Question about Pathology report of SLN Stage 3A

Forums General Melanoma Community Question about Pathology report of SLN Stage 3A

  • Post
    CCCL
    Participant

      Hi ,

       

      I recently had my Sentinel Lymph Node surgery, and it they found 1 out of 5 nodes positive with 1 mm dimension of tumor burden in the positive node. I am going to be doing the CLND in a week or so. I have read a lot of the information on this forum and the internet as a whole and its been great to get a better understanding of everything. The question I wanted to see if anyone was familiar with was the pathologist listed a % of how much cancer I guess was in the Lymph Node. I haven't read about that anywhere, so I wanted to understand the significance of it. 

       

      Here is exactly what the pathologist said on the report:

       

      Largest Metastatic focus measures 1 mm in greatest dimension, involves less then 10% of lymph node area,  subcapsular and intraparenchymal location, no extracapsular extention indentified.

       

      So I have a good idea of all of the other info outside of the "10%" of lymph node involvement, I haven't seen anything like that anywhere on the internet so was hoping someone here might be familiar it. I am just wondering if it has any significance in terms or good or bad factors. 

       

      Thank you for your help ahead of time. 

      CC

    Viewing 2 reply threads
    • Replies
        Thandster
        Participant

          that is just saying that roughly 10% of the area of the node has the melanoma in it. Picture the node as a tea cup and only 10% of that cup is full. 2 of mine were 50%. some people will have 100% with extra capsular extension meaning the tea cup  is totally full and overflowing out the top.  Overall, the lower percentage the better chance that it all stayed in the cup (node) and it didn't spread further although this is melanoma and there are no sure things. If the cup is overflowing it is more likely to have spilled out of the cup and spread.

            CCCL
            Participant

              Thanks for the information, It makes sense the way you described it, its just so much info that they throw at you sometimes you can't think straight. 

               

               

              CCCL
              Participant

                Thanks for the information, It makes sense the way you described it, its just so much info that they throw at you sometimes you can't think straight. 

                 

                 

                CCCL
                Participant

                  Thanks for the information, It makes sense the way you described it, its just so much info that they throw at you sometimes you can't think straight. 

                   

                   

                Thandster
                Participant

                  that is just saying that roughly 10% of the area of the node has the melanoma in it. Picture the node as a tea cup and only 10% of that cup is full. 2 of mine were 50%. some people will have 100% with extra capsular extension meaning the tea cup  is totally full and overflowing out the top.  Overall, the lower percentage the better chance that it all stayed in the cup (node) and it didn't spread further although this is melanoma and there are no sure things. If the cup is overflowing it is more likely to have spilled out of the cup and spread.

                  Thandster
                  Participant

                    that is just saying that roughly 10% of the area of the node has the melanoma in it. Picture the node as a tea cup and only 10% of that cup is full. 2 of mine were 50%. some people will have 100% with extra capsular extension meaning the tea cup  is totally full and overflowing out the top.  Overall, the lower percentage the better chance that it all stayed in the cup (node) and it didn't spread further although this is melanoma and there are no sure things. If the cup is overflowing it is more likely to have spilled out of the cup and spread.

                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