Behcet’s syndrome (BS) is a vasculitis, seen more commonly around the Mediterranean
and the Far East, and manifests with oral and genital ulcerations, skin lesions, uveitis, and …

Pseudo-pseudo Meigs’ syndrome (PPMS) is a rare manifestation of patients with systemic
lupus erythematosus (SLE), defined by the presence of ascites, pleural effusions and an …

Objectives Pulmonary involvement other than pulmonary artery involvement in Behcet’s
disease still remains an area of investigation. The aim of this study was to evaluate pulmonary …

In recent years, treat-to-target strategy and early intervention strategies with immunosuppressive
agents have attempted to improve the prognosis and outcome in patients with …

DEAR EDITOR, mRNA-based novel vaccines have been playing a critical role in controlling
the burden of the coronavirus disease 2019 pandemic on healthcare systems. Despite …

Immunoglobulin (Ig) G4-related disease (IgG4RD) is a chronic autoimmune disorder
characterized by dense lymphoplasmacytic infiltrations and fibrosis of storiform pattern. The most …

Long-term survival of patients with idiopathic inflammatory myopathies: anatomy of a single-centre
cohort Page 1 Clinical and Experimental Rheumatology 2022 Clinical and Experimental …

Discussion Behcet’s disease (BD) is primarily known by its mucocutaneous and ocular
manifestations [2]. However, vascular involvement in BD, which may be seen in about 40% of …

IgG4-related disease (IgG4-RD) is a fibroinflammatory condition that is characterized by
storiform fibrosis, infiltration of IgG4-positive lymphocytes, obliterative phlebitis, and high IgG4 …

DEAR EDITOR, In a retrospective analysis 7 years ago, it was estimated that 78% of patients
with inflammatory myositis were considered to have improved with rituximab (RTX)[1]. The …