Anyone had Metastatic Squamous Cell Carcinoma?
Has anyone else dealt with this type that was evident in lymph nodes?
Interested in more discussions like this? Go to the Head & Neck Cancer Support Group.
Has anyone else dealt with this type that was evident in lymph nodes?
Interested in more discussions like this? Go to the Head & Neck Cancer Support Group.
You need to go see an ENT ASAP to find out what this doctor is talking about. They seem very irresponsible to me with giving you the wrong diagnosis. Do this immediately
Hi Myrtle, I can imagine that you’re scared. This is something you need to have investigated immediately and it sounds like your dermatologist is referring you back to your PCP for testing or further to make a referral to an oncologist. It is possible that the cancer has moved to the lymph nodes. To rule out or confirm this, the likely test will be a biopsy. You can read more here:
- Squamous Cell Skin Cancer of the Head and Neck https://www.hopkinsmedicine.org/health/conditions-and-diseases/squamous-cell-skin-cancer
Have you made an appointment with your doctor? We’re here for any questions you have along the way. You’re not alone.
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1 ReactionI seen my PCP yesterday. He is sending me for an ultrasound first. He said if that didn’t give us any answers he would send me to get another test (forgot the name) where they go down my throat with a light.
I have metastatic SCC, initially diagnosed in 2012 but with lung metastasis twice, a small tumor on a muscle, and finally metastasis to a kidney and lymph nodes. It can show up anywhere. You need to see an oncologist as soon as possible. It is beyond the scope of a dermatologist or primary care doctor. There are new immunotherapies approved for use for this disease and better prognosis has resulted. I am on one called Libtayo through my oncologist at Mayo Clinic, Rochester MN. and my tumors are gone at this point. There they use whole body CT scans or PET scans to check for metastases regularly. I also take Vitamin D, Curcumin, Beta Glucan supplements and a daily probiotic for immune support. Do your research and good luck to you.
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1 ReactionThank you for the information. I’m still waiting on the ultrasound approval from my insurance. I’m thankful I found this page.
@missy22, how are you doing? Four months to get a cancerous tumor removed seems like a very long time to wait. Do you know if it is slow growing? Did they biopsy the other spots on your leg or chest?
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1 ReactionIt is so encouraging to hear of your results. I'm curious as to what insurance you had, as I have not been able to access these treatments despite similar diagnosis.
Welcome @youngpepper. You also have Metastatic Squamous Cell Carcinoma? In the head and neck region? What treatments options have been offered to you?
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1 ReactionRadiation and chemotherapy. Mine started out as HPV 16 positive tumor lower tongue and right tonsil area. Could not get reduced radiation so I have been trying to get into a clinical trial or better yet you immuno therapy. However now I have a mass that has turned to t4 n3, this was after almost a year and a half of slow progression. I was trying to get into the Keytruda trial that was being offered , but my insurance is not accepted for the testing so I cannot even try to get in. I might just as well have taken the excessive radiation and chemo and dealt with the toxicity if this were to be the case. Obviously, I didn't understand how the system worked. Or should I say how it doesn't. I don't mean to sound bitter, but I am angry that I was not given either opportunity or any choices. It was, after all, my life.
I hope that you find a trial that will accept you. Keytruda, Opdivo and other PD-1 PD-L1 immuno-oncology are effective agents for gastro-esophageal cancers. I was diagnosed with metastatic ESCC on 1/2019 and was treated with aggressive chemo radiation. I had a good initial response as evidenced by scans but recurrence/mets after 9 months. Started FOLFOX + Keytruda. Tolerated 3 doses of Keytruda before I had to discontinue due to exacerbation of of my MS. That said, I had a remarkable response to therapy with marked shrinkage/attenuation of all lesions and no new mets. Currently on FOLFIRI. So far so good.
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