8 mm lung nodule possible malignancy: What should I do?
I had a CT scan and they found a nodule which has grown to 8 mm from 6 mm 12 months ago. The report says "slowly growing malignancy cannot be excluded". My doctor (GP) recommends another CT in 3 months but I am concerned that this approach is not aggressive enough. It has clearly changed from 6 mm to 8 mm.
What do I do?
Should I be seeing an oncologist now?
Should something more aggressive me done?
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I've read that any nodules 8mm should be looked at in an aggressive manner. But, for comparison, yours is slow growing compared to my husband's 6mm grew to 8mm in 3 months. Plus he has 7 nodules 6mm or larger and all have grown just in 90 days. Hope this helps.
I did actually use Google and it brings up a chart showing a peanut, a pea, etc. Lists the sizes in mm and cm. It gives you a pretty good idea. A radiologist reads your CT. If you are seeing a Pulmonologist they are looking at the results as well. The Dr tht read mine was quite accurate. Of course, make sure you ask questions if you’re not sure. They measure it again when they get it out.
Do you have a mm scale to see the size you are talking about? How accurate is the person reading your CT scan?
I had my CT scan here locally on January 5th, 2023. It took them 2 weeks to send the results to my doctor. I had my PET scan at Mayo around the end of February and had my segmentectomy March 24th, 2023. Whirlwind of appointments in between!
Hello skm101-
After my Dr saw my CT scan he called me and said he wanted me to have a PET scan. He sent the order to our local hospital and when they called me to set up the appointment I called him and told him to send it to Mayo instead. I believe(not 100% sure) that you can go on the Mayoclinic.org website and request an appointment. They then contact you and go through what needs to be done as far as paperwork, etc. They’ll want your insurance information, your Primary doctor info, etc. It was pretty easy for me. I did have to get the release of information to my doctor so Mayo could get all of my records. I had my CT at SimonMed (local) so I had to get them a release as well. But it was still a fairly easy process. However, I work in an office so I had the email and fax capabilities, I know thats a different situation for others.
I hope this helps. Best of Luck! God Bless you and keep you near him! Cindy
Did your Dr have to refer you to Mayos? How long did it take for you to get your second opinion there?
Didn’t know my chemo drugs have steroids. I’ll have to ask.
As much as I understand your urge to be aggressive in addressing the nodule, Becky is correct. My module increased from 9 to 14 mm in one year, but it was about as deep as it could be in the left lower lobe, and slam up against the outer wall. So the doc didn’t want to take that risky journey with a biopsy needle. We ended up deciding to just take it out.
I was referred to a Pulmonologist immediately after discovering my 1 cm nodule. It did end up being adenocarcinoma, fortunately it was caught early so no chemo or radiation. The pulmonologist will explain everything to you and keep a watchful eye. Stay positive and aggressive. Best to you!
Perhaps you might want to have a biopsy done to confirm whether or not it is or isn’t lung cancer. I have a 14 mm nodule but the lung biopsy showed aspergillosis and not lung cancer. Good luck. Irene5