51 yr old
womanWomen's way diagnosed with demyelinating disease in 2002 (Multiple Sclerosis). Also have ulcerative
colitisColitis
Irritable bowel syndrome
Ischemic colitis
Necrotizing enterocolitis
Salmonella enterocolitis
Ulcerative colitis,optic
neuritisGuillain-barre syndrome
Optic neuritis
Peripheral neuropathy,iritis, arthritis (not
painfulPainful menstrual periods). All blood tests came back negative i.e. ANA, Rheumatoid, etc. MRI shows Multiple small foci of
brightBright beginnings FLAIR signal in the subcortical white matter of both hemispheres in a relatively symmetric distribution. No mass effect or midline shift. No
extraExtra strength mylanta calci tabs
Extra strength pain relief-axial mass or fluid collection is demonstrated. Paranasal sinuses & temporal bones appear normal. Posterior fossa is unremarkable. No abnormal enhancement is present post gadolinium. Impression: Several small nonspecific bright T2 subcortical lesions. This might be secondary to her demyelinating disease. I have hypo reflexes (knee). Spasticity in both legs more so right leg and right hand. I don't have lesions in the Dawson fingers or corpus callosum.
Symptoms-balance,spasticity,chronic optic neuritis,weak legs & rt. arm,fatigue. New symptom-headaches (over eyes or top of head). Sometimes daily headaches now. Received monthly solumedrol for 1 yr till it didn't work anymore, then Novantrone for 1 yr (didn't work). Took Betaseron (1 1/2 yr.) didn't work. RX includes sulfasalazin, Neurontin, Nabumetone,Baclofen,Trazadone(to help sleep),Cenestin (HRT). What could secondary disease be. Neurologist thinks I am part MS and part Lupus. Is that possible or what could I have. Thank you.
I am sorry to hear of your symptoms which are much like mine were aside from optic neuritis. Our brain reports are almost identical.
Your symptooms and your pathology truly resemble Lyme disease. Lyme disease can present those lesions and often times Lumbar Punctures in Lyme patients show no bands.
Please be advised that the blood tests, such as the Elisa, commonly used are known to be non-specific and worthless. IGENEX Labs in California are always complimentary. Depending upon your locale, I would, suggest that you find yourself a physician who specializes in Lyme disease. You can attain one by going to lymenet.org.
Hope I helped. I had the same problems, by in large, that you have.
Peace.
Heres my MRIS..
BRAIN:
FINDINGS:
There is no MRI evidence of midline shift or mass effect. Multiple round to ovoid foci of increased T2 weighted signal are noted in the periventricular and deep white matter of both cerebral hemispheres. Some foci within the centrum semi-ovale are oriented perpendicular to the plane of the corpus callosum and cingulate gyrus, suspicious for MS plaques. More ill-defined increased T2 weighted signal is noted in the periventricular white matter. Faint nodular areas of increased T2 weighted signal are noted within the corpus callosum. A small, 3-4 mm ovoid focus of increased T2 weighted signal is seen within the posterior aspect of the left middle cerebellar peduncle.
After IV contrast, at least five of the presumed plaques appear to enhance, the largest seen in the right frontal white matter, measuring 8 mm in maximum AP dimension.
Normal signal void is demonstrated in the major vasculature at the base of the brain. Visualized paranasal sinuses appear clear.
IMPRESSION:
Multiple round to ovoid foci of increased T2 weighted signal in the periventricular and deep white matter of both cerebral hemispheres, as well as within the left middle cerebellar peduncle and corpus callosum. Several lesions appear to enhance after IV contrast. Findings are non-specific, but are suspicious for MS plaques. Other etiologies, such as Vasculitis or Lyme disease, could produce similar findings. Clinical correlation advised.
CERVICAL SPINE:
FINDINGS:
The bone marrow signal appears well maintained. There is reversal of normal cervical lordosis. Disc space heights appear well maintained. Not acute verterbral body compression fracture is demonstrated. The carniocervical junction appears unremarkable.
Saggital STIR sequence shows extensive signal abnormality within the cervical spinal cord, throughout the entire cervical spine. No cord compression is demonstrated. The neural canal regions appear ample in size.
Gladolinium-enhanced imaging shows no abnormal enhancement.
IMPRESSION:
Extensive areas of hyperintense signal abnormality within the cervical spinal cord, most consistent with a demyelinating process. No enhancement was demonstrated. Please see report from MRI of the brain.
Wow. This raises questions for to then. I wonder. Weird how there can be multiple lesions, symptoms and it not be a known etiology.
I just wanted to help. I hope that you can find answers.
Peace,
JCmcc.
It does seem unfair that these diseases come not in single spies but in battalions!