 with Negative SLNB. I am only 7 1/2 minths out from dx and there aren't too many studies on the results so I dont know about the long term. But i am hoping they are correct with the results πŸ™‚ my derm in my hometown did not even know what the test was but my derm in the city is the ine who sent it off so it is relatively new.

                          Jenncat0402
                          Participant

                            Thank you so much for replying. I keep hearing it is very rare as well I have had contradicting answers, some say it id better some worst and somecsay there is no difference between any other melanoma πŸ™ i just wish there were more information out there on it. 

                            Jenncat0402
                            Participant

                              Thank you so much for replying. I keep hearing it is very rare as well I have had contradicting answers, some say it id better some worst and somecsay there is no difference between any other melanoma πŸ™ i just wish there were more information out there on it. 

                              Jenncat0402
                              Participant

                                Thank you so much for replying. I keep hearing it is very rare as well I have had contradicting answers, some say it id better some worst and somecsay there is no difference between any other melanoma πŸ™ i just wish there were more information out there on it. 

                            Viewing 9 reply threads
                            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 byΒ MRF posting policies.

                            Popular Topics