Watching a Meningioma Brain Tumor

Posted by robinem @robinem, Feb 8, 2018

I've just been diagnosed with a 2cm meningioma tumor on the right front of my head. I am 59 years old and the surgeon has told me I will need to "do something" with my tumor someday since I am younger. What is the benefit of waiting?

Interested in more discussions like this? Go to the Brain Tumor Support Group.

@lindajean

A brief update......I just had an MRI and once again, no change in my 2 Meningioma's.......Now 17 years of Watch and Wait with NO needed surgery!!!!! Just wanted to share so others are not so afraid if they are on a watch and wait for years 🙂

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Happy to hear this great news! Hopeful!

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@cscmaryann

I have never heard of a gamma tile. I will look that one up.

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@cscmaryann, Gamma Knife is a type of stereotactic radiosurgery (STS) used to treat tumors, veins that have developed differently than usual and other differences in the brain.

Similar to other types of stereotactic radiosurgery (STS), Gamma Knife radiosurgery is not a standard surgery because there is no cut, called an incision You can read more here: https://www.mayoclinic.org/tests-procedures/brain-stereotactic-radiosurgery/about/pac-20384679

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@ninha06

Hi @colleenyoung, unfortunately, I have. Last October I was incidentally diagnosed with a 2.5cm meningioma behind my right eye, thank God it is not pressing my optic nerve, it shows a bit of calcification, so I hope it grows very slowly if at all. I'm asymptomatic and on surveillance till April, but I am freaking out, I am suffering with anxiety and depression. I am soooo afraid of the surgery that I am thinking about GammaKnife instead. I'm in Canada so here is more complicated to choose your physicians and treatments since the healthcare system is public. Could someone tell me more about the pros & cons of Gamma Knife? Thanks.

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@ninha06, here's more information about gamma knife available in Toronto, Canada, where they have great specialists in brain surgery at the Krembil Barin Institute, part of the University Health Network (UHN) https://www.uhn.ca/Krembil/Clinics/Gamma_Knife

You might also be interested in reading the comments on these related discussions about Gamma knife
https://connect.mayoclinic.org/group/brain-tumor-support-group/?search=gamma+knife#discussion-listview
You might start here:
- - Stereotactic Radiosurgery Surgery (Gamma or Cyberknife) for Meningioma: https://connect.mayoclinic.org/discussion/gamma-knife-radio-surgery-for-meningioma/

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@brankintx

I saw my oncologist yesterday. Thankfully the area where the gamma tile was placed worked no new growth i was told the area behind my eye was previously radiated was not surgically removed because the neurosurgeon thought it would cause too much damage i asked if there was something i could do to slow growth he told me to ask my neurologist

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I have never heard of a gamma tile. I will look that one up.

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@colleenyoung

@ninha06, welcome. Have you also been diagnosed with a meningioma? How are you doing?

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Hi @colleenyoung, unfortunately, I have. Last October I was incidentally diagnosed with a 2.5cm meningioma behind my right eye, thank God it is not pressing my optic nerve, it shows a bit of calcification, so I hope it grows very slowly if at all. I'm asymptomatic and on surveillance till April, but I am freaking out, I am suffering with anxiety and depression. I am soooo afraid of the surgery that I am thinking about GammaKnife instead. I'm in Canada so here is more complicated to choose your physicians and treatments since the healthcare system is public. Could someone tell me more about the pros & cons of Gamma Knife? Thanks.

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@ninha06

Hi Linda, I glad to hear it. What are the sizes and location of your meningiomas? Take care.

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@ninha06, welcome. Have you also been diagnosed with a meningioma? How are you doing?

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@lindajean

A brief update......I just had an MRI and once again, no change in my 2 Meningioma's.......Now 17 years of Watch and Wait with NO needed surgery!!!!! Just wanted to share so others are not so afraid if they are on a watch and wait for years 🙂

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Hi Linda, I glad to hear it. What are the sizes and location of your meningiomas? Take care.

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@mkoch

I am surprised to hear you've had 4 craniotomies. I didn't know that was an option. I had a craniotomy 6 months ago for a meningioma that was almost 3 cm. and close to my optic nerve. I also have 2 other meningiomas that I need to deal with (now that I'm 6 months post surgery I'm mentally up to dealing with the other two) and I thought my only option was radiation, which scares me more than another craniotomy. Good wishes for you as you continue to navigate your health issues.

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You might want to look into proton therapy radiation treatments at Mayo Rochester or elsewhere. An option apart from crainiotomy.

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I saw my oncologist yesterday. Thankfully the area where the gamma tile was placed worked no new growth i was told the area behind my eye was previously radiated was not surgically removed because the neurosurgeon thought it would cause too much damage i asked if there was something i could do to slow growth he told me to ask my neurologist

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@brankintx

I am currently on watch wait for four meningioma that were left behind. I have had four Crainiotomy one being a cancerous tumor grade 3. They placed gamma tile in hopes of keeping the meningioma from coming back. I just had an MRI that showed minimal growth, I see my oncologist tomorrow to see what his plan is. This all started in 2015 for a large tumor that had to come out six years later I had to have another one removed i had proton radiation after each surgeries then 11 months later was my third craniotomy. I have had 1 seizure and memory loss but that could be age related. I am 71 I still have the shooting pains in my scalp occasional headaches I feel off balance. But im alive and it could have been much worse its in Gods hands and I pray they find a way for all of us to overcome this

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I am surprised to hear you've had 4 craniotomies. I didn't know that was an option. I had a craniotomy 6 months ago for a meningioma that was almost 3 cm. and close to my optic nerve. I also have 2 other meningiomas that I need to deal with (now that I'm 6 months post surgery I'm mentally up to dealing with the other two) and I thought my only option was radiation, which scares me more than another craniotomy. Good wishes for you as you continue to navigate your health issues.

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