After 20 years of sporatic symptoms (right side
numbnessNumbness and tingling & 2 cases of optic
neuritisGuillain-barre syndrome
Optic neuritis
Peripheral neuropathy) I was DX last year with MS. Other "conditions" although not related to the MS include moderate depression, headaches (including migraines) & hypothyroidism. Had MRI done in 1988 (in conjunction with the
numbnessNumbness and tingling) that showed 4 lesions, possibly related to MS, spinal fluid was negative. An incidental finding of a
venousDeep venous thrombosis
Deep venous thrombosis, iliofemoral
Intravenous
Intravenous pyelogram
Intravenous pyelogram (ivp)
Pulmonary arteriovenous fistula
Pulmonary embolus
Stasis dermatitis and ulcers
Varicose vein therapy
Venous blood clot
Venous insufficiency anomaly was mentioned on the MRI last year. No "enhancing" lesions were identified, but about 8 "old" lesions were found (brain & spine). Followup MRI done Feb 6, 09. MS lesions are
stableStable angina
Unstable angina (no new ones & no enhancing), however 2 of 3 page radiologist report about a 7 mm
cavernousHemangioma malformation that is now adjacent to the venous anomaly.
Here is the quote from the summary findings of the radiology report...
"Developmental venous anomaly draining parenchyma at the right insular/suminsular region and right basal ganglia region. This is associated with a small (7mm) carernous vascular malformation involving adjacent portions of the very posterior aspect of the posterior limb of the right internal capsule and right thalamus. The signal changes related to the cavernous malformation have increased in size, suggesting that there has been interval episode of minor bleeding at this lesion, potentially subacute, but with out evidence of findings to suggest acute hemorrhage or adjacent reactive edema."
MS Dr. referred films to the neuro interventionalist in group. After 2 weeks of waiting I got a call from the nurse stating that the interventionalist said "it is not emergent, & is inoperable due to its location. I can make an apt with him if I want more information". The soonest they can get me in is March 11, so I was hoping to get some info here. Since thalamus plays a part in all of my "symptoms" and other "conditions" could the CCM be causing all my issues & the MS be a wrong dx? Currently taking copaxone, but would like to stop if not needed.