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Article
Relapsing polychondritis: clinical updates and new differential diagnoses
Relapsing polychondritis is a rare inflammatory disease characterized by recurrent inflammation of cartilaginous structures, mainly of the ears, nose and respiratory tract, with a broad spectrum of accompanyin...
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Article
Reduced peripheral blood dendritic cell and monocyte subsets in MDS patients with systemic inflammatory or dysimmune diseases
Systemic inflammatory and autoimmune diseases (SIADs) occur in 10–20% of patients with myelodysplastic syndrome (MDS). Recently identified VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndr...
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Article
Open AccessMyelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylation
Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders, representing high risk of progression to acute myeloid leukaemia, and frequently associated to somatic mutations, notably in the epigenetic r...
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Article
Open AccessResponse letter to “Latent class analysis of 216 patients with adult-onset Still’s disease” by Sugiyama et al.
Sugiyama et al. recently described in “Latent class analysis of 216 patients with adult-onset Still’s disease,” baseline characteristics, laboratory tests, treatment, relapse, and death of adult-onset Still’s ...
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Article
Massive vulvar edema revealing idiopathic systemic capillary leak syndrome
Idiopathic systemic capillary leak syndrome is a rare disease characterized by recurrent episodes of hypotension, hypoalbuminemia and peripheral edema caused by capillary hyperpermeability with approximately 3...
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Article
Incidence of giant cell arteritis in six districts of Paris, France (2015–2017)
This prospective population-based study estimated the incidence of giant cell arteritis (GCA) in northeastern Paris. GCA cases diagnosed between 2015 and 2017 were obtained from local hospital and community-ba...
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Article
Clinical phenotype and cytokine profile of adult IgA vasculitis with joint involvement
Joint involvement can be observed during the course of adult IgA vasculitis (IgAV). However, clinical picture, prognosis, or pathophysiological data associated with this condition have been overlooked. We aime...
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Article
UBA1 gene mutation in giant cell arteritis
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Article
Open AccessNon-criteria manifestations in primary antiphospholipid syndrome: a French multicenter retrospective cohort study
From this retrospective study, we aimed to (1) describe the prevalence and characteristics of non-criteria features in primary antiphospholipid syndrome (p-APS) and (2) determine their prognostic value.
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Article
Genomic landscape of MDS/CMML associated with systemic inflammatory and autoimmune disease
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Article
Prevalence of UBA1 mutations in MDS/CMML patients with systemic inflammatory and auto-immune disease
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Article
Systemic sclerosis is associated with lower limb vascular stiffness and microvascular impairment: results from a prospective study
Systemic sclerosis (SSc) is a connective tissue disease characterized by microangiopathy. Peripheral arterial disease, increasingly studied during SSc, is responsible for digital ulcers, associated with a high...
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Article
Open AccessTFH cells in systemic sclerosis
Systemic sclerosis is an autoimmune disease characterized by excessive dermal fibrosis with progression to internal organs, vascular impairment and immune dysregulation evidenced by the infiltration of inflamm...
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Article
Open AccessPrevalence of cardiovascular risk factors, the use of statins and of aspirin in Takayasu Arteritis
The aim of this study was to assess the prevalence of cardiovascular risk factors in TAK, to describe the use of aspirin and statins and the risk factors associated with vascular ischemic complications and rel...
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Article
New insights on IgA vasculitis with underlying solid tumor: a nationwide French study of 30 patients
IgA vasculitis (IgAV) frequently occurs during or after a mucosal infection; it also rarely occurs in patients with cancer. We hypothesized that cancer could impact the baseline characteristics and/or outcome ...
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Article
Autologous hematopoietic stem cell transplantation with reduced-intensity conditioning regimens in refractory Takayasu arteritis: a retrospective multicenter case-series from the Autoimmune Diseases Working Party (ADWP) of the European Society for Blood and Marrow Transplantation (EBMT)
Autologous hematopoietic stem cell transplantation (AHSCT) has emerged as a promising treatment option in severely affected and refractory patients with autoimmune diseases. This is a retrospective survey of p...
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Article
Open AccessEarly trajectories of skin thickening are associated with severity and mortality in systemic sclerosis
Systemic sclerosis (SSc) is a severe and highly heterogeneous disease. The modified Rodnan skin score (mRSS) is a widely used tool for the assessment of the extent and degree of skin thickness. This study aime...
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Article
Transfusion-related acute lung injury (TRALI) after intravenous immunoglobulins: French multicentre study and literature review
Transfusion-related acute lung injury (TRALI), defined as the onset of acute respiratory distress after blood transfusion, is a rare complication which is a leading cause of transfusion related-mortality. In t...
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Article
Open AccessPET/MRI in large-vessel vasculitis: clinical value for diagnosis and assessment of disease activity
Diagnosis of large vessel vasculitis (LVV) and evaluation of its inflammatory activity can be challenging. Our aim was to investigate the value of hybrid positron-emission tomography/magnetic resonance imaging...
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Article
Proportion of Cytotoxic Peripheral Blood Natural Killer Cells and T-Cell Large Granular Lymphocytes in Recurrent Miscarriage and Repeated Implantation Failure: Case–Control Study and Meta-analysis
We aimed to compare the proportion of peripheral blood natural killer (NK) cells (CD3–CD56+) and T-cell large granular lymphocytes (CD8+CD57+) during preconception in a homogenous group of women with unexplained ...
