Skip to content
Forum IndexForum: Just Diagnosed → Topic: HELP! 10 year old with bc
« Forum: Just Diagnosed: Discuss next steps, options, and resources.

Topic: HELP! 10 year old with bc

Log in to post a reply
  • Posted on: Apr 14, 2009 08:03 pm, edited Apr 16, 2009 11:21 AM by cjsocal
Joined: Apr 2009
Posts: 6
cjsocal wrote:

My ten year old daughter was just diagnosed yesterday (confirmed today) with breast cancer. I have been searching for similar cases but have found nothing. My wife and I have no idea what type, stage, etc... We took her in to have a lump removed that was thought to be completely routine, but the surgeon found a solid mass that appeared to be a tumor behind the suspected area. We were assured that it was probably nothing to worry about but a sample would be sent to pathology. Went to a follow up visit 6 days later (yesterday) and the preliminary results were not good. Got a call today to confirm our worst thoughts. Is there anybody that has heard of such a young girl being diagnosed with breast cancer? We are in a holding pattern now and don't know what to do.

***UPDATE*** 

We just got a copy of the pathology report yesterday and I will read the diagnosis word for word. DIAGNOSIS: Infiltrating ductal carcinoma with focal solid papillary growth pattern and secretory feautures, grade II (moderately differentiated). The tumor extends to the inked surgical margins over a broad front. Approximately 2 cm in aggregate dimension portions of benign prepubertal mammary ductal parenchyma. No ductal carcinoma in situ component identified. Changes highly suspicious for large vessel invasion by tumor but no angiolymphatic space permeation by tumor identified. AJCC stage grouping: T2, NX, MX; stage IIA This was also listed in the microscopic description: This material was submitted for breast prognostic studies with the following results: Estrogen receptor negative, progesterone receptor negative, Her2/neu zero (not expressed) and Ki67 rate of 3% in most of the fields examined. Can someone tell me that my 10 year old daughter does not have breast cancer? We have not told her yet, but know we will as she will be seeing an oncologist within the next day or two.

Page 3 of 14 (416 results)

Posts 61 - 90 (416 total)
Shirlann
Joined: Feb 2002
Posts: 7,043
Apr 16, 2009 07:36 pm Shirlann wrote:

Hi, and let me add my heartfelt grief at this diagnosis.  All I would suggest for now is to be SURE it is breast cancer.  It could be Lymphoma.  So I would go to a second opinion location to be positive this is not an error.

Please know we are all praying for your family.

Gentle hugs, Shirlann

Towhee
Seattle, WA
Joined: Jul 2007
Posts: 651
Apr 16, 2009 11:17 pm Towhee wrote:

With that pathology report, there can be no question. It is breast cancer. All is crazy right now, I know. Once you see the oncologist and develop a plan, you will at least have a little structure to your life. Are you seeing a pediatric oncologist? Before telling my daughter, I think I would want to ask an expert how best to approach the subject. Keep breathing. Take one step at a time. With love,,,Judie

The world is so empty if one thinks only of mountains, rivers and cities; but to know someone who thinks and feels with us, and who, though distant is close to us in spirit, this makes the earth for us an inhabited garden. -Goethe
Dx 6/25/2007, IDC, 2cm, Stage IIb, Grade 2, 1/4 nodes, ER+/PR+, HER2-
BrandonMom
Joined: Sep 2008
Posts: 318
Apr 17, 2009 12:03 am BrandonMom wrote:

My son is a childhood cancer survivor.  You mention going to Children's Hospital of LA.  I'm not familiar with that one, but I know Children's Hospital of Orange County (CHOC) is supposed to be exceptional. Breast cancer does happen (rarely) in children.  So the good news is that it was diagnosed.  Since it is so rare, a lot of times breast cancer is not even considered, resulting in a delay in treatment.  Below are some resources that were helpful for me:

www.curesearch.org - Pediatric Oncology Group website.  Lots of information and overall a very helpful group.  Lots of good information and resources here.  You may want to give them a call.

www.candlelighters.org - A group to support parents of kids with cancer.  There are lots and lots of good resources there.

www.acor.org - look for the ped-onc mailing list.  It is an email list of parents with kids that have or have had cancer.  It was extremely helpful to me.

The hardest words I have ever heard, to this date, is my son's name (he was 4 at the time) and chemotherapy in the same sentence.  I can't tell you how much that hurt.  I went to pieces.   I wish that no other child ever had any type of cancer.  You can do this. It is hard, but you can get through this.  Your child will need you now more than ever.  When my son was diagnosed, it helped me to have a time of the day I would allow the pain to come in and I would cry, scream, etc.  For me, that was how I would start my day.  Then, I'd go take a shower and get on with my day.  Believe it or not, it worked for me,

Let us know how it goes.


Dx 8/22/2008, IDC, 5cm, Stage IIIa, Grade 3, 2/7 nodes, ER+/PR+, HER2+
mamakaren
Tucson, Az
Joined: Aug 2008
Posts: 224
Apr 17, 2009 01:29 am mamakaren wrote:

Hello, I have four children and one of them is a 9 year old girl. I can't imagine what your going through but I do know that with our God all things are possible. Please get a second opinion just to confirm that it's not a mistake. Hoping to God it is. I'm here for you to support you in all this madness. What is her name so i can name her at prayer group.

Many Blessings,

Karen 

"When we face what we fear... We become fearless"
Dx 1/22/2008, IDC, 2cm, Stage II, Grade 3, 0/10 nodes, ER-/PR-, HER2+
Wren
SE of the Emerald City
Joined: Sep 2007
Posts: 305
Apr 17, 2009 04:46 am Wren wrote:

I know that none of my words are adequate to express how sorry I am that you are going through this with such a young sweet child.

Please know that you are in my prayers. I will think of you every day and pray for your strength and peace on this journey that no child or parent should endure.

God Bless.

Diana63
Oh
Joined: Oct 2007
Posts: 513
Apr 17, 2009 05:06 am Diana63 wrote:

I wasn't going to read this because the thought of a child having BC is just to much, my heart goes out to you and your precious daughter. What is your daughters first name?

As for courage and will - we cannot measure how much of each lies within us, we can only trust there will be sufficient to carry through trials which may lie ahead.
Dx 10/6/2007, IDC, 5cm, Stage IIIa, Grade 3, 4/9 nodes, ER+/PR+, HER2-
lookingforw…
Joined: Nov 2007
Posts: 90
Apr 17, 2009 07:43 am lookingforward4more wrote:

I am a survivor with a 10 year old daughter and wanted you to know that you and your daughter are in my prayers. I am really sorry about her diagnosis, sending you many positive thoughts. Please lean on the wonderful women on this board to help her through whatever treatment plan you make.


Dx 11/13/2007, IDC, 3cm, Stage IIb, Grade 2, 2/24 nodes, ER+/PR+, HER2-
AnnaM
Virginia
Joined: Oct 2005
Posts: 1,668
Apr 17, 2009 08:04 am AnnaM wrote:

It looks like the wonderful women on this board have enfolded you in their gentle caring arms. I too wish you well and will keep you and your daughter in my prayers.

Anna

Hoolianama0…
Joined: Mar 2009
Posts: 71
Apr 17, 2009 10:29 am Hoolianama0508 wrote:

I am praying for you and your daughter.

I agree with springtime, we as a society have to push for better, earlier testing made available to everyone.

Fran Drescher was just on CNN online talking about why aren't we discovering cancer in stage 1 when it is in the most curable of the stages. (I am paraphrasing here, so I might not be stating it correctly).

I matter
Dx 3/27/2009, IDC, 5cm, Stage IIIa, Grade 3, ER-/PR-, HER2-
leaf
Joined: Dec 2005
Posts: 5,944
Apr 17, 2009 10:44 am leaf wrote:

What a shock for you and your daughter to go through. A collegue had a daughter who was diagnosed with ovarian cancer at about age 10.  We are all holding our hands out to you.

If you're going through hell, keep going-Winston Churchill
awb
Joined: Aug 2005
Posts: 2,764
Apr 17, 2009 11:25 am awb wrote:

My heart goes out to you and your DD. My DD had breast development at age 8 and started her period at age 10 and we have family history of bc (I have LCIS, my mom had ILC), so I have always worried about her future. The night before my breast biopsy, she came to me to show me a lump above her collarbone the size of a walnut (age 16 at the time). The pediatrician immediately gave her a breast exam when she learned of my situation. (and I feared everything from mono all the way to  lymphoma). Fortunately, it turned out to be only a swollen lymph node, but I know the fear you're feeling. I wonder that since she is so young for bc, if  specialists at St Judes (cancer hospital) would have any expertise or knowledge they could offer--(you could google St Judes for info)--it's always a good idea to get 2nd opinions, even 3rd. Praying for God's peace  for your family throughout this ordeal

Anne

"I don't know what the future holds, but I know who holds the future"
Dx 9/5/2003, LCIS, Stage 0, 0/0 nodes
otter
AL
Joined: Jan 2008
Posts: 3,948
Apr 17, 2009 12:20 pm otter wrote:

cjsocal, there really isn't anything I could say that would help to relieve the anxiety and fears you have right now.  I am sending hugs to you and your family, and especially to your daughter.

As others have said here, and as you know now from the pathology report, "infiltrating ductal carcinoma" is, indeed, breast cancer.  But, solid papillary carcinoma is an unusual type of breast cancer that often is not as aggressive as other types.  On the other hand, your daughter's tumor was determined to have no estrogen receptors or progesterone receptors (i.e., its growth is not driven by female hormones), and it does not over-express HER2.  So, it is considered "triple-negative".  Triple-negative breast tumors in adult women usually require chemotherapy, but I don't know what the treatment would be for a 10-year-old girl.

I don't know where you live, or where your daughter is being treated.  But, I second what others have said here:  Please take your daughter to a pediatric oncologist who has expertise in the treatment of solid tumors (not just childhood leukemia).  The best option would be to go to an NCI-designated comprehensive cancer center, or to another large research hospital that has the facilities and personnel to handle an unusual situation like the one your daughter is facing.

otter 


Dx 1/14/2008, IDC, 1cm, Stage I, Grade 2, 0/3 nodes, ER+/PR-, HER2-
LRM216
Marietta, GA
Joined: Feb 2009
Posts: 667
Apr 17, 2009 04:28 pm LRM216 wrote:

CJSocal - I cannot even find the words to convey my feelings to you and your precious daughter.  I thought my diagnose and hearing the words you have breast cancer was the most devastating thing I could have ever heard.  I was so wrong.  Hearing that your 10 year old daughter has breast cancer is far, far more devastating.  May God bless you all.  You will be in my thoughts and prayers.

Linda

I have been put on this frightening journey against my will, but I do not have to travel it alone.
Dx 2/23/2009, IDC, 1cm, Stage I, Grade 3, 0/3 nodes, ER-/PR-, HER2-
hollyann
Alpharetta, Ga
Joined: Nov 2007
Posts: 2,391
Apr 17, 2009 04:57 pm hollyann wrote:

CJSoCal, How are you today?.......Thinking of you and your precious daughter.......You all have been on my mind today.....Hope you are coping as well as you can at the moment......Just know that you are in my thoughts and prayers and all of us here are wishing good thougths for you.......

Hugs and love, Lucy
Dx 1/15/2007, IDC, 1cm, Stage Ib, Grade 1, 0/6 nodes, ER+/PR+, HER2-
vhqh
Joined: Sep 2007
Posts: 495
Apr 17, 2009 05:00 pm vhqh wrote:

This is such a difficult situation to be in!  I do want to offer you a ray of sunshine on the path report, a Ki67 of 3% is good, it is a measurement of how aggressive the tumor is and 3% would indicate lazy slow growing cancer cells.  Just for comparison, my Ki67 was 46%.

IDC, er+/pr +, her2 +++, stage IV
kim40
Halifax, NS
Joined: Dec 2008
Posts: 445
Apr 17, 2009 05:20 pm kim40 wrote:

Hi CJ

Just wondering how you and your family are today.  We are thinking of you.

((((HUGS))))

Kim - Breast Cancer may take the parts that make me a woman, but I will not allow it to take my life! FIGHT, FIGHT, FIGHT!!!
Dx 1/6/2009, IDC, 5cm, Stage IIIa, Grade 3, 14/19 nodes, ER+/PR+, HER2+
Binney4
Joined: Aug 2004
Posts: 4,617
Apr 17, 2009 05:50 pm Binney4 wrote:

Hello, Littlest SocalSmile

Welcome, welcome to our special Sisterhood. We are sorry for the sad parts of this diagnosis, but we sure are glad to know you and to surround you with our caring and experience. You sure are not alone.Cool As you'll notice, we are all doing well, thriving and fussing and cheering each other on. And you will do well too!

We always remind each other to take big deep breaths, just think about one day at a time, and remember that we'll all be here to help in every way we can.

Be well!Kiss
Binney

Mandy1313
the North East
Joined: Aug 2008
Posts: 521
Apr 17, 2009 06:14 pm, edited Apr 17, 2009 07:10 PM by Mandy1313 Mandy1313 wrote:

My heart and thoughts are with you.  Binney gave some good practical suggestions. I would add one other thing....buy a small tape recorder and ask the docs if you may tape their conversations. Most will say yes.  It is hard to remember everything they say later on and that will help you.

Also since your daughter is in an unusual situation, feel free to get second and third opinions from different medical centers.  Each doctor will have their own approach.  Find ones that you and your daughter are comfortable with. Don't be afraid to ask questions.  One nurse told me to say "is this medically necessary?" before each and every test. I was surprised how many of them were not medically necessary.

Your daughter is my heart and prayers and so are you and your spouse.

Mandy

otter
AL
Joined: Jan 2008
Posts: 3,948
Apr 17, 2009 06:56 pm otter wrote:

Hey, everybody--the posts have been coming from Mr. cjsocal:  "My wife and I have no idea what type, stage, etc..." and "My wife and I have been told that there will be a lot of doctors involved in this as it is so uncommon."  IMHO, he's a special father, to be posting here on behalf of his daughter (and wife).

cjsocal, please know that we are thinking of your daughter and your family. 

otter


Dx 1/14/2008, IDC, 1cm, Stage I, Grade 2, 0/3 nodes, ER+/PR-, HER2-
smithlme
Fort Bragg, CA
Joined: Dec 2007
Posts: 909
Apr 17, 2009 07:16 pm smithlme wrote:

My thoughts and prayers are with your family during this stressful time...

Linda

Dx 3/31/08, DCIS, ER+/PR- BRCA2+ Quit praying for a miracle...TODAY is the miracle.
Dx 3/28/2007, IDC, 2cm, Stage II, Grade 3, 0/9 nodes, ER-/PR-, HER2-
PT6
Joined: Apr 2009
Posts: 62
Apr 17, 2009 07:48 pm PT6 wrote:

OMG! There are several breast cancer consultants who will review the pathology and give you an second opinion. The first one is in the SF bay area. There is another one in San Diego but I can't find the link. I found the reference in a pamphlet about getting a breast cancer diagnosis from the American Cancer Assiociation.

 http://www.breastcancerconsultdr.com/index.html


Dx 4/10/2009, DCIS, , Grade 2, / nodes, ER+/PR+
LMDuncan
BC
Joined: Jan 2009
Posts: 518
Apr 17, 2009 08:51 pm LMDuncan wrote:

Just wanted to let you know I am thinking about you and your family.

((((HUGS)))) Lori

Lori
Dx 3/23/2008, IDC, 3cm, Stage IIIa, Grade 3, 17/23 nodes, ER+/PR-, HER2-
lizws
OK
Joined: Jul 2005
Posts: 2,636
Apr 17, 2009 08:55 pm lizws wrote:

Thinking of you all during this extremly stressful time. 

Hugs & Prayers,  Liz

Go through the day with hope and a smile..........
Dx 7/18/2005, ILC, 2cm, Stage IIa, Grade 2, 1/4 nodes, ER+/PR+, HER2-
mawhinney
Joined: Jun 2008
Posts: 630
Apr 17, 2009 09:07 pm mawhinney wrote:

You may be interested in www.caringbridges.org  It is free, personalized websites for anyone facing critical illness,  CaringBridge Connects Families and provdes support and encouragement. You can meet others facing major illnesses and you can post your story and pictures and updates for family members and friends.  A friend, who's 6 month old son, Cooper,  was diagnosed with a rare cancer, posts pictures and treatment information on www.caringbridges.org to keep family and friends informed.

You might also  take a look at www.mdanderson.com . MDAnerson is a major cancer treatment center in Texas. I have found much helpful info on their site.

www.chemocat.com If your daughter needs chemotherapy, you might want to get a copy of the book Chem Cat, written by a mother for her young daughter to help her understand the treatment her mother was going through. I recently read an article about the book but have not seen the book. It might be a help to your daughter. 

sweetpeas-n…
Joined: Apr 2009
Posts: 4
Apr 17, 2009 11:14 pm sweetpeas-nana wrote:

Hello Everyone,

My name is Beth and I am the grandmother of 10 year old in this disscussion. Her name is Hannah; but I have called her Sweet Pea since the day she was born. First, how can I say it, THANK YOU ALL SO MUCH for everything, your thoughts, your prayers, your suggestions, your care. Otter wrote that the writings were coming from Mr. jcsocal and Otter is correct, (although my daughter has been writing also) my son in law is a very special daddy and wants answers; He and my daughter are trying to understand all of it and help Hannah through it all.

We all have been in a cloud since Hannah was diagnosed with BC, never in a million years would we have thought that this could happen at 10. But it did and we are trying to make sense of it all.

They have both done a lot of research and now have some answers and understanding of what is happening.

There have been 7 patholigist's (up to this point) that have reviewed Hannah's test results and every one of them have come to the same diagnosis, IDC; and as far as treatment, in L.A. Childern's Hospital is one of the best, if they think she should go elsewhere they will send her. 

Hannah's Uncle has set up a web-site for her and I asked my daughter and son in law if I could post Hannah's web site here and they said it was O.K. If you want to visit and see what a special girl she really is, please go to her web site. OurLittleSweetPea.com. 

Also I have a question for anyone who may have the answer; Several wonderful organazations would like to do fundraisers for Hannah and they would like to use the Pink Breast Cancer Ribbon in the advertising; but we were told we have to have permission to use the Pink Ribbon and I have searched the internet and cannot find out where to get the permission.  If anyone knows where I can go would you please reply and let me know.

Thank you all for everything

Hannah's Nana and Papa

   

Godsgal
Joined: Jun 2008
Posts: 168
Apr 17, 2009 11:40 pm, edited Apr 17, 2009 11:41 PM by Godsgal Godsgal wrote:

OH MY ! !

I am soooo very sorry ..  This is not fair... She's just a baby.... GOD please help this family and allow this precious young jewel to live a long, full, and  happy life...

Be strong family and may GOD BLESS you Hannah.. 

Love, Peace, and Hope

webwriter
Extreme Southern, AL
Joined: Dec 2008
Posts: 535
Apr 18, 2009 01:27 am webwriter wrote:

Good Heavens. Is there no end to the nightmares this monster creates?

Sweetpea's Nana, the best I can find for you is this:

"The Canadian Breast Cancer Foundation states that,”The pink ribbon is the official mark of the Canadian Breast Cancer Foundation, and is licensed exclusively to us. This is not the case in other countries. We do enter licensing agreements with other organizations, authorizing them to use the official mark under specified conditions.”

http://www.alive.com/1526a4a2.php?subject_bread_cramb=351

I have seen several other references containing the same data. It is my understanding that in the United States, the pink ribbon breast cancer symbol is a part of the public domain, meaning no one owns it because it is a common symbol. HOWEVER, individual designs for the ribbon and the ensuing graphics CAN be copyrighted and often are. If you design your own, you are quite safe. Here too is a link to free downloadable ones. The designer asks only for a credit, but does not require payment or any other compensation for the use of her designs.

On a personal note, my own daughter has been SweetPea since the day she was born. This one hit home hard for all of us. We will be following Hannah's journey closely at our house. The site you all have created is a wonderful one. May it bring you all the support you will need in the times to come. May Hannah's strength and spirit be enduring and healthful. May all of you find peace and a rapid return to some semblance of normalcy. May all of us live to see the cure.

Bright Blessings,

Web

http://www.acoffeebreakcafe.com/CBC/blog/webbie/
Dx 11/24/2008, IDC, 1cm, Stage IIa, Grade 3, 1/19 nodes, ER+/PR+, HER2-
Binney4
Joined: Aug 2004
Posts: 4,617
Apr 18, 2009 01:48 am Binney4 wrote:

Ah, sweetpeas-nana, what a rich woman you are to have such beautiful grandchildren! Thank you for sharing them with us. As you can see, we're all very moved by SweetPea -- and by all of you, her family.

I'm wondering where you heard that about having to get permission to use a pink ribbon symbol? It's everywhere, and I've never seen any copyright registration. Many of us here have incorporated it into art projects that are publicly marketed -- mugs, tote bags, T-shirts, you-name-it -- without the slightest difficulty. As far as I can see, any of the many ribbons of various colors that represent different cancers or causes are certainly universals. Welcome to it! And do please keep us informed about fundraisers for Hannah -- we'd love to help.

Welcome to Hannah, to you, and to all your family -- you're not alone.
Hugs, prayers,
Binney

lazydaisy
Joined: Nov 2008
Posts: 50
Apr 18, 2009 01:48 am lazydaisy wrote:

Dear Beth and family,

I just wanted to send you all my love and to remind you that as Hannah's grandma, mom and dad -- be sure to let your friends and loved ones take care of you as well as Hannah. You need your strength and rest and energy to help your dear sweet pea, so don't hesitate to accept the many offers of assistance and support that must be coming your way from those who care about you.

xox

LRM216
Marietta, GA
Joined: Feb 2009
Posts: 667
Apr 18, 2009 01:52 am LRM216 wrote:

Sweetpeas Nana -  Thank you for sharing your website with us.  I will follow it very closely.  Hannah is truly a beautiful little girl, and my heart breaks for her and for her loved ones as you travel this path that was so unfairly dealt. I am 62 years old and was just recently diagnosed myself and have had such a very difficult time coming to terms with it.  In the course of just one sentence, one's life is changed forever, and one is suddenly faced with just how tenuous life really is for each of us.  Since hearing of Hannah, I must honestly say that I have been forced to realize just how fortunate I have been, in that I have lived to see both my daughters grow into women, to have their own children, and be able to share in all of their lives.  Hannah has forced me to look at the fears and apprehensions of my disease through newly opened eyes.  If I could take this from your Sweetpea, I truly would.  Please know that I pray fervently that when this nightmare you are all going through is over, that Hannah knows nothing but a million happy tomorrows. 

LRM216

I have been put on this frightening journey against my will, but I do not have to travel it alone.
Dx 2/23/2009, IDC, 1cm, Stage I, Grade 3, 0/3 nodes, ER-/PR-, HER2-

Page 3 of 14 (416 results)

© 2009 Breastcancer.org. All rights reserved.