Is a Spiculated lung nodule always malignant?
Hello,
58M, Nonsmoker, No history of cancer
I went to a pulmonologist due to coughing, shortness of breath for over 2 years and got diagnosed with allergic asthma.
Ct scan showed 5 lung nodules all on the right lung.
2 are calcified -most likely granuloma,
2 perifissual- which are most likely benign
1 subpleural nodule 5mm
1 spiculated nodule 5mm
The spiculated lung nodule worries me the most
I did research and all data and studies say that spiculated nodules are malignant with a predictive value of up to 90% ..
Doctor wants to just monitor it with follow up Ct scans.
I read that in rare cases infections, Inflammation or sarcoidosis can have Spiculation but Generally such nodules are a sure sign of Malignancy.
Anoyone on here who has experience ?
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No lymph nodes lit up. The PET scan was 4 months ago. The dominant is in lower right lobe, the subpleural one is lateral lower right lobe. Its behind a rib and cant be accessed with needle aspiration. The ground glass one is along the periphery of the right lower lobe. The dominant one was apparently part cystic and part solid. The cystic part of that nodule has actually "slightly decreased" but the solid part has not.
@darwin66 , I'm not sure that I would be comfortable with a long wait-and-see period. Each patient's tolerance for risk is different. I tend to be more analytical and want data and facts. Have you been able to have a PET scan to see how much uptake there might be to the nodule? Are you able to access second opinion?
@shellyrenee, With the symptoms that you are having, and the CT and PET results, you certainly sound like you need treatment. The weight loss and the rib pain are certainly concerning as well.
Are you being seen at a medical institution that sees many cases like yours, or is it a smaller local clinic/hospital? Most experts will urge patients to be seen at a teaching hospital, or one specializing in cancer, or even specializing in thoracic oncology.
Waiting can be so hard on us, the emotions of not knowing the next steps can be overwhelming. Is it possible for you to get on a wait list for an earlier appointment with the surgeon?
Wow. That really doesn't seem right. With a size of 2.8x1.8x2.2 cm, they should have acted right away and performed a biopsy, especially if the lung nodule had spiculated characteristics. In addition to the increased SUV uptake and your symptoms, they should not have waited at all. It’s always about early detection, but when they find suspicious findings, they still expect us to just wait and do nothing. I bet if they themselves were affected with such findings, they wouldn't be so careless and would be much more proactive.
I have another CT with contrast this Friday and the earliest the surgeon could see me after that was on the 28th. Im being seen at Vidant Medical Center in Greenville, NC. I will let them do what they are going to do (unless the surgeon tries to push it off any further), but my fiancé' and I have already decided that if it is cancer, I will not stay with the hospitals in NC. I will be heading to the Massey Cancer Center At VCU in Virginia.
I agree, 100%.
Let me say, they did a fine needle aspiration on one of the nodules. But here is my concern with that, even though it came back negative for malignancy. I dont trust it. The chances of false negative are higher than we know, with FNA. Also, it was sent to ONE pathologist, right there at the hospital that the biopsy was done at and the result was back in 1 day. When my daughter was diagnosed, it was sent to 4 major cancer hospital pathology labs. I could go on and on about "false negatives" and their impact on the patient after a second biopsy was done and came back malignant. And all of these were on people I personally know. So not just something Im reading on a website that happened to someone I dont know. I know every one of these people. Thank GOD, they advocated for themselves, because every single one of them came back as cancers. Breast, rare uterine, prostate, etc. Cancer is very rampant in my family as well. Lung, stomach, colon, bladder, kidney and my daughter had non Hodgkin's lymphoma.
Its just wild.... I finally told my pulmonologist to think of me as his mother, sister, wife and asked him what would he be doing different at this point. I am 49 years old. On oxygen and having these issues. I have grandkids. And yes, the not knowing is reeking havoc on my mental health. Some kind of bad.
I will get a second opinion soon and ask about removal options. Unfortunately, many doctors don't take our concerns seriously and are not willing to take our wishes to account . The PET scan was already declined by my previous doctor, as it apparently won't show meaningful results for nodules under 1cm. However, I believe it would still be beneficial to have the scan to potentially rule out metastatic disease or other suspicious findings.
It's very frustrating and hope for better care with the new doctor.
I hope you get that too!!
Its almost like (with a lot of doctors) if we dont fit the text book material, then there is nothing wrong with us. Im thankful for the "book sense" of doctors, but I feel like they could use a little more common sense as well. Every situation is different. And just because a book says that it MUST be benign if this happens or that happens.... doesnt make it true. Look into it!! Find the root cause. Find the diagnosis and find the treatment. For our mental health's sake.
My daughter was diagnosed at the age of 6 months old and she was the first baby to EVER be diagnosed with they type of cancer. T-cell lymphoma (non Hodgkin's) It is a cancer that "typically" occurs in adults over the age of 40.
Good luck to you!!! I hope you find the answers you need and I hope they are good ones.
@darwin66, I know you are actively advocating for yourself. Just a note, My initial PET at the time of diagnosis did show obvious cancer in my lymph nodes and lung, but there was also just a tiny spot on my liver that was lighting up too. That wasn't noted in the radiologist report, but the pulmonologist saw it when he was reviewing the scans prior to a bronchoscopy. They did a liver biopsy, and it was metastasis from the lung. It was certainly under 1 cm in size, and it showed up on the PET. That forced me to stage IV, and drastically changed my treatment plan. I'm glad the pulmonologist picked up on it.
Hi @shellyrenee, I know that you are the only one that can make decisions for your own care, and I'm sure this is very overwhelming. Based on what you've shared with us, you may want to consider a call to Massey now. They are a National Cancer Institute site, and well respected. Massey may recommend a different treatment than the surgeon at your local hospital. A second opinion prior to any surgery may be invaluable in your case.
You mentioned that you are fairly young for lung cancer. There are more and more young(ish) people being diagnosed with lung cancers that are caused by gene mutations (ALK, EGFR, KRAS). IF cancerous cells are found, please ask about "biomarker testing" where they will look for what's driving the cancer.
I (a never-smoker) was diagnosed at 49 with one of these mutations. My treatment was very different than the traditional surgery/chemo/radiation route because we found the biomarker that was driving the cancer.
I'm so sorry to hear about your daughter too. It's so hard to wrap your mind around cancer, but cancer in children or babies is even more difficult.