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Article
October 1994

Dysautonomia With Acute Sensory Motor NeuropathyA New Classification of Acute Autonomic Neuropathy

Author Affiliations

From the Department of Neurology, Tokyo (Japan) Metropolitan Neurological Hospital (Drs Yokota, Hayashi, Hirashima, and Tanabe); and the Department of Neurology, Tokyo Medical and Dental University (Drs Yokota, Mitani, and Tsukagoshi).

Arch Neurol. 1994;51(10):1022-1031. doi:10.1001/archneur.1994.00540220068016
Abstract

Objectives:  To characterize the dysautonomia associated with acute sensory motor neuropathy and to discuss the classification of acute autonomic neuropathy.

Design:  Case series.

Methods:  Sympathetic skin response. Local sweat response to acetylcholine. Norepinephrine infusion test and acetylcholinesterase histochemistry of sural nerve biopsy specimens in addition to making conventional analyses of myelinated and unmyelinated fibers.

Results:  In 12 patients with chronic neuropathy, acetylcholinesterase-positive fiber density and plantar sympathetic skin response size were well correlated, but in the two patients with acute autonomic sensory and motor neuropathy, there were discrepancies, acetylcholinesterase-positive fiber density being well preserved and sympathetic skin responses being absent. Histologic and electrophysiologic results indicated primary demyelination of the myelinated fibers. In contrast, previous studies of acute autonomic sensory and motor neuropathy reported dysfunction of the sympathetic postganglionic fibers and axonopathic change in myelinated fibers, poor recovery from dysautonomia.

Conclusions:  Dysautonomia with acute idiopathic neuropathy can be divided into two categories—postganglionic axonopathic and preganglionic demyelinating types of the sympathetic efferent pathways. The recovery from dysautonomia produced by the former lesion is poor, but recovery is better for that produced by the latter lesion.

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