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Clinicopathologic Characteristics of Polymyositis Patients with Numerous Tissue Eosinophils

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Specialty Neurology
Date 1996 Aug 1
PMID 8891055
Citations 2
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Abstract

Introduction: We evaluated associated clinicopathologic features of polymyositis (PM) patients with numerous tissue eosinophils.

Materials And Methods: 680 muscle biopsies were examined in our institution and eight were identified with greater than 0.3 eosinophils per square millimeter in the inflammatory infiltrate without concomitant peripheral eosinophilia.

Results: All eight patients had typical PM, but neither dermatomyositis nor inclusion body myositis was identified. Clinically, a large number of PM patients with eosinophils manifested an acute- or subacute-onset of symptoms, myoglobinuria, a marked elevation of serum creatine kinase, a good response to steroid therapy, and a relatively benign course compared with 26 PM patients without eosinophils. Muscle biopsies demonstrated necrotic fibers more frequently in PM patients with eosinophils than in PM patients without eosinophils. Hypertrophic fibers, fiber splitting, basophilic fibers, and lobulated fibers were less frequently observed in PM patients with eosinophils.

Conclusion: These results suggest that the majority of PM patients with eosinophils may be steroid-responsive and suffer an acute or subacute onset of PM.

Citing Articles

The Immune Response and the Pathogenesis of Idiopathic Inflammatory Myositis: a Critical Review.

Ceribelli A, De Santis M, Isailovic N, Gershwin M, Selmi C Clin Rev Allergy Immunol. 2016; 52(1):58-70.

PMID: 26780034 DOI: 10.1007/s12016-016-8527-x.


Eosinophils in hereditary and inflammatory myopathies.

Schroder T, Fuchss J, Schneider I, Stoltenburg-Didinger G, Hanisch F Acta Myol. 2014; 32(3):148-53.

PMID: 24803842 PMC: 4006278.