› Forums › General Melanoma Community › Going to Mayo next Wed
- This topic has 4 replies, 2 voices, and was last updated 13 years, 9 months ago by ChristineL.
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- November 18, 2010 at 11:16 pm
I was diagnosed last Fri with Breslow depth 1.5 mm and Clarks level IV. I have my path report and it says on there that I am a stage Ib, t2a so far. Does anyone know exactly what that means. I have mitosis of 4/mm2, no ulceration, no regression, no tumor infiltrating lymphocytes. it does say radial and vertical margins negative, so that sounds good I think. Just hate waiting and want to get the WLE and SLNB next Fri most likely. Do folks think they will do the SLNB and how long of a surgery in my case? Thanks for any help/insight.
I was diagnosed last Fri with Breslow depth 1.5 mm and Clarks level IV. I have my path report and it says on there that I am a stage Ib, t2a so far. Does anyone know exactly what that means. I have mitosis of 4/mm2, no ulceration, no regression, no tumor infiltrating lymphocytes. it does say radial and vertical margins negative, so that sounds good I think. Just hate waiting and want to get the WLE and SLNB next Fri most likely. Do folks think they will do the SLNB and how long of a surgery in my case? Thanks for any help/insight.
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- November 19, 2010 at 12:37 am
Dave,
With a Breslow of 1.5 I would think you would be having a SNB. I would call and ask to make sure they are going to do it. I believe that standard practice for a SNB is now 1mm and larger without ulceration, and .75 and larger with ulceration. You will be sore but give yourself a few days and you'll be feeling better. Some people do take longer than others.
Good luck!
Linda
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- November 19, 2010 at 12:37 am
Dave,
With a Breslow of 1.5 I would think you would be having a SNB. I would call and ask to make sure they are going to do it. I believe that standard practice for a SNB is now 1mm and larger without ulceration, and .75 and larger with ulceration. You will be sore but give yourself a few days and you'll be feeling better. Some people do take longer than others.
Good luck!
Linda
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- November 19, 2010 at 12:55 am
Hi Dave,
Your initial staging is clinical staging, which is a starting point. They will be able to give you more information (the pathological staging) after the SNB (which will include the first one or several nodes), and hopefully you will remain Stage 1!! They usually do the SNB on depths >1mm (and sometimes less, depending on ulceration/mitoses), so they will probably do it in your case. Ulceration or mitoses >1/mm2 indicates that the tumor is a bit more "active". Not sure about how long the surgery will take, but mine took about an hour and a half. Before the SNB, they will inject a radioactive substance near the tumor site to see where it goes, i.e. which node(s) take it up first (these are the Sentinals). This may be more information than you care to know, but I have found information to be extremely helpful in understanding what's going on with me, the disease, etc, and actually puts my mind at ease. Not so much for others, though. I know the waiting is the hardest part, but try to get some sleep, and do the best you can to relax. Remember that you have many people on this board pulling for you as well. Please let us know when you get your results!!!
Take care,
ChristineL
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- November 19, 2010 at 12:55 am
Hi Dave,
Your initial staging is clinical staging, which is a starting point. They will be able to give you more information (the pathological staging) after the SNB (which will include the first one or several nodes), and hopefully you will remain Stage 1!! They usually do the SNB on depths >1mm (and sometimes less, depending on ulceration/mitoses), so they will probably do it in your case. Ulceration or mitoses >1/mm2 indicates that the tumor is a bit more "active". Not sure about how long the surgery will take, but mine took about an hour and a half. Before the SNB, they will inject a radioactive substance near the tumor site to see where it goes, i.e. which node(s) take it up first (these are the Sentinals). This may be more information than you care to know, but I have found information to be extremely helpful in understanding what's going on with me, the disease, etc, and actually puts my mind at ease. Not so much for others, though. I know the waiting is the hardest part, but try to get some sleep, and do the best you can to relax. Remember that you have many people on this board pulling for you as well. Please let us know when you get your results!!!
Take care,
ChristineL
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