Gastrointestinal Involvement in Inflammatory Myositis

M. Pérez-de-Lis Novo; R. Pérez-Álvarez; L. Pallarés-Ferreres; J. J. Fernández-Martín; M. J. Soto Cárdenas; A. Selva-O'Callaghan

doi:10.1016/B978-0-444-63707-9.00014-3

Gastrointestinal Involvement in Inflammatory Myositis

M. Pérez-de-Lis Novo, R. Pérez-Álvarez, L. Pallarés-Ferreres, J. J. Fernández-Martín, M. J. Soto Cárdenas, A. Selva-O'Callaghan

Department of Medicine

Research output: Chapter in Book › Chapter › Research › peer-review

Abstract

© 2017 Elsevier B.V. Inflammatory myopathies (IMs) are a group of rare immune-mediated diseases characterized by proximal muscle weakness and mononuclear cell inflammation of the skeletal muscle. IMs are the largest group of potentially treatable myopathies and form a heterogeneous group of disorders. We may classify them into five subtypes according to their clinicopathologic features: dermatomyositis, polymyositis, necrotizing autoimmune myositis, inclusion body myositis, and overlap myositis. The precise diagnosis of the subtype and the differential diagnosis from other diseases that have similar signs and symptoms are fundamental, as each subtype has a different prognosis and therapeutic response.

Original language	English
Title of host publication	Handbook of Systemic Autoimmune Diseases
Pages	263-270
Number of pages	7
Volume	13
DOIs	https://doi.org/10.1016/B978-0-444-63707-9.00014-3
Publication status	Published - 1 Jan 2017

Keywords

Dysphagia
Gastrointestinal vasculitis
Inflammatory bowel disease
Inflammatory myopathy
Pneumatosis intestinalis
Polymyositis

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title = "Gastrointestinal Involvement in Inflammatory Myositis",

abstract = "{\textcopyright} 2017 Elsevier B.V. Inflammatory myopathies (IMs) are a group of rare immune-mediated diseases characterized by proximal muscle weakness and mononuclear cell inflammation of the skeletal muscle. IMs are the largest group of potentially treatable myopathies and form a heterogeneous group of disorders. We may classify them into five subtypes according to their clinicopathologic features: dermatomyositis, polymyositis, necrotizing autoimmune myositis, inclusion body myositis, and overlap myositis. The precise diagnosis of the subtype and the differential diagnosis from other diseases that have similar signs and symptoms are fundamental, as each subtype has a different prognosis and therapeutic response.",

keywords = "Dysphagia, Gastrointestinal vasculitis, Inflammatory bowel disease, Inflammatory myopathy, Pneumatosis intestinalis, Polymyositis",

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AU - Pérez-de-Lis Novo, M.

AU - Pérez-Álvarez, R.

AU - Pallarés-Ferreres, L.

AU - Fernández-Martín, J. J.

AU - Soto Cárdenas, M. J.

AU - Selva-O'Callaghan, A.

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AB - © 2017 Elsevier B.V. Inflammatory myopathies (IMs) are a group of rare immune-mediated diseases characterized by proximal muscle weakness and mononuclear cell inflammation of the skeletal muscle. IMs are the largest group of potentially treatable myopathies and form a heterogeneous group of disorders. We may classify them into five subtypes according to their clinicopathologic features: dermatomyositis, polymyositis, necrotizing autoimmune myositis, inclusion body myositis, and overlap myositis. The precise diagnosis of the subtype and the differential diagnosis from other diseases that have similar signs and symptoms are fundamental, as each subtype has a different prognosis and therapeutic response.

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KW - Gastrointestinal vasculitis

KW - Inflammatory bowel disease

KW - Inflammatory myopathy

KW - Pneumatosis intestinalis

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