Hello,
I have MDS.
I developed L'Hermittes, went to Neuro and had MRI. Reported normal. L'Hermittes abated but, got tingling and tightness in feet and then to knees. Became ataxic. Returned to Neuro and had MRI. Report normal. Neuro thought he saw increased signal in posterior column cervical cord. Told to return in 2months.
Symptoms rose to my abdomen. Haematologist did a LP and MRI. CSF had increased protein and positive 14-3-3 protein. MRI showed definite signal change in posterior column. Decided to watch and wait. Had a few falls and admitted to hospital.
O/E positive Rombergs, couldn't tandem gait, nonresponsive Plantars, loss of vibration to T3, brisk ankle, knee reflexes with hypertonicity, loss of proprioception to the ankle. Upper limbs normal.
Hb low, neuts low, lymphs low, platelets low. Liver enzymes high, ESR high, ANA positive 320, Vit D low, zinc high, copper low, ceruloplasmin low, ferritin high. Urinary protein high, urinary copper high. History of low B12 now fixed.
Diagnosed copper deficiency induced myelopathy and cytopenia (not MDS). Started on S/C copper 2mgs twice a day . Serum copper normalised. Cytopenias better with slightly low WCC remaining.
Haematologist queries the diagnosis because of positive 14-3-3 protein in CSF, positive BMB for MDS (still) and neuro problem progressing despite copper replacement. Have new paraesthesia of left upper arm and right side of face. He thinks I ve an infective or autoimmune process. I was fit and well until I got severe atypical (Mycoplasma) pneumonia in 03 and have been sick since.
Could I have your opinion please?
Thank you.