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

Author:

Romão Vasco C,Talarico Rosaria,Scirè Carlo AlbertoORCID,Vieira Ana,Alexander TobiasORCID,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

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.

Publisher

BMJ

Subject

Immunology,Immunology and Allergy,Rheumatology

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