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Need Help With Translation of Mri Report

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asurvivor

New User, Becoming EHEALTHy
Joined: 15 Jan 2004
Posts: 3
Location: Northern California
Need Help With Translation of Mri Report
Posted: 01-16-04 00:26am

Rolling Eyes I have had ms since I was a teenager but did not receive diagnosis until I was 43 years old. This is because I was in the military health system and seldom saw the same doctor twice in succession. In 1983 I received a definite diagnosis and this has been confirmed more than once. Recently I moved to a new town and had to find a new neurologist from the yellow pages. He wants to reinvent the wheel, and has not read the history I brought to him. He recently ordered an mri and I reluctantly complied. Today I visited him for the results and he told me that he is not sure I have ms. He would like to do more tests. I asked for a copy of the mri report and in it I saw this: "multiple foci of abnormal high t2 signal density within the periventricular white matter of both cerebral hemispheres... Differential diagnosis would include a demyelinating process such as multiple sclerosis..." (the most prominent of the problems which have been seen on several mris are in the area of the left globus pallidus; the first time it was discovered was in 1982 on a cat scan and at that time it was described as being in the internal capsule) I intend to find another neurologist with whom I can communicate better, but I am hoping that a medical professional will read the above and give me a translation of the area of in quotes.
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litekpr2

New User, Becoming EHEALTHy
Joined: 20 Feb 2004
Posts: 23
Location: USA

Posted: 02-20-04 02:49am

I'm not a medical professional but I think I can tell you the gist of what the report said. It sounds very similar to the report I got after my first mri, from which I was diagnosed with ms.

"multiple foci" means more than one lesion or "abnormal spot" in the brain...Abnormally high density (or thickness)... Found within the white matter of the brain on both sides (left and right)...

Then the kicker is how the radiologist read the films and offered his opinion: (and this is the part which was almost identically worded in my own first mri report): "differential diagnosis would include a demyelinating process such as multiple sclerosis..." with an mri report similar to yours, my diagnosis was confirmed by the radiologist, my family doctor who happened to be an internist, and the neurologist she consulted with. After I was referred to a neurology specialist, he read the films and concurred. A couple of years later, I had to change neurologists because of insurance changes, and that new neurologist confirmed the diagnosis also.

I don't understand why the doctor is hesitant to make a ms diagnosis, unless he is afraid of going out on a limb (for legal liability purposes). What kind of "more tests" does he want, anyway?
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asurvivor

New User, Becoming EHEALTHy
Joined: 15 Jan 2004
Posts: 3
Location: Northern California
Need Help With Mri Translation
Posted: 02-20-04 15:16pm

:p thanks for the response to my question. I took action last week, by changing to a new neurologist, but not before I told the old one what a 'twerp' I thought he was. I believe he was simply too young and inexperienced with ms to deal with the complex history of the course of the disease as it applies to me. My new neurologist specializes in ms cases and had no problem figuring out that I do have ms and suggested that I get on the "c" injections soon. The 2-1/2 years that I spent on avonex was great for the first two years and then for some reason I started having bad "flu-like" symptoms for most of the seven days between injections. I finally quit avonex and have been without any of the major medicines for the past three years. Since I have been having some rather serious symptoms recently, I am considering going on the copaxone.
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litekpr2

New User, Becoming EHEALTHy
Joined: 20 Feb 2004
Posts: 23
Location: USA

Posted: 02-21-04 00:12am

I have been on copaxone since february 1999. It has worked very well for me, with virtually no side effects except perhaps a mild stinging or itching sensation at the injection site which lasted only a few minutes.

Copaxone is the only one of the abcr drugs I can take, and luckily it seems to be working very successfully.

Good luck to you.
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