Fatal interstitial pulmonary fibrosis in anti-Jo-1-negative amyopathic dermatomyositis

Whitney A. High; Jack B. Cohen; Bettina A. Murphy; Melissa I. Costner

doi:10.1067/S0190-9622(03)01482-8

Fatal interstitial pulmonary fibrosis in anti-Jo-1-negative amyopathic dermatomyositis

Whitney A. High, Jack B. Cohen, Bettina A. Murphy, Melissa I. Costner

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Abstract

Amyopathic dermatomyositis (DM) describes a subpopulation with the cutaneous eruption of DM, but without muscle involvement. Interstitial pulmonary fibrosis is a recognized complication of DM, often correlated with antisynthetase enzymes, such as anti-Jo-1. We describe a case of fatal IPF in a patient with anti-Jo-1 antibody-negative amyopathic DM.

Original language	English (US)
Pages (from-to)	295-298
Number of pages	4
Journal	Journal of the American Academy of Dermatology
Volume	49
Issue number	2
DOIs	https://doi.org/10.1067/S0190-9622(03)01482-8
State	Published - Aug 1 2003

ASJC Scopus subject areas

Dermatology

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10.1067/S0190-9622(03)01482-8

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title = "Fatal interstitial pulmonary fibrosis in anti-Jo-1-negative amyopathic dermatomyositis",

abstract = "Amyopathic dermatomyositis (DM) describes a subpopulation with the cutaneous eruption of DM, but without muscle involvement. Interstitial pulmonary fibrosis is a recognized complication of DM, often correlated with antisynthetase enzymes, such as anti-Jo-1. We describe a case of fatal IPF in a patient with anti-Jo-1 antibody-negative amyopathic DM.",

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AU - Costner, Melissa I.

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N2 - Amyopathic dermatomyositis (DM) describes a subpopulation with the cutaneous eruption of DM, but without muscle involvement. Interstitial pulmonary fibrosis is a recognized complication of DM, often correlated with antisynthetase enzymes, such as anti-Jo-1. We describe a case of fatal IPF in a patient with anti-Jo-1 antibody-negative amyopathic DM.

AB - Amyopathic dermatomyositis (DM) describes a subpopulation with the cutaneous eruption of DM, but without muscle involvement. Interstitial pulmonary fibrosis is a recognized complication of DM, often correlated with antisynthetase enzymes, such as anti-Jo-1. We describe a case of fatal IPF in a patient with anti-Jo-1 antibody-negative amyopathic DM.

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Fatal interstitial pulmonary fibrosis in anti-Jo-1-negative amyopathic dermatomyositis

Abstract

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