Summary
Multifocal central white matter axonal swelling characterized electron microscopically by focal axonal mitochondrial and membraneous body enrichment occurred in a 52 year old man who presented with the chief complaint of severe progressive muscular weakness accompanied by disorientation. The clinical and pathological findings in this patient appear unique and are presented in order to broaden our concepts of axis cylinder pathology.
References
Bove, K., Schwartz, D. C.: Focal lipid cardiomyopathy in an infant with paroxysmal atrial tachycardia. Arch. Path.95, 26–36 (1973)
Chou, S. M., Hartmann, H. A.: Axonal lesions and waltzing syndrome after IDPN administration in rats: With a concept-“axostasis”. Acta neuropath. (Berl.)3, 428–450 (1964)
Haese, W. H., Mason, B. J., Mirowski, M.: Peculiar focal myocardial degeneration and fatal arrhythmia in a child. New Engl. J. Med.287, 180–181 (1972)
Hallervorden, J., Spatz, H.: Eigenartige Erkrankung im extrapyramidalen System mit besonderer Beteiligung des Globus pallidus und der Substantia nigra. Z. ges. Neurol. Psychiat.79, 254–302 (1922)
Hedley-Whyte, T. E., Gelles, F. H., Uzman, B. G.: Infantile neuroaxonal dystrophy. A disease characterized by altered terminal axons and synaptic endings. Neurology (Minneap.)18, 891–906 (1968)
Herdson, P. G., Kaltenbach, J. P., Hennings, R. B.: Fine structural and biochemical changes in dog myocardium during autolysis. Amer. J. Path.57, 539–577 (1969)
Herman, M. M., Huttenlocher, P. R., Bensch, K. G.: Electron microscopic observations in infantile neuroaxonal dystrophy. Arch. Neurol. (Chic.)20, 19–34 (1969)
Jellinger, K.: Neuroaxonal dystrophy: Its natural history and related disorders. Progress in neuropathology, H. M. Zimmerman, ed. Vol. 2, pp. 129–180. New York. Grune & Stratton 1973
Kamoshita, S., Neustein, H. B., Landing, B. H.: Infantile neuroaxonal dystrophy with neonatal onset. Neuropathologic and electron microscopic observations. J. Neurophath. exp. Neurol.27, 300–323 (1968)
Kauffman, S. L., Chandra, N., Peress, N. S., Torres, R. R.: Idiopathic infantile cardiomyopathy with involvement of the conduction system. Amer. J. Cardiol.30, 648–652 (1972)
Koenig, H.: Acute axonal dystrophy caused by fluorocitrate: The role of mitochondrial swelling. Science164, 310–312 (1969)
Lampert, P., Blumberg, J. M., Pentschew, A.: An electron microscopic study of dystrophic axons in the gracile and cuneate nuclei of Vitamin E-deficient rats. J. Neuropath. exp. Neurol.23, 60–77 (1964)
Luft, R., Ikkos, D., Palmieri, G., Ernster, L., Afzelius, B.: A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: A correlated clinical, biochemical and morphological study. J. clin. Invest.41, 1776–1804 (1962)
Sandbank, U., Lerman, P., Gerfman, F.: Infantile neuroaxonal dystrophy: Cortical axonic and presynaptic changes. Acta neuropath. (Berl.)6, 164–174 (1966)
Seitelberger, F.: Eine unbekannte Form von infantiler Lipoidspeicherkrankheit des Gehirns. Proc. First Internat. Congr. Neuropath. (Rome, September 1952), Vol. 3, pp. 323–333. Turin: Rosenberg and Sellier 1952
Slagel, D. E., Hartman, H. A.: The distribution of neuroaxonal lesions in mice injected with iminodiproprionitrile with specific reference to the vestibular system. J. Neuropath. exp. Neurol.24, 599–620 (1965)
Sung, J. G.: Neuroaxonal dystrophy in aging. Proc. Fifth Int. Congr. Neuropath., pp. 478–480. New York: Excerpta Medica Foundation 1966
Thibault, J.: Neuroaxonal dystrophy. A case of non-pigmented type and protracted course. Acta neuropath. (Berl.)21, 232–238 (1972)
Torack, R. M., Hughes, C. P.: Neuroaxonal dystrophy in subacute dementia. Acta neuropath. (Berl.)22, 264–268 (1972)
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Peress, N.S., Kim, BH. Profound muscle weakness associated with axis cylinder ballooning. Acta Neuropathol 28, 87–92 (1974). https://doi.org/10.1007/BF00687522
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DOI: https://doi.org/10.1007/BF00687522