Results 21 to 30 of about 355,295 (195)

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, Coimbatore Narayanan, Govindraj Varadraj, Bevinahalli Nandeesh   +3 more
doaj   +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

Review of guideline for the management of ANCA-associated vasculitis, presented in 2021 by the American College of Rheumatology/Vasculitis Foundation

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, I. Yu. Popov, V. V. Babak   +2 more
doaj   +1 more source

Childhood-onset granulomatosis with polyangiitis and microscopic polyangiitis: systematic review and meta-analysis

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, Pierre Quartier, Benjamin Terrier, Luc Mouthon, Loïc Guillevin, Xavier Puéchal   +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, Puja Karanth, Hannah Tiu, Charity Kankam, Khaldoon Shaheen   +4 more
doaj   +1 more source

Deep vein thrombosis: An unusual way of revealing microscopic polyangiitis. Deep vein thrombosis in microscopic polyangiitis

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, Hiba Ghabi, Hanene Gaied, Mariem Khadhar, Raja Aoudia, Rim Goucha, Taieb Ben Abdallah   +6 more
doaj   +1 more source

Update of Management of ANCA-Associated Vasculitis

Journal of Clinical Rheumatology and Immunology, 2021
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is associated with significant morbidity and mortality. Management of AAV is divided into induction of remission and maintenance of remission.
Hoi San Tang, Shirley King Yee
doaj   +1 more source

International guidelines for the management ofANCA-associated systemic vasculitides

Современная ревматология, 2019
The paper deals with international guidelines for the management of antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (SVs) that are a group of severe life-threatening immune-mediated diseases. This group includes granulomatosis
T. V. Beketova
doaj   +1 more source

Interstitial lung disease in microscopic polyangiitis and granulomatosis with polyangiitis: demographic, clinical, serological and radiological features of an Italian cohort from the Italian Society for Rheumatology

, 2022
Interstitial lung disease (ILD) has been described as a possible pulmonary involvement in antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitides (AAV), mainly granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). Aim of
Felicetti, Mara, De Vita, Salvatore, Cantini, Fabrizio, Dallagiacoma, Gloria, Monti, Sara, Kaleci, Shaniko, Sebastiani, Marco, Study Group of the Italian Society for Rheumatology (SIR), Izzo, Raffaella, Giollo, Alessandro, Cassone, Giulia, Conticini, Edoardo, Padoan, Roberto, Caporali, Roberto, Rossini, Maurizio, Dagna, Lorenzo, Montecucco, Carlomaurizio, Muratore, Francesco, Quartuccio, Luca, Manfredi, Andreina, Govoni, Marcello, Nannini, Carlotta, Berti, Alvise, Frediani, Bruno, Cariddi, Adriana, Argolini, Lorenza Maria, Emmi, Giacomo, Bettio, Silvano, Salvarani, Carlo, Dejaco, Christian, Govoni M., Padoan R., Manfredi A., Bettio S., Monti S., Cantini F., Muratore F., Montecucco C., Salvarani C., Quartuccio L., Cariddi A., Quartuccio, L., Dallagiacoma G., Sebastiani M., Conticini E., Emmi G., Caporali R., Rossini M., Frediani B., Dagna L., Giollo A., Kaleci S., Felicetti M., Dejaco C., De Vita S., Nannini C., Izzo R., Berti A., Argolini L. M., De Vita, S., Cassone G.   +60 more
core   +1 more source

A case report of microscopic polyangiitis presenting as diffuse pulmonary symptoms with no renal involvement [PDF]

, 2020
Microscopic polyangiitis (MPA) is a small blood vascular disorder, but with presence of no granulomas. This is a pauci- immune disorder vessels which lead to vascular inflammation and then later, it can lead to organ microscopic polyangiitis.
Acharya, Pavan, Khan, Rafe, Singhvi, Shreyans D., Patel, Monila, Singh, Preksha   +4 more
core   +1 more source