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Hi Gang,

Hoping that you can help me out here. A couple of years ago, I was told that

there was a " mass found in my chest " during a CT scan. My endo suggested

surgery to remove this mass and sent me to a cardiovascular surgeon who also

thought it was a good idea. Of course I wanted a second opinion and flew

from Pittsburgh to Houston (MD ) and got a second opinion of a

thyroid specialist/endo/ oncologist there. An entire board of specialists

(nuc med, oncologists, endos and surgeons) reviewed my case. While I was in

Houston, I had another CT scan and many ultrasounds. It was decided upon

that the mass in my chest was my Thymus gland. This area never " lights up "

on WBS using RAI although I have had lung involvement in the past

Now, I have read several posts from some of you folks that mentioned similar

surgeries performed to remove your thymus. Was there malignancies found

within your thymus? I understand that our thymus is a gland typically used

in childhood and that it should actually shrink during adult life. It seems

to me that several of us thyca people have enlarged thymuses. Is there a

reason our thymus might be enlarged (perhaps due to RAI, etc.?)? I guess what

I'm getting at is.....my second opinion (which was very well reviewed)

expressed NO REASON to have this surgery. They would have had to crack open

my chest as if I were having open heart surgery only to remove an organ that

is supposed to be there. If anyone else has had similar experiences, PLEASE

respond as there are a couple of us who have this situation.

NOW, I have a mass in the left side of my neck. I feel that this is a muscle

which has stiffened due to 3 large therapeutic doses of RAI. Again, my endo

is suggesting surgery. I will see my surgeon this week. After that, I will

fly to Houston again to get a 2nd opinion. I really don't believe that this

mass is thyca (although I am not a doctor). However, I have lost 50 pounds

over the last year (Thank Heavens!) and my neck is no longer hidden by my

multiple chins! hehehehe Therefore, this mass has probably been there all

along yet we just didn't notice it as much. Still, better safe than sorry. I

suppose they are probably concerned about Hurtle Cell involvement, etc. What

are the chances of having Hurthle cell involvement when initial dx was Pap

Carcinoma?

SIGH!!!! All this garble in my head is making me tired! heheh Please respond

as I am looking for some advice quickly. :) I may be on a plane to Houston

as early as next week!!!

Love,

Audra

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Hi again Audra,

I am waiting and hoping you get a responce because I too have posted a

similar question over the past few months with only a responce from

(who has the reverse problem -- a radiated thymus as a child

which likely caused her thyca). Perhaps there are only a few of us

with this problem.

I'm seeing my surgeon next week and have this major chest-cracking

surgery scheduled (tentatively) for Sept 4th. At first I didn't want

to accept that I needed surgery (as I wrote to you before), but

everyone I have consulted with says I have to do it because that's the

only way to find the cause. Lousy isn't it!

Please keep us informed as to what you are advised as I'm in the same

boat.

Rita

tt Feb '99 (3.5cm pap encapsulated, 9 lymph node mets, some tall

cells)

RAI Apr '99 150mci

RAI May '00 220mci

4 CT chest scans (thymus has grown " larger & denser " )

> Hi Gang,

>

> Hoping that you can help me out here. A couple of years ago, I was

told that

> there was a " mass found in my chest " during a CT scan. My endo

suggested

> surgery to remove this mass and sent me to a cardiovascular surgeon

who also

> thought it was a good idea. Of course I wanted a second opinion and

flew

> from Pittsburgh to Houston (MD ) and got a second opinion of

a

> thyroid specialist/endo/ oncologist there. An entire board of

specialists

> (nuc med, oncologists, endos and surgeons) reviewed my case. While I

was in

> Houston, I had another CT scan and many ultrasounds. It was decided

upon

> that the mass in my chest was my Thymus gland. This area never

" lights up "

> on WBS using RAI although I have had lung involvement in the past

>

> Now, I have read several posts from some of you folks that mentioned

similar

> surgeries performed to remove your thymus. Was there malignancies

found

> within your thymus? I understand that our thymus is a gland

typically used

> in childhood and that it should actually shrink during adult life.

It seems

> to me that several of us thyca people have enlarged thymuses. Is

there a

> reason our thymus might be enlarged (perhaps due to RAI, etc.?)? I

guess what

> I'm getting at is.....my second opinion (which was very well

reviewed)

> expressed NO REASON to have this surgery. They would have had to

crack open

> my chest as if I were having open heart surgery only to remove an

organ that

> is supposed to be there. If anyone else has had similar

experiences, PLEASE

> respond as there are a couple of us who have this situation.

>

> NOW, I have a mass in the left side of my neck. I feel that this is

a muscle

> which has stiffened due to 3 large therapeutic doses of RAI. Again,

my endo

> is suggesting surgery. I will see my surgeon this week. After that,

I will

> fly to Houston again to get a 2nd opinion. I really don't believe

that this

> mass is thyca (although I am not a doctor). However, I have lost 50

pounds

> over the last year (Thank Heavens!) and my neck is no longer hidden

by my

> multiple chins! hehehehe Therefore, this mass has probably been

there all

> along yet we just didn't notice it as much. Still, better safe than

sorry. I

> suppose they are probably concerned about Hurtle Cell involvement,

etc. What

> are the chances of having Hurthle cell involvement when initial dx

was Pap

> Carcinoma?

>

> SIGH!!!! All this garble in my head is making me tired! heheh Please

respond

> as I am looking for some advice quickly. :) I may be on a plane to

Houston

> as early as next week!!!

>

> Love,

> Audra

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Guest guest

Hi again Audra,

I am waiting and hoping you get a responce because I too have posted a

similar question over the past few months with only a responce from

(who has the reverse problem -- a radiated thymus as a child

which likely caused her thyca). Perhaps there are only a few of us

with this problem.

I'm seeing my surgeon next week and have this major chest-cracking

surgery scheduled (tentatively) for Sept 4th. At first I didn't want

to accept that I needed surgery (as I wrote to you before), but

everyone I have consulted with says I have to do it because that's the

only way to find the cause. Lousy isn't it!

Please keep us informed as to what you are advised as I'm in the same

boat.

Rita

tt Feb '99 (3.5cm pap encapsulated, 9 lymph node mets, some tall

cells)

RAI Apr '99 150mci

RAI May '00 220mci

4 CT chest scans (thymus has grown " larger & denser " )

> Hi Gang,

>

> Hoping that you can help me out here. A couple of years ago, I was

told that

> there was a " mass found in my chest " during a CT scan. My endo

suggested

> surgery to remove this mass and sent me to a cardiovascular surgeon

who also

> thought it was a good idea. Of course I wanted a second opinion and

flew

> from Pittsburgh to Houston (MD ) and got a second opinion of

a

> thyroid specialist/endo/ oncologist there. An entire board of

specialists

> (nuc med, oncologists, endos and surgeons) reviewed my case. While I

was in

> Houston, I had another CT scan and many ultrasounds. It was decided

upon

> that the mass in my chest was my Thymus gland. This area never

" lights up "

> on WBS using RAI although I have had lung involvement in the past

>

> Now, I have read several posts from some of you folks that mentioned

similar

> surgeries performed to remove your thymus. Was there malignancies

found

> within your thymus? I understand that our thymus is a gland

typically used

> in childhood and that it should actually shrink during adult life.

It seems

> to me that several of us thyca people have enlarged thymuses. Is

there a

> reason our thymus might be enlarged (perhaps due to RAI, etc.?)? I

guess what

> I'm getting at is.....my second opinion (which was very well

reviewed)

> expressed NO REASON to have this surgery. They would have had to

crack open

> my chest as if I were having open heart surgery only to remove an

organ that

> is supposed to be there. If anyone else has had similar

experiences, PLEASE

> respond as there are a couple of us who have this situation.

>

> NOW, I have a mass in the left side of my neck. I feel that this is

a muscle

> which has stiffened due to 3 large therapeutic doses of RAI. Again,

my endo

> is suggesting surgery. I will see my surgeon this week. After that,

I will

> fly to Houston again to get a 2nd opinion. I really don't believe

that this

> mass is thyca (although I am not a doctor). However, I have lost 50

pounds

> over the last year (Thank Heavens!) and my neck is no longer hidden

by my

> multiple chins! hehehehe Therefore, this mass has probably been

there all

> along yet we just didn't notice it as much. Still, better safe than

sorry. I

> suppose they are probably concerned about Hurtle Cell involvement,

etc. What

> are the chances of having Hurthle cell involvement when initial dx

was Pap

> Carcinoma?

>

> SIGH!!!! All this garble in my head is making me tired! heheh Please

respond

> as I am looking for some advice quickly. :) I may be on a plane to

Houston

> as early as next week!!!

>

> Love,

> Audra

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Share on other sites

Guest guest

Hi again Audra,

I am waiting and hoping you get a responce because I too have posted a

similar question over the past few months with only a responce from

(who has the reverse problem -- a radiated thymus as a child

which likely caused her thyca). Perhaps there are only a few of us

with this problem.

I'm seeing my surgeon next week and have this major chest-cracking

surgery scheduled (tentatively) for Sept 4th. At first I didn't want

to accept that I needed surgery (as I wrote to you before), but

everyone I have consulted with says I have to do it because that's the

only way to find the cause. Lousy isn't it!

Please keep us informed as to what you are advised as I'm in the same

boat.

Rita

tt Feb '99 (3.5cm pap encapsulated, 9 lymph node mets, some tall

cells)

RAI Apr '99 150mci

RAI May '00 220mci

4 CT chest scans (thymus has grown " larger & denser " )

> Hi Gang,

>

> Hoping that you can help me out here. A couple of years ago, I was

told that

> there was a " mass found in my chest " during a CT scan. My endo

suggested

> surgery to remove this mass and sent me to a cardiovascular surgeon

who also

> thought it was a good idea. Of course I wanted a second opinion and

flew

> from Pittsburgh to Houston (MD ) and got a second opinion of

a

> thyroid specialist/endo/ oncologist there. An entire board of

specialists

> (nuc med, oncologists, endos and surgeons) reviewed my case. While I

was in

> Houston, I had another CT scan and many ultrasounds. It was decided

upon

> that the mass in my chest was my Thymus gland. This area never

" lights up "

> on WBS using RAI although I have had lung involvement in the past

>

> Now, I have read several posts from some of you folks that mentioned

similar

> surgeries performed to remove your thymus. Was there malignancies

found

> within your thymus? I understand that our thymus is a gland

typically used

> in childhood and that it should actually shrink during adult life.

It seems

> to me that several of us thyca people have enlarged thymuses. Is

there a

> reason our thymus might be enlarged (perhaps due to RAI, etc.?)? I

guess what

> I'm getting at is.....my second opinion (which was very well

reviewed)

> expressed NO REASON to have this surgery. They would have had to

crack open

> my chest as if I were having open heart surgery only to remove an

organ that

> is supposed to be there. If anyone else has had similar

experiences, PLEASE

> respond as there are a couple of us who have this situation.

>

> NOW, I have a mass in the left side of my neck. I feel that this is

a muscle

> which has stiffened due to 3 large therapeutic doses of RAI. Again,

my endo

> is suggesting surgery. I will see my surgeon this week. After that,

I will

> fly to Houston again to get a 2nd opinion. I really don't believe

that this

> mass is thyca (although I am not a doctor). However, I have lost 50

pounds

> over the last year (Thank Heavens!) and my neck is no longer hidden

by my

> multiple chins! hehehehe Therefore, this mass has probably been

there all

> along yet we just didn't notice it as much. Still, better safe than

sorry. I

> suppose they are probably concerned about Hurtle Cell involvement,

etc. What

> are the chances of having Hurthle cell involvement when initial dx

was Pap

> Carcinoma?

>

> SIGH!!!! All this garble in my head is making me tired! heheh Please

respond

> as I am looking for some advice quickly. :) I may be on a plane to

Houston

> as early as next week!!!

>

> Love,

> Audra

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