File:Nervous and mental diseases (1911) (14775178011).jpg

Identifier: nervousmentald00chur (find matches)
Title: Nervous and mental diseases
Year: 1911 (1910s)
Authors: Church, Archibald, b. 1861 Peterson, Frederick, 1859-1938, joint author
Subjects: Nervous system
Publisher: Philadelphia and London, W. B. Saunders company
Contributing Library: The Library of Congress
Digitizing Sponsor: The Library of Congress

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emotor and trophic portions of the central apparatus, and constitutes aprimordial shortcoming bv which these parts reach an earlv death. 26 402 DISEASES OF THE CORD PROPER. Morbid Anatomy.—The lesions of progressive spinal muscularatrophy embrace in rare cases the entire motor field of the nervousapparatus from cerebral cortex to muscular nerve-endings, and includethe muscles themselves. Both upper and lower motor neurons in theirentirety are destroyed by a degenerative process. Following the patholog-ical rule that a neuron degenerating from toxic cause or involution firstshows changes in its peripheral portion, the upper motor segment maypresent alteration only in the pyramidal fibers of the cord. This mayreach the medulla, and, as a rule, does not extend into the peduncles,capsule, and cortex, though it may do so. In the lower neuron the de-generation is probably at first peripheral, but in all cases that reach amarked development the cells of the anterior gray are found degener-
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Fig. 155.—Cord-sections in a case of amyotrophic lateral sclerosis. 1, Lumbar region; 2, dorsal region; 3, cervical region (Marie). ated. Attending this we have muscular atrophy, with fibroid and fattychanges and degeneration in the motor fibers of the nerve-trunks, limitedsharply by the anatomical relations of the diseased cord-elements. In the cord the gray substance of the anterior horns shows atrophy.The ganglion-cells, many of which usually have disappeared, are wastedand degenerated, and there is a general shrinking of all the nervous ele-ments of the horn. The white substance of both the direct and crossedpyramidal tracts shows sclerotic degeneration. This process is notstrictly confined to them, but usually involves the anterolateral tracts toa lesser degree, and may invade the lateral limiting layer. This is espe-cially the case in the upper dorsal and cervical regions. The columnsof Groll sometimes show slight changes, apparently due to the shrinkingof the myelin, and not

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