Painful lumbosacral plexopathy: a case report.
Edvard Ehler1, Oldřich Vyšata, Radek Včelák
1From the Department of Neurology (EE), Regional Hospital and Faculty of Health Studies, University of Pardubice; Department of Neurology (OV), University Hospital Hradec Králové; Department of Radiology (RV), Regional Hospital Pardubice; and Department of Neurology (LP), Health Centre Rychnov nad Kneznou, Czech Republic.
A rare case of painful lumbosacral plexopathy (LSP) in a 64-year-old man showed severe muscle weakness. Electromyography and MRI confirmed axonal lesions, suggesting an autoimmune cause for this lumbar plexus disorder.
Area of Science:
- Neurology
- Neurophysiology
Background:
- Lumbosacral plexus disorders (LSP) are common and require thorough neurological examination, including electromyography (EMG) and magnetic resonance imaging (MRI), for diagnosis.
- Differential diagnosis for LSP encompasses metabolic, oncological, inflammatory, ischemic, and autoimmune conditions.
- Assessing muscle paresis, sensory deficits, pain, and spinal abnormalities is crucial for evaluating LSP.
Observation:
- A 64-year-old male presented with acute onset of painful LSP.
- Electromyography revealed axonal lesions, while MRI indicated plexus affliction distal to the nerve roots.
- The patient experienced severe muscle paresis in the femoral and obturator nerve distributions.
Findings:
- The case highlights a rare presentation of painful lumbosacral plexopathy.
- Electromyography findings were consistent with an axonal type of nerve injury.
- Gradual remission of symptoms occurred over a 3-month period.
Implications:
- The presumed autoimmune etiology in this case expands the understanding of LSP causes.
- This case underscores the importance of considering autoimmune disorders in the differential diagnosis of painful plexopathies.
- Further research into autoimmune mechanisms underlying LSP is warranted.
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