Benign monomelic amyotrophy of lower limb: report of three cases.

Abstract:

:Three patients with wasting confined to a single lower limb are reported. The characteristic features were: sporadic occurrence, insidious onset with slow progression and in 2 cases arrested course for at least 4 years, wasting out of proportion with disability, absence of sensory, pyramidal tract or bulbar signs. CK, motor and sensory conductions, and lumbar MRI were normal. Muscle CT showed selective loss of muscle tissue and fat replacement in posterior leg muscles. Quantitative electromyography and histologic findings revealed neurogenic features not only in the affected legs, but also in clinically uninvolved limbs. Monomelic amyotrophy of lower limb is a variant of spinal muscular atrophy with a benign course. However, as in the early stages of the disease there are no distinctive clinical or laboratory findings with other motor neuron diseases, the diagnosis of monomelic amyotrophy may be made only retrospectively after a prolonged observation.

journal_name

Acta Neurol Scand

authors

Uncini A,Servidei S,Delli Pizzi C,Cutarella R,Di Muzio A,Gambi D,Tonali P

doi

10.1111/j.1600-0404.1992.tb06035.x

subject

Has Abstract

pub_date

1992-06-01 00:00:00

pages

397-400

issue

6

eissn

0001-6314

issn

1600-0404

journal_volume

85

pub_type

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