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.

Zap_

Forum Replies Created

Viewing 0 reply threads
  • Replies
      Zap_
      Participant

      Hi Anonymous,

      I was diagnosed with Spitzoid melanoma Breslow 1.0mm, high mitotic rate, non-ulcerated, Clark Level IV. T1b. My doctors (surgeon, dermatologist) were not considering neither discussing SLNB, I did have the feeling that it should be done and after seeking advise from a melanoma expert, I decided to go for it. SLNB came back negative.

      https://www.melanoma.org/find-support/patient-community/mpip-melanoma-patients-information-page/newly-diagnosed-slnb

      As for for your specific case, I do not think the SLNB would have been necessary. For me it was a very personal decision and against the opinon of my doctors; for what I can see my case had worst prognosis than yours though, with risk factors involved (clark level, gender, age, mitotic rate).

      This was useful for me:

      https://www.skincancer.org/publications/the-melanoma-letter/2018-vol-36-no-1/ajcc-staging-system

      "guidelines state that for patients with T1b (<0.8 mm with ulceration or 0.8-1.0 mm with or without ulceration) melanomas, SLNB may be considered and discussed with the patient.22,26"

      So unless you had ulceration (for what you said I dont think so), SLNB would not be advised. Furthermore, after WLE has been done, SLNB may be more difficult (less accurate) to perform.

      Again, I am not as well informed as other users in the forum. But you seem to be on thin side of melanoma with a very good prognosis.

      That being said. I am lost with the Spitzoid myself. I asked about DecisionX factor and was told that due to the type (spitzoid) which as you said is quite rare, it may not be useful in my case, but I was not able to find a lot of info on it. My melanoma was in an area which is not very exposed to the sun and do not have any close cases in my family.

      Spitzoid or not, your prognosis at that Breslow level is very good and you should not worry too much (I know is easier said than done, believe me).

      Cheers!

       

      Zap_
      Participant

      Thanks Both,

      It is very useful to listen to your opinions, my biggest fear is that doctors here (living in Asia) are not  too used to deal with melanoma. They are good doctors, but do not see thin melanoma that often.

      This morning just noticed I have one more swollen node in my neck (again felt pain). Weird.

      Anybody knows if melanoma can spreed to non regional locations so fast – primary location on the back part of my right waist with SLN located in my right groin – ? I had a clear PET-CT scan on April and negative SLNB in June.

      Anyhow, is time to get it checked somehow and probably do more research on Stages III and IV (have been avoiding that and focusing on going on with my life)

      Again, appreciate a lot all your help. The informationon contained this forum has been crucial for me so far. 

       

       

      Zap_
      Participant

      OP here,

      Thanks as well for your opinion. honestly, I did get a little bit lost with all the info below (still rading and checking), but do appreciate your opinion about the SLNB.

       

      Zap_
      Participant

      OP here,

      Thanks a lot for the info Celeste. I do appreciate all the help. Have been reading your blog before and has been an extremely helpful source of resources, had not found the post you are sharing here though, so thanks for that.

      Did not make my decision yet, looking for a second opinion from a doctor back home. Is difficult being "lost in translation" when dealing with something like this.

       

Viewing 0 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 by MRF posting policies.