Publication:
A case of Hypomyopathic Dermatomyositis which subsequently developed to overt Myositis with ILD

creativeworkseries.issnISSN 2822-1893 eISSN 2822-2016
dc.contributor.authorSharma, Prayush
dc.contributor.authorDatta, Abhijit
dc.contributor.authorHossain, Mohammed Zakir
dc.date.accessioned2026-02-03T05:49:08Z
dc.date.available2026-02-03T05:49:08Z
dc.date.issued2022
dc.descriptionPrayush Sharma KIST Medical College and Teaching Hospital, Imadole Abhijit Datta Bangabandhu Sheikh Mujib Medical College Hospital, Faridpur, Bangladesh Mohammed Zakir Hossain Cumilla Medical College Hospital, Cumilla, Bangladesh
dc.description.abstractAbstract: Dermatomyositis (DM) is an inflammatory myositis. Clinically amyopathic dermatomyositis (CADM) and hypomyopathic dermatomyositis (HDM) are rare forms of DM in which skin manifestations are present with no and minimal clinical and laboratory evidence of myositis respectively. A common complication of CADM/HDM is interstitial lung disease (ILD), with the most common histopathologic variant of non-specific interstitial pneumonia (NSIP). This case highlights the development of ILD and severe muscle weakness, including proximal limb muscles, muscles of respiration and muscles of deglutition in a patient with previous diagnosis of hypomyopathic dermatomyositis.
dc.identifierhttps://doi.org/10.3126/nrj.v1i2.54905
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4471
dc.language.isoen_US
dc.publisherNepalese Respiratory Society
dc.subjectClinically Amyopathic Dermatomyositis (CADM)
dc.subjectDermatomyositis (DM)
dc.subjectHypomyopathic Dermatomyositis (HDM)
dc.subjectInterstitial Lung Disease (ILD)
dc.subjectNon-specific Interstitial Pneumonia
dc.titleA case of Hypomyopathic Dermatomyositis which subsequently developed to overt Myositis with ILD
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage27
oaire.citation.startPage25
relation.isJournalIssueOfPublication706d40d9-1a6a-4991-aaa1-3bb34da9ed66
relation.isJournalIssueOfPublication.latestForDiscovery706d40d9-1a6a-4991-aaa1-3bb34da9ed66
relation.isJournalOfPublication91ea7cc8-46b2-4796-94bd-2998c28b5ebb

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