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Submitted: 10 Apr 2022
Accepted: 24 May 2022
ePublished: 31 May 2022
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Immunopathol Persa. Inpress.
doi: 10.34172/ipp.2022.32406
  Abstract View: 1125

Case Report

First report of an adult patient with clinical amyopathic dermatomyositis associated rapid progressive interstitial lung disease triggered by COVID-19

Aida Varghaei 1 ORCID logo, Hengameh Mojdeganlou 2 ORCID logo, Masomeh Rabieepour 3 ORCID logo, Amir Mikaeilvand 4 ORCID logo, Ata Abbasi 5,2* ORCID logo

1 Department of Dermatology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
2 Department of Pathology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
3 Department of Internal Medicine, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
4 Department of Cardiology, Faculty of Medicine, Urmia University of Medical Science, Urmia, Iran
5 Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran
*Corresponding Author: Correspondence to Ata Abbasi, Email: , Email: aabbasi@alumnus.tums.ac.ir

Abstract

Interstitial lung disease (ILD) is a common manifestation of dermatomyositis (DM) with indolent course but a unique variant of DM called clinically amyopathic DM (CADM) presents with rapid progressive ILD (RP-ILD) and is called CADM associated RP-ILD. Here, we report a case of a 52-year-old woman with CADM associated RP-ILD occurred 2 weeks after recovery from COVID-19 infection but unfortunately died from RP-ILD, almost 5 months later. This is the first report of CADM associated RP-ILD triggered by COVID-19 in an adult patient.

Citation: Varghaei A, Mojdeganlou H, Rabieepour M, Mikaeilvand A, Abbasi A. First report of an adult patient with clinical amyopathic dermatomyositis associated rapid progressive interstitial lung disease triggered by COVID-19. Immunopathol Persa. 2022;x(x):e32406. DOI:10.34172/ ipp.2022.32406.
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