Multiple lung nodules: Might they be noncancerous? What next?

Posted by felix536 @felix536, Aug 17, 2021

I have 3 lung nodules measuring 4mm, 6mm and 14 mm in three different lobes. Have had ct scans showing no change in 6 months and have another scan scheduled in three months per my pulmonologist. Should I get a second opinion from an Oncologist or wait it out? What are the chances of this being noncancerous?

Interested in more discussions like this? Go to the Lung Cancer Support Group.

I found out in Dr report I have a history of pulmonary fibrosis. No Dr ever told me that. I would've quit smoking immediately!

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Next scan in 3 months.

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@merpreb

@felix536- You are getting very sophisticated testing already. Multiple lung lesions are all primary nodules that seem to begin as ground glass. What I would love is a test that would tell if the nodules are cancerous and should be treated, so others can be left alone! I have had a slew of nodules that have come and gone, and many little thingies hanging around, just taking up space.

Will you please join us in the Multifocal group?
https://connect.mayoclinic.org/discussion/multifocal-adenocarcinoma-of-the-lung-continual-recurrences/

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PET/CT Scan. $10k test. They can see cancer areas if there are any.

I am lung RADS category 2. 5 nodules under 6 mm. Ground glass opacity upper left lobe. Scared. Long time smoker.

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@etb2

I want to thank those who commented. I don't mean to sound angry but I guess I am in a way...I wasn't told SBRT could cause bleeding cuz of the polycethemia. I was told it could just cause it a year or two after the SBRT. The polycethemia and the way I bleed would just be a complicating factor.

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@etb2- Yes, but it might not be. This might be why your doctors are taking a second look at you. But I stress, you really do need some sort of a sit down with them. It would be best if you weren't confused by what he meant by the time line.

Doctors should be giving you clear information so that you can make educated and informed decisions.

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@etb2

I want to thank those who commented. I don't mean to sound angry but I guess I am in a way...I wasn't told SBRT could cause bleeding cuz of the polycethemia. I was told it could just cause it a year or two after the SBRT. The polycethemia and the way I bleed would just be a complicating factor.

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Hello again- I've been thinking about this. I have found this so far, although you do not have prostate cancer.

https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.722852/full

The correct spelling is polychemia

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@vic83

Regarding my experience with SBRT, it is now three weeks and I have had zero side effects.
I have read that SBRT is typically between 3 to 5 sessions. In my case, they could do in three sessions in three consecutive days, maybe 20 minutes a session. My skin did not burn or even become red. I cannot tell where the radiation went. I did not notice any extra fatigue - I am still recovering from surgery in May so I deal with shortness of breath, nerve numbness.
Doctors did advise me that with radiation there is the risk of bone thinning and potential skin cancers. So, I will just be attentive for that in the future. Especially because I expect to do additional treatments for other nodules.

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We're you told anything about potential bleeding a year or 2 after the SBRT? Everything was all set...the CT Mapping...SBRT was to be in 10 treatments cuz of my tendency to bleed easily. CT Scan done in midaugust showed nodule had grown but center rescheduling called....said CT Mapping and SBRT was off....scheduled Another CT and consultation with doc....I tried to get hold of ANY medical member of my team since then....no one is contacting me back.....I don't think I'm being unreasonable to want to speak to someone about why everything has changed BEFORE I go for the CT/Consultation.

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@etb2

Non small cell lung cancer (adenocarcinoma)

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I want to thank those who commented. I don't mean to sound angry but I guess I am in a way...I wasn't told SBRT could cause bleeding cuz of the polycethemia. I was told it could just cause it a year or two after the SBRT. The polycethemia and the way I bleed would just be a complicating factor.

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@merpreb

@etb2- I'm sorry that you have had such a difficult time with your team. I've not heard of bleeding with SBRT and polycythemia vera, especially 2 years out from the radiation.

There are no incisions with this type of radiation. The radiation, the "rays" go through your skin. You feel nothing during the sessions. Nothing at all.

Did the doctor tell you the name of the cancer?

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Non small cell lung cancer (adenocarcinoma)

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@etb2

. INSTEAD, Thanks Merry, Finally, some answers! The nodule, which I'm told is located deep in the upper part of the left lung and close to blood vessels has doubled in size in the last 4 months. The CT Scan was combined with a pelvic CT ordered by my Nephrologist and read by the same radiologist, if that makes any difference. I'm just really freaked out because, since then, I haven't been able to contact ANY of my team, let alone my radiologist oncologist. What I got was several calls from scheduling telling me the CT Mapping scheduled for the 12th was off as was the SBRT. Instead I was to come in a week later, have a regular CT and a consultation with the radiation oncologist immediately after. he had told me this was the slowest growing lung cancer. He had told me I had 4 to 6 years to live if I didn't have the SBRT. I don't want to have it bcuz he said there was a rare chance that a year or two after the SBRT I could start to bleed which would be bad. Very bad for me bcuz I have polycethemia and, although my blood is thick, I usually require a trip to the ER or doctor for a few more stitches after I get home from even minor surgery. I don't know what to think. This doctor is my second opinion. But can you tell me about the bleeding a year or 2 after the SBRT? Have you heard of that.?

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@etb2- I'm sorry that you have had such a difficult time with your team. I've not heard of bleeding with SBRT and polycythemia vera, especially 2 years out from the radiation.

There are no incisions with this type of radiation. The radiation, the "rays" go through your skin. You feel nothing during the sessions. Nothing at all.

Did the doctor tell you the name of the cancer?

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@merpreb

@etb2 - Let's define "pleural-based nodule"- Nodules in the pleural cavity (the pleura includes two thin layers of tissue that protect and cushion the lungs. The inner layer (visceral pleura) wraps around the lungs and is stuck so tightly to the lungs that it cannot be peeled off. The outer layer (parietal pleura) lines the inside of the chest wall.

SBRT does not have side effects like a pill might. However, burning, such as sunburn, can take place where the rays are directed. Fatigue is a side effect and the amount of fatigue, the length of time, the number of days, and the dosage of the beams will determine how tired you will be, along with your physical stamina.

I remained fatigued for quite a while.

Your lungs will likely react with some swelling as these rays are meant to for setruction and are strong. You might have a cough bad lung irritation, or pneumonia. I did, and I had to take a strong antibiotic and prednisone for a few months.

This was my third use of SBRT. My lungs, after 25 years of treatments, are very sensitive. My reactions were rather extreme. But not having all the side effects of chemo was also a relief.

If I were you I would get a second opinion. By the way, a biopsy is seldom done with SBRT because whoever set up the regulations thought that if you are killing the cells what difference does it make if they are cancerous or not?

I haven't looked to see if you had a CT or PET. If your PET lit up then your tumors are most likely cancerous.

SBRT does have side effects.

Merry

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. INSTEAD, Thanks Merry, Finally, some answers! The nodule, which I'm told is located deep in the upper part of the left lung and close to blood vessels has doubled in size in the last 4 months. The CT Scan was combined with a pelvic CT ordered by my Nephrologist and read by the same radiologist, if that makes any difference. I'm just really freaked out because, since then, I haven't been able to contact ANY of my team, let alone my radiologist oncologist. What I got was several calls from scheduling telling me the CT Mapping scheduled for the 12th was off as was the SBRT. Instead I was to come in a week later, have a regular CT and a consultation with the radiation oncologist immediately after. he had told me this was the slowest growing lung cancer. He had told me I had 4 to 6 years to live if I didn't have the SBRT. I don't want to have it bcuz he said there was a rare chance that a year or two after the SBRT I could start to bleed which would be bad. Very bad for me bcuz I have polycethemia and, although my blood is thick, I usually require a trip to the ER or doctor for a few more stitches after I get home from even minor surgery. I don't know what to think. This doctor is my second opinion. But can you tell me about the bleeding a year or 2 after the SBRT? Have you heard of that.?

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