Polymyositis and the Spectrum of Scleroderma Disorders

Polymyositis (PM) is usually associated to other autoimmune or connective tissue diseases. The authors report the case of a 59-year-old man with pulmonary fibrosis, who presented with constitutional symptoms and gradually developed proximal muscle weakness, Raynaud phenomenon, and dysphagia. Besides...

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Main Authors: Joana Cochicho, João Madaleno, Emília Louro, Adélia Simão, Armando Carvalho
Format: Article
Language:English
Published: SMC MEDIA SRL 2015-12-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:http://ejcrim.com/index.php/EJCRIM/article/view/346
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author Joana Cochicho
João Madaleno
Emília Louro
Adélia Simão
Armando Carvalho
author_facet Joana Cochicho
João Madaleno
Emília Louro
Adélia Simão
Armando Carvalho
author_sort Joana Cochicho
collection DOAJ
description Polymyositis (PM) is usually associated to other autoimmune or connective tissue diseases. The authors report the case of a 59-year-old man with pulmonary fibrosis, who presented with constitutional symptoms and gradually developed proximal muscle weakness, Raynaud phenomenon, and dysphagia. Besides creatine kinase (CK) elevation, he had positive anti-Polymyositis-Scleromyositis (PM-Scl) and anti-Sjögren's-syndrome A (SSA) antibodies. Nailfold capillaroscopy showed a scleroderma pattern and muscle biopsy revealed necrosis, regeneration of muscle fibers, and inflammatory infiltrate. Prednisolone was started, with great improvement. Taking into account the overlap features between PM and systemic sclerosis sine scleroderma, it is important to closely monitor the patient for signs of pulmonary and cardiac decompensation.
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spelling doaj.art-603e9ed3969b467ba3628cb821cfbebb2022-12-22T00:37:04ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942015-12-013110.12890/2015_000346131Polymyositis and the Spectrum of Scleroderma DisordersJoana Cochicho0João Madaleno1Emília Louro2Adélia Simão3Armando Carvalho4Coimbra Hospital and Universitary CentreCoimbra Hospital and Universitary CentreCoimbra Hospital and Universitary CentreCoimbra Hospital and Universitary CentreCoimbra Hospital and Universitary CentrePolymyositis (PM) is usually associated to other autoimmune or connective tissue diseases. The authors report the case of a 59-year-old man with pulmonary fibrosis, who presented with constitutional symptoms and gradually developed proximal muscle weakness, Raynaud phenomenon, and dysphagia. Besides creatine kinase (CK) elevation, he had positive anti-Polymyositis-Scleromyositis (PM-Scl) and anti-Sjögren's-syndrome A (SSA) antibodies. Nailfold capillaroscopy showed a scleroderma pattern and muscle biopsy revealed necrosis, regeneration of muscle fibers, and inflammatory infiltrate. Prednisolone was started, with great improvement. Taking into account the overlap features between PM and systemic sclerosis sine scleroderma, it is important to closely monitor the patient for signs of pulmonary and cardiac decompensation.http://ejcrim.com/index.php/EJCRIM/article/view/346Polymyositis, Systemic sclerosis sine scleroderma, Overlap syndrome
spellingShingle Joana Cochicho
João Madaleno
Emília Louro
Adélia Simão
Armando Carvalho
Polymyositis and the Spectrum of Scleroderma Disorders
European Journal of Case Reports in Internal Medicine
Polymyositis, Systemic sclerosis sine scleroderma, Overlap syndrome
title Polymyositis and the Spectrum of Scleroderma Disorders
title_full Polymyositis and the Spectrum of Scleroderma Disorders
title_fullStr Polymyositis and the Spectrum of Scleroderma Disorders
title_full_unstemmed Polymyositis and the Spectrum of Scleroderma Disorders
title_short Polymyositis and the Spectrum of Scleroderma Disorders
title_sort polymyositis and the spectrum of scleroderma disorders
topic Polymyositis, Systemic sclerosis sine scleroderma, Overlap syndrome
url http://ejcrim.com/index.php/EJCRIM/article/view/346
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