Volume 48, Issue 2 pp. 301-305
Case of the Month

Lower motor neuron syndrome due to cauda equina hypertrophy with onion bulbs

Erin K. O'Ferrall MD

Erin K. O'Ferrall MD

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

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Daniel Gendron MD

Daniel Gendron MD

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

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Marie-Christine Guiot MD

Marie-Christine Guiot MD

Department of Pathology, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

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Jeffery Hall MD

Jeffery Hall MD

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

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Michael Sinnreich MD, PhD

Corresponding Author

Michael Sinnreich MD, PhD

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

University Hospital Basel, Neuromuscular Center, Department of Neurology, University Hospital, Petersgraben 4, 4031 Basel, Switzerland

Correspondence to: M. Sinnreich; e-mail: [email protected]Search for more papers by this author
First published: 20 February 2013
Citations: 15

Dr. O'Ferrall was supported by a clinical fellowship grant from the Alberta Heritage Foundation for Medical Research and by a Talecris Fellowship at the Montreal Neurological Institute. Dr. Sinnreich was supported by grants from CIHR-ALS-MDAC, AFM, and FRSQ.

ABSTRACT

Introduction: Hypertrophy of the nerve roots of the cauda equina may occur with both acquired and inherited neuropathies. Although selective nerve root involvement of the sensory roots has been described and termed chronic inflammatory sensory polyradiculoneuropathy (CISP), selective involvement of the proximal motor roots has not been described. Methods: Clinical, electrophysiological, MRI, and pathological findings are reported. Results: Here, we report a patient with cauda equina hypertrophy presenting with a pure lower motor neuron syndrome without clinical or electrophysiological evidence of sensory fiber involvement. Bowel and bladder functions were spared. Nerve root biopsy demonstrated abundant onion bulb formations. The patient experienced improvement in motor function with immunomodulatory treatment. Conclusions: We suggest the term chronic immune demyelinating motor polyradiculopathy (CIMP) to describe this particular form of CIDP, thereby expanding the clinical spectrum of CIDP. Muscle Nerve, 48: 301–305, 2013

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