Literature DB >> 11257161

Pulmonary involvement in juvenile dermatomyositis: a two-year longitudinal study.

S Trapani1, G Camiciottoli, A Vierucci, M Pistolesi, F Falcini.   

Abstract

OBJECTIVE: To investigate the prevalence and features of asymptomatic pulmonary involvement in juvenile dermatomyositis (JDM).
METHODS: Twelve JDM patients underwent pulmonary function tests at baseline, 12 and 24 months. Disease activity, duration, serum lactate dehydrogenase (LDH) values and antinuclear antibody (ANA) titres were also evaluated.
RESULTS: Five patients showed lung impairment at baseline and four at 12 and 24 months. Forced expiratory volume in 1s, forced vital capacity (FVC), carbon monoxide diffusing capacity (DLCO) and alveolar volume were the most frequently altered variables, indicating a restrictive pattern and impairment of diffusion. The prevalence and features of pulmonary alterations did not change during follow-up. FVC values were significantly lower in active JDM patients and were inversely related to LDH. DLCO values were significantly lower in ANA-positive patients. About half of the patients of this small case series of JDM had asymptomatic lung disease.
CONCLUSIONS: We suggest that lung function should be evaluated at disease onset and regularly during follow-up, as pulmonary function tests can detect otherwise unpredictable pulmonary involvement.

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Year:  2001        PMID: 11257161     DOI: 10.1093/rheumatology/40.2.216

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  6 in total

1.  Successful use of extracorporeal membrane oxygenation for severe interstitial lung disease in a child with dermatomyositis.

Authors:  Francesco Zulian; Maria Martha Martinez Toledo; Angela Amigoni; Giorgia Martini; Caterina Agosto; Andrea Pettenazzo
Journal:  Intensive Care Med       Date:  2007-06-27       Impact factor: 17.440

Review 2.  Rare Lung Diseases: Interstitial Lung Diseases and Lung Manifestations of Rheumatological Diseases.

Authors:  Mahesh Babu Ramamurthy; Daniel Y T Goh; Michael Teik Chung Lim
Journal:  Indian J Pediatr       Date:  2015-08-20       Impact factor: 1.967

3.  Assessment, classification and treatment of calcinosis as a complication of juvenile dermatomyositis: a survey of pediatric rheumatologists by the childhood arthritis and rheumatology research alliance (CARRA).

Authors:  A B Orandi; K W Baszis; V R Dharnidharka; A M Huber; M F Hoeltzel
Journal:  Pediatr Rheumatol Online J       Date:  2017-09-21       Impact factor: 3.054

Review 4.  Respiratory symptoms as initial manifestations of interstitial lung disease in clinically amyopathic juvenile dermatomyositis: a case report with literature review.

Authors:  Jingyi Xia; Gaoli Jiang; Tingting Jin; Quanli Shen; Yangyang Ma; Libo Wang; Liling Qian
Journal:  BMC Pediatr       Date:  2021-11-03       Impact factor: 2.125

Review 5.  Adult and juvenile dermatomyositis: are the distinct clinical features explained by our current understanding of serological subgroups and pathogenic mechanisms?

Authors:  Sarah L Tansley; Neil J McHugh; Lucy R Wedderburn
Journal:  Arthritis Res Ther       Date:  2013-04-08       Impact factor: 5.156

Review 6.  The Vasculopathy of Juvenile Dermatomyositis.

Authors:  Charalampia Papadopoulou; Liza J McCann
Journal:  Front Pediatr       Date:  2018-10-09       Impact factor: 3.418

  6 in total

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