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Inclusion Body Myositis Associated with Systemic Sarcoidosis

Published online by Cambridge University Press:  18 September 2015

Moris J. Danon ,
Osvaldo H. Perurena ,
Salve Ronan  and
Jose R. Manaligod
Moris J. Danon*
Affiliation:
Department of Neurology, University of Illinois College of Medicine, Chicago, Illinois Department of Pathology, University of Illinois College of Medicine, Chicago, Illinois
Osvaldo H. Perurena
Affiliation:
Department of Neurology, University of Illinois College of Medicine, Chicago, Illinois
Salve Ronan
Affiliation:
Department of Pathology, University of Illinois College of Medicine, Chicago, Illinois
Jose R. Manaligod
Affiliation:
Department of Pathology, University of Illinois College of Medicine, Chicago, Illinois
*
Department of Neurology, University of Illinois College of Medicine, 912 South Wood Street, Chicago, Illinois U.S.A. 60612
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Abstract:

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We report an autopsy study of a 64-year-old female with systemic sarcoidosis. In addition many muscles showed typical light and electron microscopic features of inclusion body myositis. To our knowledge this association has not been previously reported.

Type
Original Articles
Information
Canadian Journal of Neurological Sciences , Volume 13 , Issue 4 , November 1986 , pp. 334 - 336
Copyright
Copyright © Canadian Neurological Sciences Federation 1986

References

1.Carpenter, S, Karpati, G, Heller, I, et al. Inclusion body myositis: A distinct variety of idiopathic inflammatory myopathy. Neurology 1978; 28: 8–17.CrossRefGoogle ScholarPubMed
2.Danon, M, Reyes, M, Perurena, O, et al. Inclusion body myositis. A corticosteroid-resistant idiopathic inflammatory myopathy. Arch Neurol 1982; 39: 760–764.CrossRefGoogle ScholarPubMed
3.Lane, RAM, Fulthrope, SJ, Hudgson, P.Inclusion body myositis. A case with associated collagen vascular disease responding to treatment. J Neurol Neurosurg Psychiat 1985; 48: 270–273.CrossRefGoogle ScholarPubMed
4.Chad, D, Good, P, Adelman, L, et al. Inclusion body myositis associated with Sjogren’s syndrome. Arch Neurol 1982; 39: 186–188.CrossRefGoogle ScholarPubMed
5.Salama, J, Tomé, FMS, Lebon, P, et al. Myosite à inclusions. Étude clinique, morphologique et virologique concernant une nouvelle observation associée à une sclérodermie généralisée et à un syndrome de Klinefelter. Rev Neurol (Paris) 1980; 136: 863–878.Google Scholar
6.Riggs, J, Schochet, S, Gutmann, L, et al. Inclusion body myositis and chronic immune thrombocytopenia. Arch Neurol 1984; 41: 93–95.CrossRefGoogle ScholarPubMed
7.Gutmann, L, Govindan, S, Riggs, JE, et al. Inclusion body myositis and Sjogren’s syndrome. Arch Neurol 1985; 42: 1021–1022.CrossRefGoogle ScholarPubMed
8.Delaney, PN.Neurologic manifestations in sarcoidosis. Review of literature, with report of 23 cases. Annlnt Med 1977; 87: 336–345.Google ScholarPubMed
9.Namba, T, Brunnen, NG, Grob, D.Idiopathic giant cell polymyositis. Report of a case and review of the syndrome. Arch Neurol 1974; 31: 27–30.CrossRefGoogle ScholarPubMed
10.Itoh, J, Akiguichi, I, Reiko, M, et al. Sarcoid myopathy with typical rash of dermatomyositis. Neurology 1980; 30: 1118–1121.CrossRefGoogle ScholarPubMed
11.Eisen, A, Berry, K, Gibson, G.Inclusion body myositis: Myopathy or neuropathy. Neurology 1983; 33: 1109–1114.CrossRefGoogle ScholarPubMed
12.Smith, WT, Chad, D.Intranuclear inclusions in oculopharyngeal dystrophy. Muscle Nerve 1984; 7: 339–340.Google ScholarPubMed
13.Argov, Z, Yarom, R.“Rimmed vacuole myopathy” sparring the quadriceps. A unique disorder in Iranian Jews. J Neurol Sci 1984; 64: 33–43.CrossRefGoogle Scholar
14.Tateishi, J, Nagara, H, Ohta, M, et al. Intranuclear inclusions in muscle, nervous tissue and adrenal gland. Acta Neuropathol 1984; 63: 24–32.CrossRefGoogle ScholarPubMed
15.Kelly, JJ, Madoc-Jones, J, Adelman, LR, et al. Treatment of refractory polymyositis with total body irradiation. Neurology 1984; 34 (Suppl.): 80.Google Scholar
16.Mikol, J, Felten-Papaiconomou, A, Ferchal, F, et al. Inclusion body myositis: Clinicopathological studies and isolation of an adenovirus Type 2 from muscle biopsy specimen. Ann Neurol 1982; 11: 576–581.CrossRefGoogle ScholarPubMed
17.Chou, SM, Mizuno, Y.Mumps virus antigen in inclusion body myositis (IBM). Neurology 1985; 35 (Suppl.): 204.Google Scholar
18.James, DG, Neville, E, Walker, A.Immunology of sarcoidosis. Am J Med 1975; 59: 388–394.CrossRefGoogle ScholarPubMed
19.Hedfords, E.Clinical Immunology, Parker, C (ed.), WB Saunders 1; 1980, pp. 556–582.Google Scholar
20.Arahta, K, Engel, A.Monoclonal antibody analysis of mononuclear cells in myopathies. I: Quantitation of subsets according to diagnosis and sites of accumulation and demonstration and counts of muscle fibres invaded by T cells. Ann Neurol 1984; 16: 193–208.CrossRefGoogle Scholar
21.Engel, A, Arahata, K.Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes of auto-invasive cells in polymyositis and inclusion body myositis. Ann Neurol 1984; 16: 209–215.CrossRefGoogle ScholarPubMed