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#29553 11-06-2007 08:49 AM
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Sorry I posted in the wrong spot. I am new.

I went to the dentist last week and they saw white spots where my wisdom teeth were taken out (15 yrs ago). They said it didn't look good but they would wait and see until my next visit (3 months). Should I see someone else?

#29554 11-06-2007 02:16 PM
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Absoutely!!!!!

I would not wait. Have you read on here how fast this stuff can spread? My eyes were opened when I found this site. I would take no chances. An ENT may be a good choice.

Better safe now than sorry later.


South Louisiana - Cancerous growth removed from lip 10/07. Lesion removal & biopsy done 11/7/07 - no signs of cancer in area. PET scan done. No signs of cancer in Head & neck. Something in chest. CT to be done 12/20/07
#29555 11-06-2007 02:40 PM
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K--PLEASE do not wait 3 months! If you can see it with your eyes, they can test it somehow. There are all sorts of biopsy methods available. I have had part of my hard palate removed, along with my right maxilla (upper jaw and teeth) because my dentist did not recognize my cancer and it was allowed to continue to grow for months. He did not give me cancer, but my surgery would have been less destructive if he had A. recognized it and B. moved faster in diagnosing it.

Please don't wait. Go to an ENT immediately, and even better, go to the Head and Neck department of a cancer center, where they see lots and lots of this. They will give you an appointment quickly, and with the proper specialist, likely one of their ENT's.


Colleen--T-2N0M0 SCC dx'd 12/28/05...Hemi-maxillectomy, partial palatectomy, neck dissection 1/4/06....clear margins, neg. nodes....no radiation, no chemo....Cancer-free at 4 years!
#29556 11-06-2007 02:45 PM
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question: white spots on both sides of your mouth? That would be somewhat encouraging, since it would be doubtful that cancer would occur in both places simultaneously.

You need to look in there with several mirrors and note what it looks like for yourself. And then look every day to see if it gets better or worse. If it gets better, that will be good news. If it just sits there, or gets larger, then that's not such good news, but it still might have an explanation other than cancer. The only way to know is to go to see an ENT and let him/her get an early look.

I use an old-fashioned cheap shaving mirror...on a wire stand, with a mag. side and a reg. side...I place that on the table. I have a small, bright flashlight, and another small rectangular mirror (a purse=sized makeup mirror) I hold the light in one hand, and the small mirror in the other, and I get a really good look in the magnifying mirror. Let your wife (?) look too, so you'll have another set of eyes at work, and so that she will be involved from the beginning.


Colleen--T-2N0M0 SCC dx'd 12/28/05...Hemi-maxillectomy, partial palatectomy, neck dissection 1/4/06....clear margins, neg. nodes....no radiation, no chemo....Cancer-free at 4 years!
#29557 11-06-2007 02:53 PM
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My husband's dentist noticed a leukoplakia (white patch with no obvious cause) on his tongue that had emerged since his previous visit several months before. A biopsy by an oral surgeon showed moderate dysplasia -- not cancer -- so an excisional biopsy to remove the whole thing wasn't done for a month. By then it had become very early stage cancer. (Note: Many leukoplakias do not turn all the way to the dark side.)

Perhaps wilckdds or DrMike, both dentists who post here frequently, can offer explanations for what you are seeing.

But if my dentist said something "didn't look good," I'd be on the phone for a second opinion. I see you are in Maryland -- Johns Hopkins is #1 for ENT and #3 for cancer in the latest US News rankings, and has dentists on staff at its head and neck cancer clinic.
All the best,
Leslie


Leslie

April 2006: Husband dx by dentist with leukoplakia on tongue. Oral surgeon's biopsy 4/28/06: Moderate dysplasia; pathology report warned of possible "skip effect." ENT's excisional biopsy (got it all) 5/31/06: SCC in situ/small bit superficially invasive. Early detection saves lives.
#29558 11-06-2007 04:00 PM
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I think the comment "doesn't look good" coupled with the comment "see us again in 3 months" are indicative of one thing for certain.... you need a new dentist. Just think about it - the two comments are incongruous with each other. If it's something that is bad....why not get off your ass and see that the patient gets a referral to someone for a second opinion and biopsy? This is what gets dentists sued, and what gives patients later staging, which means more morbidity and worse outcomes. Freaking amazing. If they don't know what it is, it is their responsibiity to see that you get in the hands of someone who will.


Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.
#29559 11-06-2007 04:51 PM
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Me Personlly hearing Somthing dosent look good ....Means FIX IT NOW..... AND LISTEN TO BRIAN , and everyone else here . I let mine go for 9 months ..I was LUCKY , I can't tell you how lucky , lucky lucky I was .I know that now. Was I lucky to have cancer NO. BUt for what could have been !!!!! My dentist and Dr didn't think somthing was wrong ...you have some one telling you somthing is.. For your self and your peace of mind ...YOU must care ..you are hear asking ....so another dentist and ENT or even That dentist ..CHECK IT NOW!!! fOR YOU !!

Shar


Sharlee
35 year old Female Non smoker, very occasional alcohol ..Scc T1N0M0,partial glossectomy and left neck disection ,2/9/07 No rad deemed ness. 4/16 tonsillectomy ..Trimengenial Neuralga due to surgery
#29560 11-07-2007 02:25 AM
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Thank you all for your responses! I am headed to the ENT Friday! I will keep you posted. Good luck to all my prayers are with you.

#29561 11-07-2007 05:02 PM
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Kershaw,

It's good that you are going to the ENT this week. Brian is right as always, you need a new dentist. General rule is that if something hangs around for 2 weeks, it should be biopsied.

Please keep us posted about what you find out.

Jerry


Jerry

Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.

"Whatever doesn't kill me, makes me stronger"
#29562 11-08-2007 02:30 AM
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What is the differnce between going to oral surgeon or an ENT? Which one would you recommond?

#29563 11-08-2007 04:53 AM
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Dear K,

I have found that there is a good bit of overlap in services performed by oral surgeons and ENT's....and even, in some cases, plastic surgeons.

Which one is best depends on their training and experience. For example, our local oral surgeon is a dental professional, doing great work with difficult extractions and even some bone grafting. This particular man, in this small city, does not have the patient volume to give him the experience to deal with major cancer surgery. He did my biopsy, but he would not consider....nor would I have considered him.....for my surgery.

The same goes for the ENT's here. They might be helpful in diagnosing cancer and referring a patient to the larger centers, but they are not experienced enough to do the surgery and follow-up treatment.

I was referred to an Oral and Maxillofacial surgeon at our state medical school. He has both a DDS and an MD degree. He is well known nationwide, and he did a great job on my surgery, doing all of my extensive surgery without making an incision on the outside of my face (exc. for the neck dissection, of course.)

I had wanted to go to M.D.Anderson.....and will if I have any recurrence....but we had a snafu in communication. As it turns out, the doctors who do this work at MDA are ENT's, and they usually do a facial incision for surgery like mine, so I escaped that, just by chance.

I don't doubt that I received the very best surgery possible. And I feel that my surgeon was well-versed in follow-up care. I, fortunately, did not require radiation or chemo, according to national treatment guidelines, but it made me nervous not to have gone to a large cancer center with a team approach. This anxiety alone made me uncomfortable and pointed out the importance of having confidence in your treatment team.

Six months after my surgery, I went to MDA for some second opinions, to be certain that I had been treated in the most proper manner, and they agreed that I had been treated just as they would have.

My discomfort with not having gone to the large center taught me the value of having total confidence in one's treatment. That is a very important factor.

So.....once you get a diagnosis through your local ENT, my advice is to go then to a large center where they treat head and neck cancer all the time, and let them decide which specialty is best for your treatment.

I would NOT, personally, (and I am married to a physician) consent to being treated for oral cancer locally. In my opinion, there are not enough patients in a private practice to give a physician the experience he/she needs to treat this properly and thoroughly. You need the advantage of lots of experience, and the team approach. You want the advantage of having a physician who has the experience with tissue preservation, since any removal in the mouth involves tissue vital for oral function.

Sooooooo You asked for an opinion......I just couldn't resist giving you my full answer, since there is no one answer to which is more appropriate, the oral surgeon or the ENT. Your local ENT can biopsy and assist with the diagnosis, but you should then take your results to the CCC of your choice and let them take it from there. They will want to re-test your biopsy most likely. This is a comfort also, to be certain that you are on the right track.

Please let us know what the ENT says tomorrow. Good Luck!


Colleen--T-2N0M0 SCC dx'd 12/28/05...Hemi-maxillectomy, partial palatectomy, neck dissection 1/4/06....clear margins, neg. nodes....no radiation, no chemo....Cancer-free at 4 years!
#29564 11-08-2007 05:15 AM
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I would not presume to make any recommendations about whom you should see; I can only tell you our experience.

An oral surgeon is a dentist with advanced surgical training in the oral cavity; an ENT is a physician with advanced training, including surgery, in treating the area generally known as "ear, nose and throat" (and also includes the mouth).

I expect my husband was initially referred to an oral surgeon because it was his dentist who first identified the area of concern. She was more plugged in to the dental community, and a large part of this particular oral surgeon's practice deals with the identification of oral pathology. (Many oral surgeons primarily do such procedures as wisdom teeth extraction -- that's not whom you would want to see.)

The oral surgeon does not treat oral cancer. When my husband's first pathology report came back, showing moderate dysplasia (not cancer), the oral surgeon referred him to a local ENT to remove the leukoplakia (the oral surgeon's biopsy was on only a tiny part of it). Once the second pathology report, from the excisional biopsy, came back as showing SCC, my husband switched his care to an ENT cancer specialist at Johns Hopkins, about an hour away. The ENT in northern Virginia is very good, but he also deals with sleep apnea, hearing loss and such.

Because my husband's cancer was totally removed in the excisional biopsy, he is seen through the regular Hopkins ENT department, not at the Kimmel Cancer Center, but his doctor is one of the oral cancer specialists.

Hope this helps. Let us know how your appointment goes tomorrow. (And I agree completely with Colleen about getting your care, if you need it, at a large cancer center with a dedicated head/neck cancer clinic. That's all they deal with.)

-- Leslie


Leslie

April 2006: Husband dx by dentist with leukoplakia on tongue. Oral surgeon's biopsy 4/28/06: Moderate dysplasia; pathology report warned of possible "skip effect." ENT's excisional biopsy (got it all) 5/31/06: SCC in situ/small bit superficially invasive. Early detection saves lives.
#29565 11-08-2007 08:37 PM
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Kershaw,
My 2 cents worth.
First, I have to agree with Brian and Jerry, find a new dentist. I find it very unprofessional and unethical for a dentist (or any other professional) to tell you, "it didn't look good but they would wait and see until my next visit (3 months). " A lot can happen in three months. I really wonder if this guy knows the thought process and worry he kindled in you.
Second, can you see the white spots? Are they on both sides? My suspicion is that they are only on the lower and on both sides.
Third, ENT's and Oral Surgeon's are not all created equal. I would not rule out either specialty as long as you are certain they have the knowledge and skills and experience to treat you.
I know some are going to disagree with me here, but read the whole post before you get your back up.
The scope of practice of ENT's, Oral Surgeons and many other specialities for that matter depends upon the interests of the individual. I personally know ENT's who have not been in an O.R. since specialty school, I also work and refer to an ENT who is on the local Tumor Board, he was a dentist for five years and went back to school and now is a Surgical ENT and MO who limits his pratice to the treatment of OC and H&N cancer. On the other hand, I know Oral surgeons who basically do limited surgery and take out wisom teeth. I also have an Oral surgeon who I refer to who was in dental school when I was there. He finished his training and then went to Italy for two years to study Oral Cancer Treatment and Facial reconstruction. He is a Dentist, Medical Doctor, Board Certified Oral Surgeon, and holds Diplomas in Oral Caner treatment and Facial reconstruction. I'm wandering here...
My point is ...check the credentials of your doctors, ask them about their experience in treating similar patients.
I believe that a team approach in a major cancer treatment center is the best avenue for any cancer treatment. I only mention the above regarding individual specialists for thos who cannot go to a CCC. So check the credentials.

E-mial me if I can answer any questions or help you in any way.

Cheers,

Mike


Dentist since 1995, 12 year Cancer Survivor, Father, Husband, Thankful to so many who supported me on my journey so far, and more than happy to comfort a friend.
Live, Laugh, Love & Learn.
#29566 11-09-2007 02:13 AM
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Thanks Mike. What my dentist said is that where my wisdom teeth were taken out it shows a white patch that does not come off on my left side of the mouth. I also have a very dry mouth. I am headed to the dtr. today and will see what happens. Thanks so much to all for you support and knowledge.

#29567 11-20-2007 11:22 AM
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I had my biospy today. Boy that was quite a lot of skin they took. I now have to wait 7-10 days. I am not sure what to think. Do you think I need to be concerned since they went ahead and did a biospy??

#29568 11-20-2007 11:23 AM
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Sorry I spelled biopsy incorrect.

#29569 11-20-2007 02:41 PM
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Hi,

I would be concerned if they DIDN'T do a biopsy. This is the only way you will know if anything is wrong. With the holiday this week, the biopsy results will take longer than usual. I would still call the office in a week to see if it came back. My experience is that biopsy results don't usually take more than 3 working days.

And don't worry about the spelling. If korect spelng wuz a reqirament too posst hear, nun of us wood bee alowed on the fourum.

Jerry

Sorry...as my kids would say, "too corny, dad"


Jerry

Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.

"Whatever doesn't kill me, makes me stronger"
#29570 11-26-2007 03:26 AM
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Very nervous! Results are in waiting to hear from the doctor. Will keep you posted.

#29571 11-26-2007 04:13 AM
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we are here waiting with you !


Sharlee
35 year old Female Non smoker, very occasional alcohol ..Scc T1N0M0,partial glossectomy and left neck disection ,2/9/07 No rad deemed ness. 4/16 tonsillectomy ..Trimengenial Neuralga due to surgery
#29572 11-26-2007 09:48 AM
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good luck with Biopsy and prayers are with you.

Whatever you do in a process like this, do not wait and seek treatment and as much advise as soon as possible. Time is an enemy. The inidividuals on this website seem to give good advise and wish I had found this prior to my treatment. I heard prior to treatment (I had neck lymph involvement - advanced diease) words like neck dissection, radiation, chemo (cisplatin, carboplatin and others), Erbitux, neoadjunctive treatment with chemo, imune response treatment between surgery and treatment, three drug chemo, etc. Knowing where to go and making a decision is key. As Brian said your dentist should have sent you someplace sooner. Hopeful it is only nothing and you can move on without issue.

best

Michael J.

Stager IV T1N2bMO base tongue dx 7/6/06 tx 9/22/06


michael J.
#29573 11-27-2007 03:28 AM
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Ok I received my biospy results but have yet to see the doctor. Can anyone help me with this. It read Lesion of Left Retromolar Area: Portion of Squamous Mucosa with Hyperkeratosis? Thanks

#29574 11-27-2007 09:20 AM
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Hyperkeratosis is a thickening of the outer layer of the skin, which contains a tough, protective protein called keratin. This thickening is often part of the skin's normal protection against rubbing, pressure and other forms of local irritation, and causes calluses and corns on hands and feet or whitish areas inside the mouth. Other forms of hyperkeratosis can occur as part of the skin's defense against chronic (long-lasting) inflammation, infection, the radiation of sunlight or irritating chemicals.


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
#29575 11-27-2007 12:08 PM
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Kershaw,
Hyperkeratosis is exactly as Cookey described it.
It can grow and become larger but usually only in response to a local irritant, trauma, and or chemical.
Actinic Keratosis can be a premalignant condition, but generally hyperkeratosis is a benign condition that will go away when the causitive agent is eliminated.

Hope this is of some use to you.

Mike


Dentist since 1995, 12 year Cancer Survivor, Father, Husband, Thankful to so many who supported me on my journey so far, and more than happy to comfort a friend.
Live, Laugh, Love & Learn.
#29576 11-28-2007 04:27 AM
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Thank you both for your help. So this condition is not cancer?

This site has been wonderful and I wish everyone the best!

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