Hi, sorry for your diagnosis, how are you going now an update of how you’ve been for last 8 or so years if this thread is still active? Did you ever find out which hpv strain caused the nasal papilloma? My strain has never been confirmed but only picked up through the new hpv Pap smears screening that came out last year in my state. I have not had any visible complications to date but uncomfortable symtpoms which cannot be explained and only a diagnosis of high risk
I'm 28 years old. I was originally diagnosed with IP at 17 years old. Over the span of 11 years, I've had 5 surgeries: one was a biopsy alone, the endoscope resection, then another endoscopic resection and lux Caldwell incision. After that surgery, I had no recurrence for 6 years. I then had a recurrence and surgery in April of this hear and was just told in June it has come back again in a very small place. Being that my condition is benign with no sign of malignancy or dysplasia, my ENT reccomened we moniter it's growth for 3 months. I plan to undergo anther surgery at that point and hopefully I have no recurrences. If anyone has any questions or needs any support with thus condition feel free to email me at ***@****. There is very little info online so you may find my insight helpful.
What were your symptoms at the original diagnosis.
I had my 2nd surgery to remove IP from my right nasal sinuses. They took pieces of sinus and bone out to go after the root, but they also noticed some growth that was too close to my brain to remove using endoscopic surgery. I'll have an MRI in about 6 months to re-check, and may have to have major surgery (i.e., cut open my face to get at it). Not looking forward to it, to say the least.
Can IP be caused by oral sex with a woman who has HPV? Is it hereditary? I have no idea.
I just stumbled upon this thread while searching for general IP info. I'm 25, and my (left side) nasal IP was diagnosed/discovered in 2003 when I was 17. It's been partially removed twice, and my third surgery in seven years is tomorrow morning. My previous ENT doctor told me that total removal was impossible -- which is, apparently, untrue. My new ENT intends to remove it totally, though this does involve removal of part of the lower concha, and some skin (which the IP has grown against).
Regarding treatment, both surgeries have been partial resections done endoscopically. Tomorrow's surgery will be endoscopic as well, but we're aiming for total removal.
No one's sure what causes IP, though the prevailing thought is, of course, that it's caused by a strain of HPV -- though what triggers it into action/growth is unknown, as is, insofar as I know, what strain causes it or how said strain is transmitted.
Anyway, I hope your second surgery went well and that you haven't had a recurrence.
Thanks for your input. I have CT scan tomorrow and see surgeon next Monday. I will let you know what I find out.
I'm not sure you'll find much experience here, I seem to be the only respiratory papilloma sufferer right now. There is, however a great wealth of support and collective knowledge, so keep posting and please share what you learn.
From the American journal of Oncology.........
The preferred treatment of inverted papilloma is surgery; postoperative radiotherapy is added if it is associated with squamous cell carcinoma. The likelihood of local recurrence after surgery for inverted papilloma may be substantial and varies with the extent of resection.