Results 31 to 40 of about 331,732 (145)
Molecular targeted therapies for microscopic polyangiitis and granulomatosis with polyangiitis [PDF]
The Korean Journal of Internal Medicine, 2019 Clinical trials and observational studies have established cyclophosphamide (CY) or rituximab plus glucocorticoid (GC) as standard remission induction therapies in patients with microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA ...
Masayoshi Harigai +3 more
doaj +1 more source
ANCA Associated Mononeuritis Multiplex with Overlap in Vasculitic Syndromes [PDF]
Journal of Clinical and Diagnostic Research, 2017 Mononeuritis multiplex is a common manifestation of many illnesses which includes Hansen’s disease and certain types of systemic vasculitis. The Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis (AAV) is a group of rare diseases which ...
Ravi Anadure +3 more
doaj +1 more source
Microscopic polyangiitis: Modern concepts and treatment options [PDF]
, 2021 The article summarizes the modern concepts of microscopic polyangiitis (MPA), a primary ANCA-associated systemic necrotizing vasculitis without immune globulin deposition (pauci-immune) that affects mainly small vessels, while granulomatous inflammation ...
Zh. A. Murkamilova +6 more
core +1 more source
Microscopic polyangiitis with dermatomyositis
European Journal of Rheumatology, 2019 Abstract Dermatomyositis is a rare autoimmune disease with a heterogeneous presentation that often has multiple extramuscular manifestations, although it does not typically involve the renal function. A 62-year-old female presented with proximal muscle weakness and rashes, which are classic symptoms of dermatomyositis without creatine kinase (CK ...
Erin M, Bauer, Ernest, Brahn
openaire +2 more sources
Научно-практическая ревматология, 2021 The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of severe life-threatening autoimmune diseases, and one of the most important problems in practical rheumatology.
T. V. Beketova +2 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2016 Background The data from cohorts of childhood-onset granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) remain scarce and heterogeneous. We aimed to analyse the features at presentation, therapeutic approaches and the disease course
Michele Iudici +5 more
doaj +1 more source
Hearing Loss and Kidney Dysfunction: Finding a Unifying Diagnosis
Case Reports in Medicine, 2013 Microscopic polyangiitis (MPA) is a systemic vasculitis that affects small caliber vessels, with renal and lung compromise. Diagnosis can be challenging; timely diagnosis and treatment are important to prevent devastating complication, particularly renal
Praveena Iruku +4 more
doaj +1 more source
Microscopic polyangiitis [PDF]
, 2021 La poliangeítis microscópica es una enfermedad idiopática autoinmunitaria caracterizada por una vasculitis sistémica necrosante, no granulomatosa, de pequeños o medianos vasos, asociada a la presencia de anticuerpos citoplasmáticos antineutrófilos (Anti ...
Argote, Arturo César, Merlano, Itala
core
Clinical Case Reports, 2021 Unexplained deep vein thrombosis may justify screening for antineutrophil cytoplasmic antibody‐associated vasculitis as it can be an unusual presentation of this disease.
Mouna Jerbi +6 more
doaj +1 more source
Occupational Silica Exposure as a Potential Risk for Microscopic Polyangiitis
, 2023 Microscopic polyangiitis is an important and common component of cytoplasmic antibody–associated vasculitides that can lead to serious morbidity and even death. A clear causative etiology has not been identified.
Hakan Akdam +11 more
core +1 more source