Results 61 to 70 of about 12,403 (234)

Current approaches to diagnosing and treating eosinophilic granulomatosis with polyangiitis: The 2015 international guidelines [PDF]

Терапевтический архив, 2016
The 2015 international guidelines for the diagnosis and treatment of eosinophilic granulomatosis with polyangiitis, formerly known as the Churg-Strauss syndrome, are detailed and an attempt is made to expand an evidence base, by attracting more recent ...
T V Beketova, M Yu Volkov, E L Nasonov
doaj  

Diagnostic and therapeutic considerations in idiopathic hypereosinophilia with warm autoimmune hemolytic anemia. [PDF]

, 2015
Hypereosinophilic syndrome (HES) encompasses numerous diverse conditions resulting in peripheral hypereosinophilia that cannot be explained by hypersensitivity, infection, or atopy and that is not associated with known systemic diseases with specific ...
Brys, Adam K, Sheth, Milan R, Sohn, David D, Sweidan, Alexander J   +3 more
core   +1 more source

Rituximab for eosinophilic granulomatosis with polyangiitis: a systematic review of observational studies [PDF]

, 2021
Objective To analyse the available evidence about the use of rituximab (RTX) and other biologic agents in eosinophilic granulomatosis with polyangiitis (EGPA) patients and to provide useful findings to inform the design of future, reliable clinical ...
Angeletti A, Gabrielli A, Menditto VG, Olivari D, Pomponio G, Rocchi MBL, Rossetti G   +6 more
core   +1 more source

A case of hereditary alpha tryptasemia and presumptive eosinophilic granulomatosis with polyangiitis

Journal of Allergy and Clinical Immunology: Global
This case is notable for the potential overlap of hereditary alpha tryptasemia and eosinophilic granulomatosis with polyangiitis. The successful use of mepolizumab, initially for eosinophilic granulomatosis with polyangiitis but potentially benefiting ...
Sonia Iqbal, DO, Joseph A. Baxter, DO, Karla E. Adams, MD   +2 more
doaj   +1 more source

Real-world characteristics of “super-responders” to mepolizumab and benralizumab in severe eosinophilic asthma and eosinophilic granulomatosis with polyangiitis

ERJ Open Research, 2023
Background The current definition of severe eosinophilic asthma (SEA) super-responders to biologic treatment does not include patients with other eosinophil-based comorbidities.
Andrea Portacci, R. Campisi, E. Buonamico, S. Nolasco, C. Pelaia, N. Crimi, A. Benfante, Massimo Triggiani, G. Spadaro, M. Caiaffa, G. Scioscia, Aikaterini Detoraki, G. Valenti, F. Papia, Alessandra Tomasello, N. Scichilone, G. Pelaia, C. Crimi, G. E. Carpagnano   +18 more
semanticscholar   +1 more source

Types of Angiopathy in Experimental Autoimmune Disease in Rats [PDF]

, 2017
The purpose and objectives of this work were to study the nature of the heart, lungs and kidneys angiopathy in rats with a model of systemic autoimmune disease, carrying out comparisons of the results with extravasal morphological manifestations of the ...
Iegudina, Y. (Yelizaveta), Mikuksts, V. (Viktoriya), Syniachenko, O. (Oleg), Yakovlenko, P. (Pavel)   +3 more
core   +2 more sources

Ventricular Thrombus Formation Caused by Subendomyocardial Inflammation in Eosinophilic Granulomatosis With Polyangiitis

JACC: Case Reports
Cardiac involvement of eosinophilic granulomatosis with polyangiitis is a rare but life-threatening complication. We present a case of eosinophilic granulomatosis with polyangiitis with moderately impaired ventricular function forming a ventricular ...
Naoyuki Takahashi, MD, Takenori Ikoma, MD, PhD, Atsushi Sakamoto, MD, PhD, Kenichiro Suwa, MD, PhD, Mayu Fujihiro, MD, Kumiko Shimoyama, MD, PhD, Hayato Ohtani, MD, PhD, Satoshi Baba, MD, PhD, Noriyoshi Ogawa, MD, PhD, Yuichiro Maekawa, MD, PhD   +9 more
doaj   +1 more source

An immunogenetic perspective of ANCA-associated vasculitides

Egyptian Rheumatology and Rehabilitation, 2022
Background Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of small vessel vasculitides characterized by necrotizan vasculitis and inflammation.
A. Kocaaga, M. Kocaaga
doaj   +1 more source

New Insights into Pathogenesis and Treatment of ANCA-Associated Vasculitis: Autoantibodies and Beyond

Antibodies, 2023
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a group of rare systemic diseases affecting small-caliber vessels. The damage caused by AAV mainly involves the lung and kidneys. AAV includes three different types: granulomatosis with
Marino Paroli, Chiara Gioia, Daniele Accapezzato   +2 more
doaj   +1 more source

Eosinophilic Variant of Granulomatosis With Polyangiitis

Cureus, 2023
Granulomatosis with polyangiitis (GPA) is a multisystemic necrotizing vasculitis with a special tropism to the respiratory tract and the kidneys. Although uncommon, GPA may be associated with hypereosinophilia and limited organ involvement. In these cases, American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification ...
Fernandes, Rui L, Ornelas, Mariana F, Henriques, Ana C, Correia, Maria I, Faria, Teresa   +4 more
openaire   +2 more sources