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"Myopathic" Changes in Chronically Denervated Muscle
DANIEL B. DRACHMAN, MD;
SEAN R. MURPHY, MB, MRCP;
MOOL P. NIGAM, MD;
JOHN R. HILLS, MD
Arch Neurol. 1967;16(1):14-24.
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NEUROMUSCULAR diseases are generally divided into two categories: the neuropathies and the myopathies. Neuropathic disorders are those in which motor nerve cells or their processes are first affected, resulting secondarily in atrophy of muscle. In the primary myopathies the disease process is assumed to involve the muscle directly, without damaging its nerve supply. Clinical, laboratory, and electromyographic findings are often useful in distinguishing between these two classes of disorders, but the muscle biopsy may be the deciding factor.
In general, interpretation of the muscle biopsy has been based on two principles: (1) Following denervation, muscle fibers belonging to the same motor unit undergo atrophy together and are located in groups. By contrast, myopathies attack individual muscle fibers at random, giving rise to scattered changes throughout the muscle. (2) In myopathic disorders architectural changes are found in medium-sized and larger muscle fibers. On the other hand, denervation leads to
. . . [Full Text PDF of this Article]
Author Affiliations
BOSTON
From the Department of Neurology, Tufts-New England Medical Center, Boston.
Footnotes
Submitted for publication Aug 2, 1966; accepted Aug 25.
Read in part before the 18th Annual Meeting of the American Academy of Neurology, Philadelphia, April 28, 1966.
Reprint requests to Department of Neurology, Tufts-New England Medical Center, Boston 02111 (Dr. Drachman).
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