Previous Thread
Next Thread
Print Thread
Page 1 of 2 1 2
#125570 12-02-2010 09:50 AM
Joined: Dec 2010
Posts: 3
Member
OP Offline
Member

Joined: Dec 2010
Posts: 3
Hello,
I am new to ocf. Yesterday I received biopsy results from lesion excised from my tongue. The report indicated squamous cell carcinoma, well differentiated, superficially invasive. I was referred to a doctor at the greenebaum cancer center at the university of maryland. They reviewed the report and indicated that another biopsy would not be required. I have an appointment at the center next week.

Can anyone tell me what to expect next?



69 yr, dx 11/18/10 SSC well differentiated, superficially invasive. stage/treatment to be determined
Joined: Apr 2009
Posts: 329
Platinum Member (300+ posts)
Offline
Platinum Member (300+ posts)

Joined: Apr 2009
Posts: 329
Hi James,

About all I can tell you is what Moffitt Cancer Center did to me, tongue cancer. I had my biopsy, went to Moffitt Cancer Center in Tampa to see the surgeon. My lesion was growing outward, but it had grown under my tongue, 2cm. My surgeon explained to me he would take the tumor out and do a ND cut from my ear to the middle of my throat. When he told me that my eyes got huge. The CT Scan showed no nodes invloved, my surgeon told me CT scans do not pick up small cells. He suggested I have a ND to be on the safe side but it was up to me. I told him do what you have to do, he did it. You can't see my scar because of my age he made the cut in a wrinkle. I guess aging is good in some ways.

I was in the hospital 2 days, I wanted out so I did everything I was told to do before I could leave. I was on Roxycodyne for 2 weeks then went to tylenol. As far as scar tissue in my tongue and neck it acts up once in a while. I ususally massage the area and the stiffness goes away. I can feel a little knot in my tongue, no big thing. I do have a small speech impediment, when I talk fast it seems to get worse. After surgery your case goes before the tumor board to see if you need Radiation/Chemo in my case I didn't need it.

Your case may be different, sharing what was done to me. It sounds worse than what it was.

See my signature line. It's a good idea to make one it's under My Stuff at the top.

I hope all works out for you do what the surgeon suggests you'll be fine. Good Luck keep us posted.

Connie


SCC. of the left lateral tongue, anterior two thirds, T1 possibly a T2.
Left partial glossectomy, left selective neck dissection 4/21/09. Nodes clean, No Rad, No Chemo.

CT Scan 9/11 clean, CT Scan 9/12 clean


Moffitt Cancer Center in Tampa, FL. A+.

My hometown Lockport, NY.



ConnieFL #125578 12-02-2010 01:05 PM
Joined: Sep 2006
Posts: 8,311
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)
Offline
Senior Patient Advocate
Patient Advocate (old timer, 2000 posts)

Joined: Sep 2006
Posts: 8,311
James,

Depending upon the size of the tumor and whether or not there is nodal involvement, your treatment can include anything from removal of the Primary, neck dissection(s), radiation and chemo. Can be Primary surgery alone or all of the above. No one here can tell you what's in store for you at this point. You will have to wait and see what they recommend and even then you may want to get another opinion.

Tell us what they say and then we can tell you everything (and more) about what you may expect.


David

Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
ConnieFL #125584 12-02-2010 02:39 PM
Joined: Dec 2010
Posts: 3
Member
OP Offline
Member

Joined: Dec 2010
Posts: 3
Hi Connie,

Thank you for your response. At this point any info I can get is helpful in getting my head around this problem.

Many thanks. Hope to talk to you again.

jim


69 yr, dx 11/18/10 SSC well differentiated, superficially invasive. stage/treatment to be determined
davidcpa #125585 12-02-2010 02:40 PM
Joined: Dec 2010
Posts: 3
Member
OP Offline
Member

Joined: Dec 2010
Posts: 3
Hi David,

Thank you for your response. At this point any info I can get is helpful in getting my head around this problem.

Many thanks. Hope to talk to you again.

jim


69 yr, dx 11/18/10 SSC well differentiated, superficially invasive. stage/treatment to be determined
Joined: Jun 2007
Posts: 5,260
Patient Advocate (old timer, 2000 posts)
Offline
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 5,260
James, My wish for you is that you don't need all of the surgeries a lot of us had , and that you don't have to lose anybody parts. There are a few of us that have had everything but the bathroom sink installed in our bodies. Just as many taken away too. LOL


Since posting this. UPMC, Pittsburgh, Oct 2011 until Jan. I averaged about 2 to 3 surgeries a week there. w Can't have jaw made as bone is deteroriating steaily that is left in jaw. Mersa is to blame. Feeding tube . Had trach for 4mos. Got it out April.
--- Passed away 5/14/14, will be greatly missed by everyone here
EzJim #125627 12-03-2010 05:22 AM
Joined: May 2009
Posts: 1,412
Patient Advocate (1000+ posts)
Offline
Patient Advocate (1000+ posts)

Joined: May 2009
Posts: 1,412
James,
You came to the right place. I to had a lesion on my tongue that came back as SCC. I, however, did not get a ND. I did have radiation and chemo. Your physician may decide not to do radiation at this point if he/she gets clear margins. May wait until after a PET scan to determine what needs to be done.


Angelia
31 at Dx.
DX: 4/30/09, 10/21/09 SCC on floor of mouth,
T1NOMO, T2N1M0
TX: 39 IMRT, 8 cisplatin 11/30/09
PET/CT: 11/03/09: Lymph node involvement
PEG/PORT: 11/09
TX end: 02/01/10
PET Scan: 04/05/10 clear
PEG Out: 06/21/10
Biopsy: 12/23/10: fibrosis
HBO: 01/04/11 - ORN
Baby girl born 11-30-12
walknlite #125646 12-03-2010 03:57 PM
Joined: Jun 2007
Posts: 10,507
Likes: 7
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)
Offline
Administrator, Director of Patient Support Services
Patient Advocate (old timer, 2000 posts)

Joined: Jun 2007
Posts: 10,507
Likes: 7
James, welcome to OCF. Here is a list of the best cancer centers. Its a good idea to make sure you are being treated at a facility that is familiar with treating alot of oral cnacer patients. A second opinion is also a very good idea.

http://health.usnews.com/health/best-hospitals/cancer-hospital-rankings/


Christine
SCC 6/15/07 L chk & by L molar both Stag I, age44
2x cispltn-35 IMRT end 9/27/07
-65 lbs in 2 mo, no caregvr
Clear PET 1/08
4/4/08 recur L chk Stag I
surg 4/16/08 clr marg
215 HBO dives
3/09 teeth out, trismus
7/2/09 recur, Stg IV
8/24/09 trach, ND, mandiblctmy
3wks medicly inducd coma
2 mo xtended hospital stay, ICU & burn unit
PICC line IV antibx 8 mo
10/4/10, 2/14/11 reconst surg
OC 3x in 3 years
very happy to be alive smile
ChristineB #125656 12-03-2010 07:17 PM
Joined: Sep 2009
Posts: 618
"Above & Beyond" Member (500+ posts)
Offline
"Above & Beyond" Member (500+ posts)

Joined: Sep 2009
Posts: 618
James,

I think the key words you received are �Superficially Invasive�, this is a good thing. My cancer was �minimally invasive� meaning mine was just a bit more invasive then yours. Let�s hope this holds up as they do further tests. I was treated with radiation only with no chemo and no neck dissection because they caught it early.

I hope you are as lucky as I was. I�m cancer free (knock on wood) 1 year out and back at living life 110%. Treatment was an unmitigated BITCH and I was laid very low for some months, but I�m on the other side of that now and back in the game.

Make sure you get an opinion from a CCC. I got two although I was treated at a nearby cancer center that used the same protocol as the University of Michigan (my closest CCC).

Good Luck and keep posting.


Kelly
Male
48, SCC (Soft Palet) Rt.,
Stage 1, T3n0m0,
Dx, 8-09, Start IMRT 35 9-2-09 end 10-21-09
04-20-10 NED
8-11 recurrence, node rt. neck N2b
10-11 33 IMRT w/chemo wkly
3-12-12 PET - residual cancer
4-12 5 treatments with Cyberknife & Erbitux
6-19-12 Pet scan CLEAR
12-3-12 PET - CLEAR
Kelly211 #125661 12-04-2010 12:39 AM
Joined: Oct 2006
Posts: 383
Platinum Member (300+ posts)
Offline
Platinum Member (300+ posts)

Joined: Oct 2006
Posts: 383
James:
Expect the unexpected. Listen to what the doctors have to say, make notes, then research. Share with the folks here and to David's point a second opinion is usually a good thing. I was actually encouraged by the first surgeon I spoke with to get a second opinion, but as he said, Don't waste too much time as it is of the essence that you take action. Cancer never sleeps. Sounds as though it is discovered early so you will still fight but will win!
Steve


SCC right side BOT/FOM; DX 1-25-06; Neck dissection/25% of tongue removed 2-17-06. Stage 2 Recurrence 7-06: IMRTX35 & 3X Cisplatin ended 10-18-06. Tumor found 03/18/13; Partial Glossectomy 03/28/13 left lateral tongue. Nov. 2014; headaches,lump on left side of throat. Radical Neck Dissection 12-17-14; Tumor into nerves/jugular; Surgery successful, IMRTX30 & 7X Erbotux. Scan 06-03-15; NED! 06-02-16; Mets to left Humerus bone and lesion on lungs-here We go again! Never, Ever Give Up!

**** PASSED AWAY 10/8/16 ****

Page 1 of 2 1 2

Link Copied to Clipboard
Top Posters
ChristineB 10,507
davidcpa 8,311
Cheryld 5,260
EzJim 5,260
Brian Hill 4,912
Newest Members
amndcllns01, Jina, VintageMel, rahul320, Sean916
13,104 Registered Users
Forum Statistics
Forums23
Topics18,168
Posts196,927
Members13,104
Most Online458
Jan 16th, 2020
OCF Awards

Great Nonprofit OCF 2023 Charity Navigator OCF Guidestar Charity OCF

Powered by UBB.threads™ PHP Forum Software 7.7.5