Primary Sjogren′s Syndrome presenting with Interstitial lung disease and Myositis

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منابع مشابه

Interstitial lung disease in antisynthetase syndrome without clinical myositis.

To cite: Sundaragiri PR, Vallabhajosyula S, Kanaan JP. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2014204296 DESCRIPTION Antisynthetase syndrome (ASS) is a lesser recognised idiopathic inflammatory myopathy with nearly 89% showing interstitial lung disease (ILD). However, in a small subpopulation without evidence of myositis, the diagnosis may be critically d...

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Interstitial lung disease in myositis: clinical subsets, biomarkers, and treatment.

Interstitial lung disease (ILD) is the most frequent organ involvement (found in nearly half) of myositis patients, but it reveals various clinical courses and therapeutic responsiveness according to clinical and serological subsets. Autoantibodies, as well as imaging and histopathological studies, are useful for the classification of ILD in myositis and provide useful information for predictin...

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Anti Jo-1 myositis. 'Mechanic's hands' and interstitial lung disease.

We report three patients who presented with painful weak muscles, a violaccous rash on the extensor aspect of their hands, elevated muscle enzymes, electromyographic and muscle biopsy findings typical ofpolymyositis. All three patients had anti JoI autoantibodies, 'mechanic's hands' and evidence of interstitial lung disease on CT scan. An incomplete response to corticosteroids was observed in a...

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Prognostic Factors for Myositis-Associated Interstitial Lung Disease

BACKGROUND Interstitial lung disease (ILD) is a common manifestation of polymyositis (PM), dermatomyositis (DM), and clinically amyopathic dermatomyositis (CADM); however, little is known about the factors influencing the prognosis for PM/DM/CADM-associated ILD. (PM/DM/CADM-ILD). The aim of the present study is to assess prognostic factors for PM/DM/CADM-ILD. METHODS The clinical features and...

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Primary Sjogrens Syndrome in a Child

Sjögren syndrome is uncommon in children and occurs most often in association with autoimmune diseases (secondary Sjögren syndrome). We describe the clinical and biological features of a 7-year-old girl with primary Sjögren syndrome revealed by recurrent parotiditis. CASE REPORT A 7-year-old girl was referred for investigation of multiple episodes of parotid swelling since age 4 years, withou...

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ژورنال

عنوان ژورنال: Muller Journal of Medical Sciences and Research

سال: 2014

ISSN: 0975-9727

DOI: 10.4103/0975-9727.135771