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Extraocular muscle biopsy in chronic progressive external ophthalmoplegia
Author(s) -
Ringel Steven P.,
Bruce W. Wilson,
Barden Michael T.
Publication year - 1979
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410060406
Subject(s) - extraocular muscles , muscle biopsy , reinnervation , medicine , biopsy , anatomy , pathology , chronic progressive external ophthalmoplegia , myopathy , external ophthalmoplegia , mitochondrial myopathy , biology , biochemistry , gene , mitochondrial dna
Abstract A quantitative assessment of the pathological changes in extraocular muscle is presented in 8 patients with chronic progressive external ophthalmoplegia (CPEO). Serial cross‐sections of extraocular muscle were stained with a battery of histochemical and immunohistochemical techniques and compared with 36 normal extraocular muscles and 1 muscle from a patient who had longstanding third nerve palsy with anomalous reinnervation. Several of the patient had a striking increase in the number of ragged‐red fibers in extraocular muscle, particularly if frequent ragged‐red fibers also were found on limb muscle biopsy. One patient demonstrated extrajunctional acetylcholine receptor (AChR) in a small percentage of fibers, although this finding was not present in the reinnervated muscle. Numerous darkly staining central regions were noted in the ocular muscle fibers of a patient with Stephens syndrome (CPEO, peripheral neuropathy, and cerebellar disease) and in the reinnervated muscle. A patient with myotubular myopathy had single central nuclei in both limb and ocular muscle. All patients demonstrated in their extraocular muscles variation in both the size and distribution of each of the three histochemical fiber types. Extraocular muscule biopsy proved to be a safe, reliable technique. As a similar quantitative analysis is applied to the study of further patients, a better understanding of the pathogenesis of CPEO should be possible.