CSN Login
Members Online: 5

You are here

An incidental finding=RCC

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

I just found out that I have RCC.  I originally hurt my lower back by lifting a heavy object.  I began to experience pain in my abdomen, mainly left side of abdomen to the rib cage. Although the pain was along the left side the CT scan did not show muscle tear or any anomoly in that area but a 7cm size tumor at my right kidney. These type of situations are called "incidental finding"...funny....Im calling it a blessing in disguise.  

My Urologist recommends radical nephrectomy. Im still processing the information and also trying to keep a positive mind set but do have to admit feeling very scared.  I have two small children and an amazing husband.  I cant fanthom the idea of this disease taking a turn and wreaking havoc.  I have only had one formal Dr. visit, the day i got the diagnosis, and he seemed very optimistic and certain that it is contained in the kidney only.  My chest x-ray looks clear.  Although this diagnostic image is promising cant help but wonder if any microscopic cancerous cells are floating around about to take up residence elsewhere.  This is the first time in the last 2 weeks that I vocalize this worry.  I figured this would be an appropriate forum to do so.  I am trying to be positive and optimistic around my family for their sake and for mine as well but negative nancy tends to rear her head from time to time. Embarassed

I look forward to reading other members experiences.  Im scheduled for kidney removal until 5/9/17.  No earlier dates available. Ive learned a lot about "staging" and now can ask more pertinent questions when I meet with my doctor again.

Is RCC considered in situ when its size warrants a radical nephrectomy?

Major lifestyle changes knocking at my door.  Have to ease the stress on my soon to be solo-kidney!

 

 

 

 

icemantoo's picture
icemantoo
Posts: 3354
Joined: Jan 2010

bee,

At 7cm a radical nepherectomy is almost a given. Seven cm is also the division between Stage 1 and Stage 2. The exact size and pathology will not be determined until after surgery. There are members here with larger tumors who have had no problems since surgery and they will chime in. Mine was a little larger than 4 cm and so far so good with almost 15 years behind me. The surgery is not fun, but you should have it easier than me as you are a bit younger. The only uncertain part of your surgery will be whether it is laproscopic or open and there are a lot of factors that go into that decision such as location of the tumor. Sometimes they start with a lap and make a game time decision to go open. Get some help lined up  to handle the young ones for the first few weeks after surgery. We all went thru the not so fun time when we were told we had Kidney Cancer and the first thing we were told is that they want to yank out your kidney. That feeling will subside over time. It took me almost 11 months after surgery to get back up on water skis. No roller coasters this simmer.

 

 

Icemantoo

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Hello icemantoo!!!

Thank you for wonderful feedback.  I am very happy that you have had such a promising prognosis and back on water skis? good for you! Hopefully roller coasters soon! Thanks for the suggestion of lining up help with my boys.....I may be underestimating the healing and recovery time...I better prepare and have all my bases covered!

 

Steve.Adam's picture
Steve.Adam
Posts: 463
Joined: Oct 2016

You picked the perfect forum to talk about nephrectomies. Everyone here has a special interest.

If you browse through the message topics for the past few weeks or months you will find lots of questions and answers, many of which will be relevant to you.

My radical right nephrectomy was on February 6th. I'll be having some blood tests in a week and then I'll be able to tell you my kidney function 8 weeks out.

Anyway... Welcome to you and Nancy too.

Steve.

 

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Hello there Steve,

Yes, I have already learned a lot just from reading many posts and I feel very conforted arminng myself with knowledge and peoples personal experiences.  So do you feel like your back to your usual or still recovering physically? How often do you have to go for follow up exams? I hope you have good results at your next blood evaluation!

Thanks for taking the time to welcome me to the group.  I hope to offer relevant information once I get through my phase of treatment!

Cheers!

Bee

Steve.Adam's picture
Steve.Adam
Posts: 463
Joined: Oct 2016

Yes, I feel pretty much back to normal. I am still being careful about lifting etc., but everything else is fine. My energy levels are ok. No pain, no discomfort. I do feel something a little different inside when I take a deep breath.

I haven't yet had any follow up visits to the Urologists, just to my local doc to get my staples out.

Now that it is all done I feel like a character in a story that I just finished reading.

Actually I felt a bit like that before the surgery. I was the star of my own (medical) reality show.

That feeling probably helped me to put some distance between me and the events I was living/acting/watching.

What will the next chapter bring? 

Steve.

 

 

Bay Area Guy's picture
Bay Area Guy
Posts: 519
Joined: Jun 2016

I have to admire your attitude about this, calling it a blessing, but, you are absolutely right.  Your tumor was discovered at a time when it can still be treated relatively easy and you should have no problems going forward.

I'm nine months out from having a baby lesion (1.8cm) taken out in a robotic assisted partial, so my surgical experience isn't really pertinent to your situation.  But I do recall my initial attitude when finding out about the diagnosis was no where near as good as yours.  Had I had hair, I would have been running around pulling it out in the first few hours.  Fortunately for me, my sister is a nurse practitioner (in a different field), so she was able to explain a lot of things to me and calm me way down.

Best wishes for an uneventful surgery and a full recovery.

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Hey there Bay area guy...Im from the Bay area too! and although I may not be pullig my hair out I sure have thinned out my eyebrows..thats my nervous tick...I get stressed and there I go plucking away  without realizing it....lol...Well I dont think this Cancer situation is a blessing because its such a nasty, terrible, weird body glitch....but me hurting my back at work was the blessing which led to the discovery of cancer.  Apparently by the time people find out its much more evolved.  How did you find out you had kidney cancer? I wish you continued good health and look forward to your response!

P. S. Looks like a small part of the Bay Bridge left...Just noticed today as I went in the visit family.

Cheers,

Bee

Bay Area Guy's picture
Bay Area Guy
Posts: 519
Joined: Jun 2016

Hi Bee.  I found mine out by accident.  I get a physical every year and as part of the physical, blood and urine tests are done.  My urine test came back positive for microscopic amounts of blood.  So, my doc, figuring it was likely a kidney stone, sent me in for a CT scan.  Surprise!  The report came back as a small lesion on my right kidney.  That was in December, 2013.  The urologist I got referred to at Stanford recommended a wait and see approach, having me get scans (alternating between ultrasound and CT) every six months.  It wasn't until April, 2016 that an US detected that the little bugger had grown from about 1.5cm to 1.7cm, so he had me go in for a robotic-assisted partial, also at Stanford, on June 22nd.  I checked in at noon; the operation started at 3PM; the fire alarm apparently went off around 4PM; I was back in a regular room at 7PM; and I was released at 1:30PM the next day.  The pathology showed chromophobe RCC, a very slow-growing form of RCC which rarely recurs and rarely spreads, so I have counted my blessings.  My six month scan/chest xray in January showed all clear, so we'll do it again in July and if that's clean, he'll have me go every 12 months for a while, which is fine by me.

The funny thing about the blood in my urine is that was the one, single time it ever showed up.  At my physicals in 2014 and 2015, there was no trace of blood.  If not for that single occurrence, I wouldn't know I had the lesion.

Skagway Jack's picture
Skagway Jack
Posts: 224
Joined: Oct 2013

Bee,  Mine was 7x5 cm and after removal they referred to it as baseball sized lol.  They catagorized me as stage 1B.  So far NED now since removal in October 2013.   Good luck! You will like the folks here though I am sure there are other places you would like to be. 

Jack C

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Wow! Sounds like mine may be a baseball sized one too! Did you experience pain prior to removal of it? I am comforted in knowing that you are doing well since your treatment.  That is awesome! 

I strongly believe that every situation or curve ball we are dealt with is an opportunity to learn and grow from.  I can assure you that I can hear every bird chirp around me and I can smell every dog gone flower around me.....suddenly the little things seem to be more relevant now.  Im grateful for the people here and their openess and honesty about their struggle and process! 

cheers!

-Bee

Skagway Jack's picture
Skagway Jack
Posts: 224
Joined: Oct 2013

Bee

In my case I had gross hematuria (blood in the urine).  If I hadnt been using the restroom inside and looking at the result I would have never known as I felt nothing out of the normal.   I had been loosing some weight leading up to it, but no pain that warned me.  I definately agree with the stopping to smell the roses and living and loving more deeply. 

 

Jack

BoondockSaint's picture
BoondockSaint
Posts: 242
Joined: Mar 2017

Hi Bee. Please read my post from a few weeks back. My wife's tumor was found in a similar fashion. Today is 19 days post surgery and she is doing great. incision scars are healing well. She feels probably back to about 80%. Fatigue is her big nemesis right now but that's even getting better. She has a stray random pain from time to time and a little pain in her kidney area of her back but it usually subsides quickly.

we had a great weekend and got out and enjoyed the nice spring weather. You're gonna do well. This is a great place. 

Big hugs.

Boondock out!!

stub1969's picture
stub1969
Posts: 923
Joined: Jul 2016

I'm glad you found this site.  I've said it before and I'm sure I'll say it many times in the future....this site is a wonderful place.  The members will reach out and support you and offer their stories and experiences to help.  I'm just over 6 months post-surgery and doing well.  I've been back to running and exercising without issues at 3 months post-surgery. 

Can I ask where you are being treated?  Do you know if your doctor specializes in RCC?  I ask because it seems odd that surgery is out over a month for you.  As Iceman said 7cm is the right on the line of a stage 1 and 2.  Surgery for me was a couple weeks after I met with the urologist.  My intent is not to add to your anxiety, I'm just curious.

Take care,

Stub

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Wow back to running already? that is amazing and inspiring!  I will be treated at my local Kaiser Permanente hospital in Walnut Creek, CA.  The Urologist that gave me the diagnosis is the Dr. who will also be doing the surgery but Im not sure if he specializes in RCC.  Im glad you asked.  Im sure it makes a difference right? Oh my....my list of questions for him is growing exponentially...lol...another great reason for joining this forum...to learn and get insight from ya'lls experience.  His nurse/assistant indicated that he was booked until May and that they were going to try to move some patients around to accomodate an earlier surgery date for me but I guess it didnt work out that way.  Draw backs of having an HMO plan I guess.  

I'm glad that you are doing well and wish you continued good health!

-Bee

 

marosa's picture
marosa
Posts: 333
Joined: Feb 2015

You have such a positive attitude!  That is fantastic and it will carry you a long way, hang in there, you will be fine!  I too had a pretty long wait, a little over 5 weeks from the time of diagnosis.  My tumor was almost the size of yours but I, like Steve, had an artery leak hours after the surgery. In my case it went with the  risk of going with a partial at that tumor size.  

It looks like you will pass thru this with flying colors!  Keep up your positive attitude and your spark for life!  It will do wonders for you and we will definitely profit from it too!  May this few weeks go by fast for you.

Steve.Adam's picture
Steve.Adam
Posts: 463
Joined: Oct 2016

I should have read your 'my csn' page earlier. I thought I was the only one here who'd had that problem.

Mine was also T1b Grade 2 and my hospital stay was also 9 days.

I had a very easy recovery and I have wondered if the long stay in hospital helped.

Steve.

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Thanks for sharing your story.  Im sorry you had a slight complication. How was that? did you feel like something was wrong? that is very scary.  Im glad your well now.  My step mother passed away three years ago from many complications of breast cancer.  It was her second round in a 15 year period.  She unfortunately became negative, mad, resentful, toxic.  It was very sad to see her go through such a change in her character and I strongly believe it added to her loosing her fight to stay alive.  I think that if I stay positive and grateful for what I have and experience that good things/experiences will come as a result.

May the next couple of weeks be a blurrrrrrr!!! :-)

Steve.Adam's picture
Steve.Adam
Posts: 463
Joined: Oct 2016

I was still unconscious after the surgery when the complication (leaking artery) happened. It seems to be quite rare. Marosa is the only other case I heard of here since I joined in October. There was one other case but I don't remember where I read about it. That was an artery cutting tool that malfunctioned and cut an artery without clamping it. Similar to Marosa's and mine but more serious and also very, very unlikely.

I updated 'My CSN' the other day and told my story briefly there.

I went to the hospital alone. But... When friends/family phoned the hospital to find out how I was they were told that there had been a complication and that I had (or was having) emergency surgery.

So I got more visitors than I would have otherwise, but none brought chocolate... (I don't eat sugar anyway, so no worries.)

Even without the complication I realise that I underestimated the surgery. I was prepared to be tired and to rest for a week or two, but it just turned out to be bigger than I was expecting, even after reading stories here.

Even though I had a fairly easy time really, it was still a shock to my system, emotionally and physically. There is some kind of spiritual effect too, but I'm not sure what that is. Maybe just smelling and seeing the flowers more clearly.

Steve.

pamstayner's picture
pamstayner
Posts: 111
Joined: Apr 2014

Glad you found us.  We are all in the same boat, bailing out the leaks, and rowing the best we can.  

If you have two young kids, who are not at the help out with the wash and dishes or meals... yes, you better get help lined up.  

A radical neph means a good sized incision, lots of inards getting pushed and shoved around to get to the back kidney area.  You will be told not to lift anything heavy... like over 5 lbs.  Be aware, as a mom of two young ones, your purse probably weighs more than 5 lbs... so wake up girl !  It is major surgery.  You will have to take time to let your body get over the shock !  Makes me smile, glad you have an amazing husband.  He better start the transformation now, as a working Mom, you likely believe you are supermom... and this kidney tumor removal will be your kryptoenite.. or however it is spelled.  

Jan 4 you has advice for the tummy swelling and a binder that works wonders.  Use it.  The hardest thing getting used to after the surgery was asking for help.. something I had not ever done before. It was hard.  If your husband will get other family and friends to organize a dinner delivery to your house, and perhaps someone to come in to keep the wash and housework under control, at least for a few weeks after you come home.  Let everyone help who say they want to.... make a list, and have them take a task.  

You will get over the tired fatigue, the soreness, the inability to sleep.  Do not think the "no pain, no gain" montra...  it is stupid in this day and age.

You will be fine. The best thing to do is get well.  Then you will be able to take charge again, and keep your house together.  This cancer is a BIG DEAL.  Your attitude of finding this, and dealing with what may come down the road is good, and will help you tremendously.  Keep a sense of humor, know that the whole lot of us here have your back, and keep us up to date on your progress.

We care.  We are glad you found this site.  Others will chime in I am sure, with good advice .... all from personal experiences.  Good luck

Pam

 

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Thank you! Thank you!

I will round up the troops and ask for help. I am used to juggling and keeping the household afloat but you are right...I better snap out of this denial and be ready to get my innards shook! 

Pain management a must....Im old school but not in the pain department. Wink 

I will keep ya'll posted with my progression as surgery date nears...

cheers!

-Bee

Deanie0916
Posts: 425
Joined: Nov 2016

I am 6 months out from a radical left nephrectomy and I am doing well. I just had my 6 month check up and so far no little offspring of Hubert my evil mass. Mine was 20 cm and partially in the renal vein, so I am very blessed that it hasn't spread more. I love your attitude. Walk as soon as you can and are able after surgery, it will help. God bless you.

JerzyGrrl's picture
JerzyGrrl
Posts: 761
Joined: Jun 2016

Glad you're focusing on being positive. Using your pre-surgery time to be busy, focused, and get organized is great (Although I had quite a few days when I was more that delighted to have simply not made things any worse... Not to mention happy for those times that I hadn't made things too much worse). 

There'll no doubt be occasions when stress and/or tears may decide to show up anyway. Investing in quality tissues is an excellent act of self care for life in general, not to mention before and after surgery time. Oh, and I'm not just talking about YOUR tears and stress. Family and friends will appreciate not sandblasting their noses and eyes with cheap tissues, too (I'm partial to Puffs, doesn't even have to be the kind with lotion). 

Keep us posted - All the best.

Dessert Mom
Posts: 1
Joined: Apr 2017

I went to the ER on 3/24 thinking that I had appendicitis. Wrong! 7 cm mass in the LEFT kidney that it invading the renal vein. Blood work good. Urinalysis good. Chest CT good. It must have been the man upstairs that sent me to the ER.

I am scheduled for surgery  (laproscopically) on the 18th.. next Tuesday. Removing the whole kidney.. I am not versed on all of the official words yet.  I have two children (almost 17 and almost 13) and a husband who is pretty much in denial.. like they are going in to pop a pimple. I have cried buckets of tears.. how I have not dehydrated is beyond me. 

I am trying to freezer cook and make things as simple as possible for post surgery.. but yet make things normal for the kids.

My oncologist says no treatment afterward. What else can I expect?

Steve.Adam's picture
Steve.Adam
Posts: 463
Joined: Oct 2016

I'm sorry this had to happen to you.

They're not wasting any time getting you into surgery (I waited 4 months). That's a good thing but doesn't give you much time to prepare mentally.

You'll get through this and there is a very good chance that you'll be ok in the future.

But that is the future... Right now it sounds like you could use some help at home. You'll be out of action for a while.

We have a few days to get to know you before your surgery. You can start your own message thread on the main kidney cancer forum page.

Steve.

beemurguia's picture
beemurguia
Posts: 57
Joined: Mar 2017

Dessert mom,

Im so sorry to hear of your finding! It sucks doesnt it/?? For some reason RCC really doesnt seem to warrant a whole lot of post operative treatment besides the surgery itself...thats a good thing! I found out early march and im scheduled for surgery 5/9 and im starting to get antsy about having to wait.  My husband although has been always very supportive (cooking, cleaning, homework, laundry etc.etc.) has been non vocal about the "cancer" thing....i can tell he is wound up a little tighter and keeping busy....so i finally sat him down and asked if he had any concerns or questions....he then finally broke down in tears and said he is trying to be strong and doesnt want to show fear so that i not get scared.  Jeez louise...ok...he does care!! 

Crying is good...let it out!!! I wish i could...for some very strange reason I have not shed one darn tear...and i cry when i see a commercial....I have been beyond mellow about this.  I have been extremely sleepy and tired so maybe thats my defense mechanism. Either way I wish you the best possible outcome during and after surgery.  WE are here for you! Please keep us posted!

Ciao!

-bee

stub1969's picture
stub1969
Posts: 923
Joined: Jul 2016

Welcome, Dessert Mom.

I know exactly what you are going through and how you're feeling.  They found my tumor the end of July and a month later I was on the table.  When I found out about the cancer all I could think about was my wife of over 20 years and my children (ages 19, 17 and 10 at diagnosis).  I was really worried about telling them about the mass and surgery.  They handled it much better than I ever expected.  I'm glad you found us.  We'll be able to help as much as you want us to.  I do suggest starting a new thread.  You'll get more responses by doing that. 

You'll get through this,

Stub

foroughsh's picture
foroughsh
Posts: 779
Joined: Oct 2014

Hello

I had a 10 tomur 2.5 years ago and the only treatment I've had so far is radical nephrectomy. Stage one kidneys Cancer's survival rate is very promising with more than 90% rate, although stage two ( larger than 7 cm) is not as promising as stage one, it is still very good with almost 75% and I personally know many stage two patients who are living their normal lives years after their nephrectomy.

I know what you're thinking and how you're feeling since it took me more than a year to come back to almost normal me, some therapy sessions that I had , had to have been the main couse, reaching out to other people with same experience on this board and sharing my emotions with my hubby are two effective and helpful decisions that i've made. I've seen many member who have been very terrified once they were told about their cancer but it took much shorter time for them to overcome their fears and come back to normal life.

Forough

DAC677's picture
DAC677
Posts: 60
Joined: Feb 2017

I think an incidental finding like that is a blessing with this type of cancer.

My story was much the same as yours and after a series of incidents that ended in a golf swing that felt like something tore i knew there was a problem but suspected a hernia. Three weeks later when it didnt heal i saw my pcp and had a cat scan and found an almost 11CM tumor. She told me that RCC often gets discovered so late because it doesnt normally give signs until you are urinating blood. Its also a very treatable type of cancer and keep positive thoughts!

Subscribe to Comments for "An incidental finding=RCC"