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Subacute Structural Myopathy Associated With Human Immunodeficiency Virus Infection
Michael F. Gonzales, MBBS, FRCPA;
Richard K. Olney, MD;
Yuen T. So, MD, PhD;
Claudia M. Greco, MD;
Barbara A. McQuinn, MD;
Robert G. Miller, MD;
Stephen J. DeArmond, MD, PhD
Arch Neurol. 1988;45(5):585-587.
Abstract
An unusual myopathy characterized by selective loss of thick filaments and widespread formation of rod bodies is described in two men, both seropositive for human immunodeficiency virus. We were unable to find any previous reports documenting this combination of morphological abnormalities, which we believe may be related to human immunodeficiency virus infection. Both patients responded to treatment: one, to steroid therapy; the other, to plasmapheresis.
Author Affiliations
From the Departments of Pathology (Drs Gonzales, Greco, and DeArmond) and Neurology (Drs Olney, So, McQuinn, and Miller), University of California at San Francisco; the Departments of Pathology (Dr Greco) and Neurology (Dr Miller), Children's Hospital of San Francisco; and the Department of Anatomical Pathology, Royal Melbourne Hospital (Dr Gonzales).
Footnotes
Accepted for publication Oct 18, 1987.
Presented, in part, at the 39th annual meeting of the American Academy of Neurology, New York, April 8, 1987.
Reprint requests to Department of Neurology, M-794, Box 0114, University of California at San Francisco, San Francisco, CA 94143 (Dr Olney).
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