Sjogren's syndrome: state of the art on clinical practice guidelines - Archive ouverte HAL
Article Dans Une Revue RMD Open : Rheumatic & Musculoskeletal Diseases Année : 2018

Sjogren's syndrome: state of the art on clinical practice guidelines

1 CHULN - Centro Hospitalar Universitário Lisboa Norte [Lisbon, Portugal]
2 Azienda Ospedaliera Universitaria Pisana
3 UniFE - Università degli Studi di Ferrara = University of Ferrara
4 LPCDR - Liga Portuguesa Contra as Doenças Reumaticas
5 Charité - UniversitätsMedizin = Berlin University Medicine
6 UniPi - University of Pisa [Italy] = Università di Pisa [Italia] = Université de Pise [Italie]
7 I2CT - Immunologie, Immunopathologie et Chimie Thérapeutique
8 ICT - Immunopathologie et chimie thérapeutique
9 HUS - Les Hôpitaux Universitaires de Strasbourg
10 Centro Hospitalar de Lisboa Central E.P.E
11 INFINITE - Institute for Translational Research in Inflammation - U 1286
12 CHRU Lille - Centre Hospitalier Régional Universitaire [CHU Lille]
13 Hôpital Cochin [AP-HP]
14 UPD5 - Université Paris Descartes - Paris 5
15 UniFI - Università degli Studi di Firenze = University of Florence = Université de Florence
16 CHU Pitié-Salpêtrière [AP-HP]
17 SU - Sorbonne Université
18 Azienda Socio Sanitaria Territoriale Spedali Civili di Brescia [Brescia]
19 UMCL - University Medical Centre Ljubljana [Ljubljana, Slovenia]
20 Erasmus MC - Erasmus University Medical Center [Rotterdam]
21 Universiteit Utrecht / Utrecht University [Utrecht]
22 University Hospital Düsseldorf
23 Ghent University Hospital
24 UniGe - Università degli studi di Genova = University of Genoa
25 IMVA - U1184 - Immunologie des Maladies Virales et Autoimmunes
26 HUPS - Hôpitaux Universitaires Paris Sud [AP-HP]
Cristina Pamfil
  • Fonction : Auteur

Résumé

Sjogren's syndrome (SS) is a complex autoimmune rheumatic disease that specifically targets salivary and lachrymal glands. As such, patients typically had ocular and oral dryness and salivary gland swelling. Moreover, skin, nasal and vaginal dryness are frequently present. In addition to dryness, musculoskeletal pain and fatigue are the hallmarks of this disease and constitute the classic symptom triad presented by the vast majority of patients. Up to 30% to 50 % of patients with SS may present systemic disease; moreover, there is an increased risk for the development of non-Hodgkin's lymphoma that occurs in a minority of patients. The present work was developed in the framework of the European Reference Network (ERN) dedicated to Rare and Complex Connective Tissue and Musculoskeletal Diseases (ReCONNET). In line with its goals of aiming to improve early diagnosis, treatment and care of rare connective and musculoskeletal diseases, ERN-ReCONNET set to review the current state of clinical practice guidelines (CPGs) in the rare and complex connective tissue diseases of interest of the network. Therefore, the present work was aimed at providing a state of the art of CPGs for SS.
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Dates et versions

hal-03955282 , version 2 (24-01-2023)
hal-03955282 , version 1 (19-04-2023)

Identifiants

Citer

Vasco C. Romão, Rosaria Talarico, Carlo Alberto Scirè, Ana Vieira, Tobias Alexander, et al.. Sjogren's syndrome: state of the art on clinical practice guidelines. RMD Open : Rheumatic & Musculoskeletal Diseases, 2018, 4 (Suppl 1), pp.e000789. ⟨10.1136/rmdopen-2018-000789⟩. ⟨hal-03955282v2⟩
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