3/9/06 large convexity meningioma over parietal lobe excised. Per operative report all tumor removed but dura margin not resected but heavily coagulated. Referred for
radiationCystitis - noninfectious
Radiation therapy therapy.
3/22/05
radiationCystitis - noninfectious
Radiation therapy oncologist recommended therapy.
4/4/06
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc post op MRI..conclusion 3.9cm ap oblique x 2.2 cm tranverse oblique residual.
5/17/06 MRI for treatment planning...conclusion...no convincing evidence of residual or
recurrentRecurrent cystitis tumor. Some enchancement around margins.
Therapy was canceled by
radiationCystitis - noninfectious
Radiation therapy oncologist to reassess.
Discussion one week later she said the options were to irradiate now, but she would narrow the field; or to have MRIs every 2 months and treat if regrowth. She would review all and we would talk the next week.
2nd dicussion.."no wrong decision". Treatment would be the same and could be done now or MRI every 4 months and watch.
Question: The results of the 2 MRIs seem so radically different and the decision would be based on what is or isn't left. Don't understand how a residual tumor of this size would magically disapper in a
littleLittle noses decongestant
Little tummys more than a month. Surgeon merely states he left some...has no further input. Radiation oncologist does not offer opinion one way or the other. Both options ok.
Also said after radiation if recurrence surgery is the only option. If there is significant tumor left we would choose radiation now. If not would probably watch and hope to avoid doing it; but would still have that option open. No one seems to want to discuss the difference in these 2 MRIs. Suggestions to help with decision? Thx
I had a Meningioma resection in 2002 with ~ 5% of the lesion remaining on my optic nerve. I also have an acoustic Neuroma on my right cranial nerve. Both were radiated using Fractionated Stereotatic Radiation. The remaining 5% has not grown since 2-2006 and the AN has reduced in volume by 25%. That’s the good news. The treatment is not without it’s side effects and complications. I have experienced occasional bouts of facial nerve issues and the radiation took over 18 months to stop the growth of my tumor. I have been diagnosed with Neurofibromatosis Type II, which makes my case more complicated. According to Dr. David Andrews (Jeffferson U., Philly) study the NF tumor cells may be more resistant to STS.
…best regards