I am 75 and have carcinoid tumors NET in lungs
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
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@tomrennie I’ve had these tumors show up on scans for the last 11 years and been misdiagnosed until a radiologist at Flagstaff Medical Center alerted my ER Dr of his suspicions. I know first hand that a good radiologist is key to a good diagnosis, and yes we’re only human so mistakes are inevitable. I love that Mayo is fantastic at quickly uploading your test results to the portal, unfortunately I had my erroneous results in my head for 2 weeks until I got clarification from my Dr. I had already gone back and compared it to my prior CT reports and was pretty worried that I had developed a 27mm tumor in 3 months! Occasionally you get information that you’re really not prepared to deal with, biopsy results, lab work etc and you need to grin and bear it until your next appointment.
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2 Reactions@azrosegold
Sorry to hear that. I know how stressful that can be. I recently had a radiologist make a typo on an MRI MRCP report for my pancreas, he put cm instead of mm. I even asked the NP if that was a typo because cm meant pancreatic cancer (huge) and mm was normal. She kept on with the story even though the GI team knew immediately it didn’t make sense. So I thought I was dying for 6 weeks until the GI told me it was a typo right before the endoscopic ultrasound that had completely normal results. Not okay to let me believe that for so long to cover an error.
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2 Reactions@azrosegold
Are these surveillance CT Scans
Are they with contrast
and of the Chest only. After
Surgery Surveillance protocol
seem to be different
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2 Reactions@azrosegold I understand. I had a typo on a scan report. I had a liver lesion presented at 8.6cm and not 5.6cm on the report. Fortunately, the oncologist corrected everything the next day at my appointment. Waiting two weeks is a long time. Though easier said than done, I try to not get too up or down until I meet the ologist that ordered the test. If there is more than a day between results and meeting with the ologist, I will send a message on the portal with my concerns. I have received responses back to alleviate my fears.
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1 Reaction@jhhaas My surgeon and I talked about the possible side effects of being on the shots for NETs. He told me it is common to have problems with your gallbladder. I asked what happens then? He said, laughing, "I'll just remove it." I told my GP of that interaction, and SHE laughed and said, " That's just how surgeons think." I have had over 11 surgeries in my lifetime. I'm definitely going out of this world with less "inside" than I came into this world with. 🤣
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3 Reactions@nannybb. Oh, that’s rich! Lol. But good information, so thank you for that! Ha ha. I just today got the results for my six month CT scan, 2 1/2 years postop, and so far my DIPNECH remains unchanged. So I’m not rushing into any treatment at this point.
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2 Reactions@jhhaas Good for you! I bet THAT was a relief. Since my operation in July of last year, I have not had any CAT scans done. I'm definitely bringing it up in my next visit. I too was told it should be a CAT every 3 months for the first year, than once a year thereafter. Makes me nervous....but I am on the miraculous shot. ....3 times a day self administered. Breast cancer runs in my family. I thought for sure if I were to get cancer, it would have been in that form. I read up on the type my grandmother and mother had, and it turns out it is a form of NETs. I'm getting a mammogram the first of June. Just another thing to bring up.
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1 Reaction@tomrennie A typo? That must have boosted your confidence. So glad they caught it. Shows once again, why it's a good thing to have a NETs team, not just a surgeon.
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2 Reactions@azrosegoldjust wondering.... Flagstaff in Florida? I was told in July after a bone scan that the tumor in my chest was growing. I'm sure my mouth fell to the floor. My heart did. I was never told I even had a tumor to be worried about. Now I'M wondering how long it was there. Then on my post-op visit, the surgeon told me I had 3 more. He said not to worry they were small. That was not the point. I wanted to know after having a PET scan with no more tumors found, how they suddenly appeared 2 months later? Just makes you wonder. Then I switched surgeons and was told about DIPNECH, and the shots for it. I am supposing the first surgeon did not know about either. So important to go to a specialist for Carcinoid cancer. Just because they are a "Cancer surgeon" does not mean they are familiar with the protocol for NETs.
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1 Reaction@jhhaas Wondering, did you have pain after your surgery that lasted more than 6 weeks?