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      Answer to Alunno et al. “Different clinical presentations of primary Sjögren's syndrome: Not only a matter of age”. Joint Bone Spine 2021;88:105191

      , , , , ,
      Joint Bone Spine
      Elsevier BV

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          Interstitial lung disease in Sjögren's syndrome: a clinical review.

          Interstitial lung disease (ILD) is considered the most frequent and serious pulmonary complication in primary Sjögren's syndrome (pSS), with the majority of the studies indicating a prevalence of about 20%, and resulting in significant morbidity and mortality. Although ILD was historically described as a late manifestation of pSS, more recently, a high variability of the time of onset of pSS-ILD has been observed and from 10 to 51% of patients can develop ILD years before the onset of pSS. Lymphocytic interstitial pneumonia is highly typical for SS, but it occurs only in a few cases, while the most common ILD pattern is nonspecific interstitial pneumonia, followed by usual interstitial pneumonia and organising pneumonia. Multidisciplinary discussion can be necessary in pSS cases with ambiguous clinical findings, when differential diagnosis with IIPs might be very difficult. Up to date, available data do not allow to establish an evidence-based treatment strategy in pSS-ILD. Glucocorticoids are empirically used, usually in association to immunosuppressive drugs, such as cyclophosphamide and mycophenolate mofetil. A better understanding of the molecular mechanisms involved in the pathogenesis of pSS should facilitate the development of new therapies. Recently, a trial showed the efficacy of the antifibrotic drug nintedanib in slowing progression of various interstitial lung diseases, including patients with connective tissue diseases. The aims of this review are to describe clinical features, imaging, pathology, together with diagnostic criteria, prognosis and management of pSS-ILD patients.
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            Prevalence and risk factors of interstitial lung disease in patients with primary Sjögren's syndrome: A systematic review and meta-analysis.

            To systematically review the prevalence and risk factors for interstitial lung disease (ILD) in patients with primary Sjögren's syndrome (pSS).
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              Elderly-onset primary Sjögren's syndrome focused on clinical and salivary gland ultrasonographic features.

              To assess the clinical, laboratory, and salivary gland ultrasound (SGUS) characteristics of elderly-onset of primary Sjögren's syndrome (EopSS).
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                Author and article information

                Contributors
                Journal
                Joint Bone Spine
                Joint Bone Spine
                Elsevier BV
                1297319X
                July 2021
                July 2021
                : 88
                : 4
                : 105199
                Article
                10.1016/j.jbspin.2021.105199
                f054a4e6-180d-4222-8763-9d09aadadc17
                © 2021

                https://www.elsevier.com/tdm/userlicense/1.0/

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