Abstract
Thick round fibres common in cross sections of muscle biopsies from patients with muscular dystrophy are due to contracted and swollen segments of otherwise normal muscle fibres. This contracture leads to segmental fibre breakdown, which is identical with Zenker's waxy degeneration. In biopsies from 90 patients suspected of neuromuscular disease, segmental contracture was seen in all or nearly all patients with infantile muscular dystrophy, necrotic myopathy or acute alcoholic myopathy. It was present in half of the patients with polymyositis or myotonic dystrophy. In resticted forms of muscular dystrophy it was rare as it was in neurogenic atrophy. In 9 clinically normal patients it was absent. In electron micrographs of the initial stage sarcomeres were moderately shortened, the sarcoplasmic reticulum was distended and the mitochondria were normal. In the plasmalemma holes were found, through which glycogen granules were lost into the interstitial tissue. In later stages myofibrils were overcontracted and homogenized; in large areas the plasmalemma was absent. Based on these findings a hypothesis for the development of waxy degeneration is proposed: locally defects of the plasmamembrane cause segmental contracture, glycogen granules and water soluble enzymes are lost through holes in the plasma membrane, and finally the affected fibre segment becomes necrotic.
MeSH Terms
Adolescent
Adult
Aged
Basement Membrane/ultrastructure
Child
Child, Preschool
Female
Glycogen/analysis
Humans
Infant
Male
Middle Aged
Mitochondria, Muscle/ultrastructure
Muscle Contraction
Muscles/ultrastructure
Muscular Diseases/pathology
Muscular Dystrophies/pathology
Myofibrils/ultrastructure
Myotonic Dystrophy/pathology
Neuromuscular Diseases/pathology
Sarcolemma/ultrastructure
Sarcoplasmic Reticulum/ultrastructure
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schmalbruch H
References (15)
15 references, click to expand
-
Contracture knots in normal and diseased muscle fibres.
Brain. 1973 Sep;96(3):637-40
PMID: 4743937
-
Lipids of dystrophic and normal mouse muscle: whole tissue and particulate fractions.
J Lipid Res. 1970 Sep;11(5):486-95
PMID: 5501482
-
Studies in neuromuscular disease with radioactive potassium.
Neurology. 1953 Aug;3(8):604-8
PMID: 13087580
-
Abnormalities in membrane microviscosity and ion transport in genetic muscular dystrophy.
Nature. 1975 Apr 10;254(5500):525-6
PMID: 1121326
-
["Red" muscle fibres].
Z Zellforsch Mikrosk Anat. 1971;119(1):120-46
PMID: 4327534
-
Lipid changes in Duchenne muscular dystrophy.
J Neurol Neurosurg Psychiatry. 1972 Oct;35(5):658-63
PMID: 5084134
-
Stages in fibre breakdown in Duchenne muscular dystrophy. An electron-microscopic study.
J Neurol Sci. 1975 Feb;24(2):179-200
PMID: 163299
-
Structural difference between resting and rigor muscle; evidence from intensity changes in the lowangle equatorial x-ray diagram.
J Mol Biol. 1968 Nov 14;37(3):507-20
PMID: 5719221
-
Muscular dystrophy: cation concentrations in residual muscle.
J Appl Physiol. 1955 Jul;8(1):22-30
PMID: 13242486
-
Compensatory hypertrophy in the extensor digitorum longus muscle of the rat.
J Anat. 1973 Oct;116(Pt 1):57-65
PMID: 4777781
-
Structural changes in the early stages of Duchenne muscular dystrophy.
J Neurol Neurosurg Psychiatry. 1972 Aug;35(4):451-5
PMID: 4115002
-
A reliable staining method for semi-thin sections in experimental neurfanatomy.
Brain Res. 1968 Aug 26;10(2):120-6
PMID: 4176326
-
[Erythrocyte lipids in progressive muscular dystrophy].
Clin Chim Acta. 1973 Feb 12;43(3):333-41
PMID: 4690906
-
[ON THE EFFECT OF ALKALI- AND EARTH ALKALI-IONS (NA+, K+, LI+, MG2+, CA2+) ON SOME STRUCTURES IN THE DIAPHRAGM OF MICE].
Z Zellforsch Mikrosk Anat. 1964 Mar 5;62:246-78
PMID: 14185427
-
Refractory and irresponsive periods of muscle in progressive muscular dystrophy and paresis due to lower motor neuron involvement.
Neurology. 1959 Nov;9:747-56
PMID: 13821597