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"OCF Canuck"
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"OCF Canuck"
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Hello, three weeks sounds long to wait for a biopsy, here in New Brunswick, Canada it takes a week to just a bit over a week and NB is one of the slower provinces. My husband had to get a biopsy after his surgery and prior to his radiation to insure he did not have a reacurance and it took one week. The pathology report after the surgery took almost a month, usually it takes three weeks. (In this case they are studying the entire surgical resection slice by slice)

Know that you are doing everything you can, Sophie


husband 61@diagnosis painter
6/9/13 Exophylic invasive SCC IV(ext.gingivobuccal) 3cm+ mandibular/lytic/erosion, jugular/node9mmshort-axis
17/9/13 Dx(moderately aggressive)
24/10/13 left madiblectomy, mod radical neck disct, leg flap, NGtube
2/01/14 (30 tx)rads 60gy
N2b (2nodes under jaw) (rem. in tiny nerves) (rem. 30 nodes)
Clear margin, close 2mm inner cheek
15/05/14 cellulitis
3/12/14 Chest CT Clear
27/02/15 cellulitis
8/6/15 cellulitis
10/6/15 Osteomyelitis
Joined: Oct 2014
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"OCF Canuck"
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Thanks Sophie!

After reading your post I thought enough time had pass for at least a follow up call as it would be 2 weeks I've wait for the biopsy results this Wednesday.

They said the results are not in yet. I did express my concern and worries to the receptionist. The receptionist just said, to be honest if the lab found anything alarming with the biopsy they would have call almost immediately to let us know to make an appointment with the patient, so just try to relax and wait for your scheduled appointment. She also said she's just talking from her experience so don't take what she says as the end result but just try to relax for now.

So I guess this has calmed me down for now.

P.S - I also would like to apologize to you all for my last post. I guess that was too revealing to everyone and I was having a panic attack. I'd just like to be as transparent as possible to anyone who might be in the same situation as me.

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"OCF Canuck"
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Hey everyone. Results from the biopsy came back, it's just a cyst.
The official wording of the biopsy was this:

[quote]Gross Description: The specimen consisted of one piece of tan soft tissue, measuring 0.5x0.5.0.3cm. It was bisected and submitted in total for histology

Microscopic Description: Sections show oral mucosa composed of stratified squamous epithelium overly fibrous connective tissue. There is an invagination of surface epithelium into the underlying connective tissue that is partially lined by parakeratinized stratified squamous epithelium, containing some desquamated keratin and surrounded by a wall of lymphoid tissue with germinal centers.

Diagnosis: Tissue from right posterior tongue base: consistent with lymphoepithelial cyst.[/quote]

Sorry about saying "dime sized" in my initial post, guess it was smaller. Hope it's not a bad thing that I posted my full results but I just wanted my situation to be transparent as I said before.

So what's next for me? I'm just going to try to relax for now. I have a follow up appointment in 6 months with the Oral Maxillofacial Surgeon just to see if it grows back.

I also (basically begged) my doctor for a referral to see the best ENT specialist in my city to have a better look at my throat as I can see what appears to be bumps, or papillomas at the back of my throat. My family doctor said it's just cobblestoning of the throat and I shouldn't be worried, but I insisted on the referral. The line is long and I probably won't see this ENT until around May next year as my case is considered low priority with this diagnosis.

Thanks for all your help everyone. If this was stressful to me for the past month and a half I can't imagine what it was like for you all... you all are truly soldiers.

I'll still be poking around these forums every now and then. As always appreciated, let me know what you all think.

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"OCF Canuck"
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"OCF Canuck"
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That's terrific - see now you know!


Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
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Thanks Cheryl!

I just wish the Greater Toronto Area had some sort of screening to test for pre-malignant/dysplasia in oral tissue.

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"OCF Canuck"
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You need to find a top notch ENT to keep an eye on you. smile


Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
Joined: Sep 2013
Posts: 105
"OCF Canuck"
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"OCF Canuck"
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I second Cheryl, when you have had oral growths or irregularities you need to have follow ups with an ENT specialist and do a regular check up on yourself for any changes.
All the best and I am so happy to hear the good news, Sophie



husband 61@diagnosis painter
6/9/13 Exophylic invasive SCC IV(ext.gingivobuccal) 3cm+ mandibular/lytic/erosion, jugular/node9mmshort-axis
17/9/13 Dx(moderately aggressive)
24/10/13 left madiblectomy, mod radical neck disct, leg flap, NGtube
2/01/14 (30 tx)rads 60gy
N2b (2nodes under jaw) (rem. in tiny nerves) (rem. 30 nodes)
Clear margin, close 2mm inner cheek
15/05/14 cellulitis
3/12/14 Chest CT Clear
27/02/15 cellulitis
8/6/15 cellulitis
10/6/15 Osteomyelitis
Joined: Oct 2014
Posts: 12
"OCF Canuck"
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"OCF Canuck"
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Joined: Oct 2014
Posts: 12
Thanks for the advice Cheryld and Sophie! They actually moved up my ENT appointment, it's not the ENT I wanted to see unfortunately but its at Credit Valley Hospital in Mississauga (near Toronto). So I'll see how that goes on Thursday this week.

Joined: Sep 2013
Posts: 105
"OCF Canuck"
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"OCF Canuck"
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Cheers, relieved for you! Sophie

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