NET - Insulinoma
Hello to All,
I am joining this group from the Diabetes/Endocrine group. In July 2015 I was diagnosed with 2 insulinomas - both removed surgically at DUMC in NC. The diagnostic work-up included a 5 day hospital stay (72 hour fast + complications) and the surgery was an 11 day hospital stay (typical stay for a Whipple procedure). About 3 months post surgery, I started having recurrent hypoglycemia symptoms very similar to my pre-op symptoms. Insulinomas are very difficult to diagnose and locate and so far they have not been able to locate a new tumor but do suspect there is regrowth of an old tumor or growth of a new one. That is what will bring me to Mayo next week. Anyone been through insulinoma testing at Mayo? Hopeful to be starting down a path to possibly find a resolution of daily hypoglycemia symptoms but nervous because I have walked down this path once already. Glad to see the new group on NETs. Thanks.
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Hello @nancymcegg and welcome to Mayo Connect.
I am so sorry to hear of your possible insulinoma diagnosis. I can certainly understand your concern, especially when two different doctors give you different answers. Is it possible for you to get a second opinion at Mayo. They do have a facility in Florida as well as Arizona and Minnesota.
Will you post again and let me know how you are doing?
Do you know of a specific doctor I should make an appointment with at the Mayo in Florida?
Hello @nancymcegg
No, I am not familiar with the NET specialists in Florida, but if you call Mayo's Florida appointment desk and explain that you need a second opinion for a possible insulinoma diagnosis, they will undoubtedly know who you should see. Here is their number for scheduling appointments at their Florida location:
Mayo Clinic in Florida
727-369-6849
8 a.m. to 5 p.m. Eastern time, Monday through Friday
Will you post again and let me know how you are doing with your second opinion?
Hi @amya
I was noticing that in your post last month you mentioned a Mayo appointment Oct. 18 to the 24th for testing about insulinoma. I hope that appointment went well and you received some answers.
If you are comfortable doing so, will you update me on how you are doing?
Hello @nancymcegg
I was just thinking about your last post or Oct. 3 and I hope you are feeling better. I was also wondering if you have any answers regarding the possible insulinoma diagnosis.
Have you gotten another opinion at Mayo or another facility yet?
Mayo was able to confirm diagnosis of insulinoma and find it with endoscopic ultrasound. Everyone was wonderful. Kind, compassionate and knowledgeable. I am scheduled for surgical removal on 11/27. I am confident in the care I will receive. My worries now are centered around insurance coverage. Working with them to try to get the needed documentation. Sounds like they will approve the insulinoma removal at reasonable and customary. I will need to cover costs above this. I was advised to have my gall bladder removed. I may have to do this in a separate surgery at home.
I am so glad to hear that you have a confirmed diagnosis and a treatment plan in place, @amya. That is a relief, isn't it? I will certainly pray and send good thoughts your way on 11/27.
While I have not been diagnosed with insulinoma I have had 3 surgeries for NETs in the duodenal bulb and the 2nd surgery included the removal of the gallbladder. That procedure seems to be common with NETs patients, but I'm not sure of the reason for that.
Do you know how long you will be hospitalized after surgery?
It is a relief. I'm a bit hung up the logistics of the financials, but the tumor must come out. I'll deal the the financials as I have to. I'll be in the hospital for about 5 nights they predict. Will depend if they can do it laproscopic or have to convert to open. I hope you are feeling well.
This all sounds good, @amya. I'm sure you will be relieved to have this over. The laparoscopic sounds interesting. I wasn't aware that type of surgery could be done that way.
By the way, was the Gallium 68 Pet scan used to diagnose your insulinoma?
No. They started with CT, didn't find. Endoscopic ultrasound found it. If it didn't they were going to do a calcium stimulation test.