Primary neurolymphomatosis is the direct infiltration of lymphomatous neoplastic cells into nerve roots and/or peripheral nerves. A 67-year-old man had a 24-month history of progressive and severe left lower limb neuropathic pain, ipsilateral ankle dorsiflexion weakness and gait disturbance. Gadolinium-enhanced MRI showed thickening and enhancement of the cauda equina, L5, S1 and S2 nerve roots. 18 Fluorodeoxyglucose positron emission tomography showed concordant hypermetabolism. L5 nerve root biopsy confirmed diffuse large B-cell lymphoma. One cycle of rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) chemotherapy resulted in remission, but this was not sustained. Primary neurolymphomatosis is rare and diagnostically challenging, and often the diagnosis is delayed. While biopsy is the gold standard for diagnosis, neuroimaging helps to characterise lesions and to determine the feasibility of biopsy.
Keyphrases
- diffuse large b cell lymphoma
- positron emission tomography
- neuropathic pain
- computed tomography
- ultrasound guided
- lower limb
- fine needle aspiration
- spinal cord
- epstein barr virus
- peripheral nerve
- pet ct
- spinal cord injury
- contrast enhanced
- induced apoptosis
- magnetic resonance imaging
- low dose
- pet imaging
- magnetic resonance
- cell proliferation
- oxidative stress
- signaling pathway
- early onset
- ulcerative colitis
- rheumatoid arthritis
- endoplasmic reticulum stress
- silver nanoparticles
- pi k akt