← Return to Diagnosed with Ameloblastoma
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Replies to "Hi Tom, good luck with your targeted treatment. Here is my story: I was recently diagnosed..."
Thanks for sharing... Really appreciate it. Long journey to recover... I feel nervous to wait for my daughter resection next month, she's only 14... diagnosed with unicystic ameloblastoma. Next month the OMFS will do the marginal resection and after 6 month they will do the reconstruction...
It's really helpful when reading your experienced and situation... Get well soon @kkd
-We lived in Menlo Park and I worked as a nurse at Stanford for over 20 years, about 20 years ago. Still have lots of friends in the area.
-Does Stanford have a team that routinely performs ameloblastoma surgery/reconstruction? -My son (23 years old living in Orlando, FL), had oral surgeon remove a mandible jaw "cyst" in August 2023. They said no biopsy needed, they would just take out the whole thing. Pathology report came back with ameloblastoma. Now after 3 months healing he just saw head and neck surgeon (Fawaz Makki) in Orlando who operates at an Advent Health hospital nearby. The newest CT shows they didn't get it all. (No surprise there.)
-I've looked at Stanford but cannot tell if they perform the surgery with fibula FF often and if they have a team approach to the surgery/post-op recovery--nurses on the post-op floor familiar with care, PT familiar with the fibula surgery and know what kind of care/exercises are needed, etc. We live in Rochester, NY--so will most likely have to fly wherever we go for surgery. Mayo is definitely on our list of options but need to know more about Stanford before getting a 2nd opinion there. Who were your surgeons? Do you know how often they perform this surgery?
_Thank you in advance and continued success with your recovery.
Annie
@kkd Wow, that sounds really, really rough.
Best of luck on your recovery. You're the first person I've heard from with a maxillary ameloblastoma.
It does not surprise me your tumor didn't have the BRAF V600E mutation - from what I could find in the literature, that mutation shows up in somewhere around 80% of mandibular ameloblastomas, and is rarely if ever seen in maxillary ameloblastomas.