Volume 55, Issue 6 pp. 858-861
Clinical Research

Lesion distribution among 281 patients with sporadic neuralgic amyotrophy

Mark A. Ferrante MD

Corresponding Author

Mark A. Ferrante MD

Department of Neurology, University of Tennessee Health Science Center, Memphis, Tennessee, USA

Correspondence to: M. A. Ferrante, 6614 Heronswood Cove, Memphis, TN 38119; E-mail: [email protected]Search for more papers by this author
Asa J. Wilbourn MD

Asa J. Wilbourn MD

Cleveland Clinic Foundation, Cleveland, Ohio, USA

Search for more papers by this author
First published: 28 September 2016
Citations: 69

Conflicts of Interest: The authors have nothing to disclose.

ABSTRACT

Introduction

The muscles commonly affected by neuralgic amyotrophy (NA) are well known, but the location of the responsible lesions is less clear (plexus versus extraplexus).

Methods

We report the lesion locations in 281 NA patients as determined by extensive electrodiagnostic (EDX) testing.

Results

Our 281 patients had 322 bouts of NA, 57 of which were bilateral, for a total of 379 assessable events. A single nerve was involved in 174 (46%), and 205 (54%) were multifocal. EDX testing identified 703 individual lesions: 699 neuropathies and 4 supraclavicular radiculoplexus lesions.

Conclusions

The frequency of nerve involvement reflects the motor predilection of NA. Involvement of pure motor nerves exceeded that of predominantly motor nerves, both of which far exceeded involvement of more evenly mixed sensorimotor nerves. Cutaneous sensory nerves were least commonly involved. Because of the common C5–C6 innervation, NA often mimics an upper plexus lesion. Extraplexus nerve involvement far exceeded plexus involvement. Distal motor branch involvement explains the severe single-muscle wasting and weakness often observed. Muscle Nerve 55: 858–861, 2017

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