Sjögren'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.

Sjögren's syndrome: state of the art on clinical practice guidelines / Romão, Vasco C; Talarico, Rosaria; Scirè, Carlo Alberto; Vieira, Ana; Alexander, Tobias; Baldini, Chiara; Gottenberg, Jacques-Eric; Gruner, Heidi; Hachulla, Eric; Mouthon, Luc; Orlandi, Martina; Pamfil, Cristina; Pineton de Chambrun, Marc; Taglietti, Marco; Toplak, Natasa; van Daele, Paul; van Laar, Jacob M; Bombardieri, Stefano; Schneider, Matthias; Smith, Vanessa; Cutolo, Maurizio; Mosca, Marta; Mariette, Xavier. - In: RMD OPEN. - ISSN 2056-5933. - 4:Suppl 1(2018), pp. N/A-N/A. [10.1136/rmdopen-2018-000789]

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

ORLANDI, MARTINA;
2018

Abstract

Sjögren'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.
2018
4
Suppl 1
N/A
N/A
Sjögren's syndrome: state of the art on clinical practice guidelines / Romão, Vasco C; Talarico, Rosaria; Scirè, Carlo Alberto; Vieira, Ana; Alexander, Tobias; Baldini, Chiara; Gottenberg, Jacques-Eric; Gruner, Heidi; Hachulla, Eric; Mouthon, Luc; Orlandi, Martina; Pamfil, Cristina; Pineton de Chambrun, Marc; Taglietti, Marco; Toplak, Natasa; van Daele, Paul; van Laar, Jacob M; Bombardieri, Stefano; Schneider, Matthias; Smith, Vanessa; Cutolo, Maurizio; Mosca, Marta; Mariette, Xavier. - In: RMD OPEN. - ISSN 2056-5933. - 4:Suppl 1(2018), pp. N/A-N/A. [10.1136/rmdopen-2018-000789]
Romão, Vasco C; Talarico, Rosaria; Scirè, Carlo Alberto; Vieira, Ana; Alexander, Tobias; Baldini, Chiara; Gottenberg, Jacques-Eric; Gruner, Heidi; Hachulla, Eric; Mouthon, Luc; Orlandi, Martina; Pamfil, Cristina; Pineton de Chambrun, Marc; Taglietti, Marco; Toplak, Natasa; van Daele, Paul; van Laar, Jacob M; Bombardieri, Stefano; Schneider, Matthias; Smith, Vanessa; Cutolo, Maurizio; Mosca, Marta; Mariette, Xavier
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1318504
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