Anyone living long-term with DIPNECH on lungs?
I have written on this form before. I am 71 and was diagnosed with very slow growing neuroendocrine tumors on my lungs 8 years ago. No treatment at all . Two years ago I had lower left lobe removed as one small tumor changed . I saw my oncologist yesterday for my 6 month blood and scan / X-ray. I was very happy and fortunate to get a stable , no change report . My encologist said I could go on like this forever ( although I live in constant fear ). Is there anyone who has this neuroendocrine dyptic tumors that is leading a long life with little or no treatment. My only problem is I get out of breath when I climb stairs or any upgraded hill. I can live with this. Just want to know if anyone else has been living a long time with this. My doctor called this a condition I could live with rather than a cancer ( even though it is )
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
@jhhaas
Good idea to get a second opinion. Glad you don’t have coughing. Octreotide also helps my shortness of breath upon exertion and throat clearing but it does have side effects. Yes, people can live a very long time with DIPNECH since it’s slow growing. Best of luck.
My dipnech was also found by chance, I had fallen down some steps and landed on my head, was taken to hospital for a scan on my head and a tumour ( our spelling in Australia) was found in my top right lobe, another scan found a large one in my middle lobe hence me losing half my right lung and will now lose the rest of my top lobe. Pathology found the dipnech when they analysed the half lung taken 6 years ago. Shortness of breath and cough have been a problem for many years, but hey I'm still in the land of the living and grateful for it. Good luck too
I have also been diagnosed with DIPNECH and have probably had for 20 years. I have 20 tumorlets spread on both lungs. My cough became chronic and unbearable three years ago. What are the side effects from octreotide? Have you lost your hair or has it thinned?
Hi. What side effects do u have from the injections? Please advise.
Thanks!
Hair thinning, fatigue, low blood pressure and heart rate, blood sugar spikes. I also started breast cancer meds that cause hair thinning and fatigue just two months before I started octreotide so it’s hard to know how much each med is responsible for. The side effects from octreotide are much better than the chronic coughing, mucous and shortness of breath that it alleviated so I don’t plan to stop octreotide as long as it’s effective.
Is this type of cancer considered Merkel cell carcinoma as well? I was reading about Merkel cell carcinoma and I click the link and it brought me here to you.
I took immunotherapy I was diagnosed in June of 23 with Merkel cell carcinoma it was in both sides of my neck and all my lymph nodes and I took immunotherapy and I just finished my treatment after one year I run the Bell and in the last PET Scan they told me that my loan was inflamed and they wanted to do an MRI or CAT scan and they did that last week and they found it in my lung. So I was just doing a little bit of research to see how long I might live because they're not telling me anything and here I am with you on for some reason so I just wondered after reading about your story if yours was Merkel cell too thanks for your time
Hi @donnapeck51
I’m sorry to hear about your Merkel cell carcinoma. I’m not a doctor but from what I’ve read Merkel cell carcinoma is a rare neuroendocrine skin cancer. Is that your understanding? So now they are saying the Merkel cell is in your lungs? Have they done a biopsy to see if that’s Merkel cell in your lungs or possibly something else? Are you seeing a NETs team? You need Merkel cell/NETs specialists who can answer your questions.
As for DIPNECH, it is even rarer and originates and stays in the lungs. It presents as multiple slow growing nodules and respiratory symptoms. It’s pre-cancer but can progress to lung carcinoids/NETs that is cancerous. I do not believe DIPNECH is Merkel cell but they are both neuroendocrine disorders. I hope that helps.
@donnapeck51
I just did a search for Merkel cell on this Mayo patient site and there are discussions about it. Use the search tool and hopefully someone else with Merkel Cell can be of more help. One of the Mayo monitors will likely add a note here soon to steer you in the right direction. Prayers for you.