DSpace Repository

A case of Amyopathic Dermatomyositis associated with Interstitial Pulmonary Disease

Show simple item record

dc.creator Tunc, S. E.
dc.creator Ugan, Y.
dc.creator Dogru, A.
dc.creator Sahin, M.
dc.creator Bayram, D.
dc.creator Ceyhan, A. M.
dc.date 2015-11-01T00:00:00Z
dc.date.accessioned 2021-12-03T11:20:05Z
dc.date.available 2021-12-03T11:20:05Z
dc.identifier 36ff6008-e04a-44dc-8f22-5257bc1412a6
dc.identifier 10.7417/ct.2015.1897
dc.identifier https://avesis.sdu.edu.tr/publication/details/36ff6008-e04a-44dc-8f22-5257bc1412a6/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/90886
dc.description Inflammatory myopathies are a heterogeneous group of diseases with unknown etiology characterized by inflammation of the skeletal muscles and proximal muscle weakness. Dermatomyositis (DM) is an idiopathic inflammatory myopathy with characteristic cutaneous findings such as heliotrope rash, Gottron's sign, Gottron's papules, shawl sign and machinist hand. Amyopathic dermatomyositis (ADM) is a rare but well-recognized clinical subtype of DM, constituting aproximately 10-20% of patients with this disease. It generally manifests only pathognomonic skin findings without clinical and laboratory evidence of muscle involvement. In this report, we present a rare case of ADM associated with interstitial pulmonary disease.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title A case of Amyopathic Dermatomyositis associated with Interstitial Pulmonary Disease
dc.type info:eu-repo/semantics/article


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account