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Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis

Dermatomyositis (DM) is an autoimmune disease that is characterized by involvement of proximal musculature and skin. We report a 52-year-old woman with a 6-year history of dermatomyositis sine myositis, who developed lower extremity edema and proteinuria. Pathological examination of renal biopsy sho...

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Autores principales: Owlia, Mohammad Bagher, Hemayati, Roya, Taghipour Zahir, Shokouh, Moeini Nodeh, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424642/
https://www.ncbi.nlm.nih.gov/pubmed/22937456
http://dx.doi.org/10.1155/2012/751683
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author Owlia, Mohammad Bagher
Hemayati, Roya
Taghipour Zahir, Shokouh
Moeini Nodeh, Mohammad
author_facet Owlia, Mohammad Bagher
Hemayati, Roya
Taghipour Zahir, Shokouh
Moeini Nodeh, Mohammad
author_sort Owlia, Mohammad Bagher
collection PubMed
description Dermatomyositis (DM) is an autoimmune disease that is characterized by involvement of proximal musculature and skin. We report a 52-year-old woman with a 6-year history of dermatomyositis sine myositis, who developed lower extremity edema and proteinuria. Pathological examination of renal biopsy showed membranoproliferative glomerulonephritis. She received steroid, cyclophosphamide, and mycophenolate mofetil. Over the 9 to 10 months after the beginning of treatment, the proteinuria was improved.
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spelling pubmed-34246422012-08-30 Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis Owlia, Mohammad Bagher Hemayati, Roya Taghipour Zahir, Shokouh Moeini Nodeh, Mohammad Case Rep Rheumatol Case Report Dermatomyositis (DM) is an autoimmune disease that is characterized by involvement of proximal musculature and skin. We report a 52-year-old woman with a 6-year history of dermatomyositis sine myositis, who developed lower extremity edema and proteinuria. Pathological examination of renal biopsy showed membranoproliferative glomerulonephritis. She received steroid, cyclophosphamide, and mycophenolate mofetil. Over the 9 to 10 months after the beginning of treatment, the proteinuria was improved. Hindawi Publishing Corporation 2012 2012-08-13 /pmc/articles/PMC3424642/ /pubmed/22937456 http://dx.doi.org/10.1155/2012/751683 Text en Copyright © 2012 Mohammad Bagher Owlia et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Owlia, Mohammad Bagher
Hemayati, Roya
Taghipour Zahir, Shokouh
Moeini Nodeh, Mohammad
Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title_full Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title_fullStr Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title_full_unstemmed Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title_short Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis
title_sort dermatomyositis sine myositis with membranoproliferative glomerulonephritis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424642/
https://www.ncbi.nlm.nih.gov/pubmed/22937456
http://dx.doi.org/10.1155/2012/751683
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