I am 75 and have carcinoid tumors NET in lungs

Posted by ggiinnaa @ggiinnaa, Apr 18, 2025

One doctor suggested that I have DIPNECH I do have small carcinoids throughout my lungs. They were discovered when an Adenocarcinoma and my top right lung lobe was removed. I would love to hear from anyone with DIPNECH or carcinoid lung NET

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

Profile picture for sadragliz @sadragliz

I also have NET and DIPNECH. Both were found in August of 2024 when my tumor in my lung was removed. I never had a cough but have always had to clear my throat. I am given a blood test every 3 months and CT every 3 months after that. So far I have two very small spots on my right lung that we are watching for any changes. My left lung is where my surgery was. So far no carcinoids either. Wish there was more info on DIPNECH, as sad as it sounds, I am glad I am not alone in this journey. I am of polish decent. God Bless you all.

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I wish you the best. Please keep us posted. It helps me a lot knowing there are others. I never smoked and letting friends know I had lung cancer was difficult. Thank you

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Profile picture for ggiinnaa @ggiinnaa

I wish you the best. Please keep us posted. It helps me a lot knowing there are others. I never smoked and letting friends know I had lung cancer was difficult. Thank you

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Typical carcinoids and DIPNECH are not associated with smoking. The majority of cases are non-smokers and for those that smoked it’s unrelated. Terrible that we feel we need to defend ourselves from judgement. My brother had the most common type of lung cancer (NSCLC) and never smoked a day in his life, never drank, always exercised. He was fit and healthy. Died at 48. Same with my colleague who died at 50. Even for those who did get some type of cancer from smoking, heart disease from poor health habits, etc., we shouldn’t think they deserve it. We’ve all made some bad choices along the way. Mine is catering to my sweet tooth.

Luckily for us, typical carcinoids and DIPNECH are both very, very slow growing and treatable. We may outlive our doctors!

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Profile picture for Zebra @californiazebra

@sadragliz
Welcome to the DIPNECH club. Are you being followed by a NETs team?

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No I am not. My pathology after my lung surgery was sent to Mayo, and that is how I got my results for NET and DIPNECH. No sure if there are NET Teams in Illinois.

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I had my lower right lobe wedged last July. It was suggested that I see a surgeon who is a specialist in carcinoid tumors, and found one in Portland, Ore. at OSHU. This doctor thinks I have DIPNECH as well. My problem right now (8 months out) is horrible pain at surgery site. The nets specialist said the surgeon who removed the tumor should not have used a robot as I am a fairly small person. He said he would have #1 waited to see if it would have continued growing, then #2 would have operated the old fashion way. He is saying my pain is called PFT, having to do with nerve and muscle damage. I have had one round of shots in my back to detect where the pain is radiating from. They did not capture it, so I am going to have to have a second try before they can do an ablation. Is anyone else dealing with on going pain after surgery?

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Profile picture for jhhaas @jhhaas

Hi - I am also 75 and have DIPNECH, diagnosed Oct 2023 when I had my right middle lobe removed. I had 2 “carcinoid” tumors in that line and PET scan showed one had malignancy. Testing showed they were “typical carcinoid“ now they mostly just call them. NETs. My other lobes all have lumps and bumps and some other small tumorlets. There was no lymph node involvement, and I currently don’t get any treatment, just scan and see the doctor every six months. So far it has remained stable, but next week I go for my next scan. My main symptom is shortness of breath on exertion, like if I walk too fast or try to climb stairs or hills. I also learned that.GERD can be part of it, and I have been on medication for that for many years. I guess now I know why! Many people with DIPNECH have problematic coughs. I don’t have that, but I do tend to clear my throat often throughout the day. I’ve been getting allergy shots for many years, thinking allergies are what was causing what used to be chronic chest infections and coughs. That has kept me from having any more bad coughs or even colds and flu! They currently don’t take treatment for DIPNECH, my doctor does not feel it is needed at this point. I do plan on getting a second opinion at some point from another NET specialist but at this point, I’m doing pretty well. Wishing you all the best.

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@jhhaas I'm just wondering, if you have multiple nets throughout your lungs, why your doctor did not feel Octreotide was the next step. I have 3 more very small tumors in my lungs, and my doctor said the injects could help keep them from growing (?) I am waiting to be able to go back to work and I am worried about the side effects of Octreotide.

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Profile picture for nannybb @nannybb

@jhhaas I'm just wondering, if you have multiple nets throughout your lungs, why your doctor did not feel Octreotide was the next step. I have 3 more very small tumors in my lungs, and my doctor said the injects could help keep them from growing (?) I am waiting to be able to go back to work and I am worried about the side effects of Octreotide.

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@nannybb I think it’s because I don’t have too many bad symptoms at this point. I do not have the cough that many have, but I do get scanned every six months so if there’s any changes then that would be a possibility. The doctor was my surgeon at Sloan, where I went for a second opinion, and he immediately suspected correctly what it turned out to be. So he does the follow ups to make sure it has stayed the same, but he referred me to a local pulmonologist. However, that doctor doesn’t know much about it. Right now I figure because my symptoms are not so bad, I’m OK with no treatment because I know with treatment comes potential side effects. If it progresses or things start to change, I’m sure he will refer me. I have thought about getting a second opinion with a net specialist in Philly but I have not done that yet. He tells me to go live my life and that I am very lucky so far. I am also older, 76, so maybe that factors into it as well? I don’t know. But so far so good.

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Profile picture for nannybb @nannybb

I had my lower right lobe wedged last July. It was suggested that I see a surgeon who is a specialist in carcinoid tumors, and found one in Portland, Ore. at OSHU. This doctor thinks I have DIPNECH as well. My problem right now (8 months out) is horrible pain at surgery site. The nets specialist said the surgeon who removed the tumor should not have used a robot as I am a fairly small person. He said he would have #1 waited to see if it would have continued growing, then #2 would have operated the old fashion way. He is saying my pain is called PFT, having to do with nerve and muscle damage. I have had one round of shots in my back to detect where the pain is radiating from. They did not capture it, so I am going to have to have a second try before they can do an ablation. Is anyone else dealing with on going pain after surgery?

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I also have dipnech , several carcinoid tumors on my lung. I had robotic surgery almost 3 years ago to remove a tumor that was growing. I had serious pain from the surgery for a long time . As a woman , I could not wear a bra for close to a year. It took a good two years for the pain to ease up. I was also told nerve damage. Be patient, the pain eventually goes away.

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Profile picture for rogo @rogo

I also have dipnech , several carcinoid tumors on my lung. I had robotic surgery almost 3 years ago to remove a tumor that was growing. I had serious pain from the surgery for a long time . As a woman , I could not wear a bra for close to a year. It took a good two years for the pain to ease up. I was also told nerve damage. Be patient, the pain eventually goes away.

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@rogo So you never got a nerve block to try to get rid of the pain? I am trying to go back to work and this has been the only thing I've been offered, well, besides getting injections to stop the growth of the other tumors. I asked my surgeon yesterday to please do bloodwork for baseline on all the areas of my body the medicine from the shot might effect...like my gallbladder. I was told he typically does not do that. I really don't want to complicate things, but I feel like I have little choice in my treatment plan.

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Profile picture for Zebra @californiazebra

Typical carcinoids and DIPNECH are not associated with smoking. The majority of cases are non-smokers and for those that smoked it’s unrelated. Terrible that we feel we need to defend ourselves from judgement. My brother had the most common type of lung cancer (NSCLC) and never smoked a day in his life, never drank, always exercised. He was fit and healthy. Died at 48. Same with my colleague who died at 50. Even for those who did get some type of cancer from smoking, heart disease from poor health habits, etc., we shouldn’t think they deserve it. We’ve all made some bad choices along the way. Mine is catering to my sweet tooth.

Luckily for us, typical carcinoids and DIPNECH are both very, very slow growing and treatable. We may outlive our doctors!

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@californiazebra I find it amazing that some people can be smokers their whole lives practically, and never get cancer. I don't judge them either. I know everyone has cancer cells in their bodies. It's just a matter whether they overtake good cells. Sometimes, it just seems unfair when you try to do all the right things to prevent a problem.

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Profile picture for rogo @rogo

I also have dipnech , several carcinoid tumors on my lung. I had robotic surgery almost 3 years ago to remove a tumor that was growing. I had serious pain from the surgery for a long time . As a woman , I could not wear a bra for close to a year. It took a good two years for the pain to ease up. I was also told nerve damage. Be patient, the pain eventually goes away.

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@rogo By the way, the bra comment is the same in my case. I've tried to wear a sports bra, or just go without for the most part. But I know that is part of my pain issue. Seems like they could have entered the site just a bit lower on the chest to avoid this from being a problem. 🤦‍♀️

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