Anyone had surgery to remove typical carcinoids of the lung?

Thank you for all the information. I will definitely look into those sites.
I am 72. The carcinoids are at the top of the lower right lobe. That is why he has to take the whole lobe.
I never heard of what you have.
Do you have a lot of follow up scans?
I have a great team of Doctors at Emory University Hospital.

I opted to not have the surgery because I would be on oxygen the rest of my life. I did a natural healing process, and my NET decreased in size in June, from December. I have another cat scan soon, so we will see where we go from there.

If anyone out there can recommend a Dr. in the Florida area that is very familiar with treating Dipnech. I am under a pulmonologist care now for many years and now i would like to see a specialist in this field.
Thank you

@mcohan
Most doctors, even radiologists, pulmonologists and oncologists haven't even heard of DIPNECH. I recently went to a cancer talk and asked the lead thoracic surgeon at the hospital if he was familiar with lung NETs. He said yes. I asked about if he's heard of DIPNECH and he said no. I gave him and overview and asked him to spread the word.

DIPNECH is rare with only a couple hundred diagnosed cases, but they think it's underdiagnosed. Mine went undiagnosed for 12 years after a CT spotted 50+ tumors. At least 20 specialists had incorrect guesses. We monitored with CT scans for awhile and all the tumors were very slow growing. I finally stopped that because of radiation exposure, but then when I was diagnosed with recurrent breast cancer, they really pushed for the lung biopsy. I hadn't let them biopsy for 12 years because I wasn't going to let them cut my chest wide open when a lot of specialists were guessing it was something benign. But after 12 years, they had grown enough that they could do a needle biopsy. After lung NETs was diagnosed from the biopsy, I started reading up on that and couldn't figure out why people usually had one tumor yet I had so many. Through my own research, I came across a Mayo Clinic retro study on DIPNECH patients -- aha! I was sure that was it. My breast oncologist had never heard of it. I asked for a referral to the UCLA NETs multidisciplinary team and they were familiar and confirmed that's what I have in addition to lung NETs.

DIPNECH can also cause hypoxia (low blood oxygen levels). My resting oxygen level based on my pulse oximeter is 92-93%. I only started monitoring when the pandemic hit so it may have been low for years and years. For two months straight recently it was 90-91% with dips to 88-89%, but then went back to 92-93%. Mystery. It's lowest when I'm in the recliner (even just slightly reclined) or in bed. I lied down flat at the pulmonologist's office to show him and yep, 93% just like I said. If I'm sitting in a desk chair, it's 96%. It will go higher if I'm up moving around. So weird and not good for my body or brain, but he said insurance only covers oxygen if lower than 88% even though 95-99% is considered the normal range.

I have CT scans every 6 months to monitor my lung NETs, DIPNECH and advanced breast cancer. I do it all at once to minimize radiation. DIPNECH is very slow growing, but often very symptomatic. DIPNECH is typically diagnosed in middle-aged non-smoking women in their 50s-60s who have a long history of coughing and shortness of breath that has been misdiagnosed as asthma, COPD, etc. Note that I also have had asthma and allergies from the day I was born, but it turns out DIPNECH really added insult to injury. I now know that due to the improvement with the octreotide treatments.

@meryls12
Since Mayo Clinic was the first to do a big study on DIPNECH, that should be a good place to go. Florida is large so I'm not sure how close you are to Mayo. Robert Ramirez DO at Vanderbilt University in Nashville has done more talks on DIPNECH than any other NETs specialist I'm familiar with. If I ever feel I need a second opinion on DIPNECH, he's the one I plan to contact. Right now, I feel like my UCLA NETs team is on top of it. In fact, my IR said he's seen 14 patients with DIPNECH. That's a lot considering how rare it is.

You could probably do a video consult with Dr. Ramirez if you send him your records. The first link is the latest talk on DIPNECH by Robert Ramirez 11 months ago. The second link is was his talk 3 years ago. Very informative. Most NETs talks just mention DIPNECH briefly or not at all.

You'll hear in the talk that some people can eventually need a lung transplant from blocked airways, but from what I've read, it seems that is not typical. Again, I think it's just starting to get more attention and data because they believe it's underdiagnosed. My IR told me there just isn't enough data on it yet to make good predictions for me, but he expects we'll be long term partners in this. The talks are worth watching if you have or think you have DIPNECH. I hope this helps. There is a new study going on right now though.

This is not typical or much related, but after my bronchoscopy and suffering a month of bacterial pneumonia, I feel what hasn't taken me in 75 yrs and has been there over 50yrs can remain.

@woundedwarrior1969
Your philosophy certainly may be true for some disorders. In the case of DIPNECH the symptoms have to be managed as they can really diminish your quality of life as they did in my case for 30 years not to mention annoyed the people around me. In the case of lung NETs, the cancer can metastasize and then you have even more problems, harsh treatments and rough surgeries coming your way not to mention life threatening. That's why they destroyed my largest lung tumor (2.6 cm) and told me any others that reach 2 cm have to go. Unfortunately, we can't just ignore these two conditions without regret.

I also believe as you get older you may start playing the odds on what will get your first. Even though I'm only 64, I also have advanced breast cancer so I sometimes ignore other disorders because I think the breast cancer will take me first so why bother with x, y and z. I even have doctors tell me that. Believe me, I love ignoring health issues whenever possible and often feel the cure can be as bad as the illness. I understand your thought process, but everything medical is on a case-by-case basis. I hope I'm around to celebrate your 100th birthday with you. 🙂

Thanks, I'll review my thoughts at years end.

@meryls12, you may wish to consult with the leading NETs team at Mayo Clinic in Jacksonville who have experience treating diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH).

Here is the link to get started, if you wish to inquire about a second opinion http://mayocl.in/1mtmR63

Thank you so much for this information, I really appreciate it. Hope your doing well.

Hi - I’m new here. But I saw your question. I was diagnosed this summer with a malignant lung nodule, found incidentally. Had right middle lobe removed at Sloan Kettering, eight weeks ago done robotically and recovering well. Testing revealed the malignant tumor was typical carcinoid, and that I have DIPNECH. I will get scanned every six months at Sloan Kettering, but my surgeon says there is no other treatment needed right now, and referred me to a local pulmonologist. The lobe that was removed revealed other nodules that were not yet malignant. And scans show there are lumps and nodule on my left lung. I’m just trying to find out if there’s something else I need to be doing in terms of prevention or treatment. The local pulmonologist was not familiar with DIP NECH. If you opt for surgery, I can’t emphasize enough how important it is to go to the very best doctor and team that you can find. I was so happy with my treatment at Memorial Sloane Kettering. FYI, I’m a 74-year-old, active female.