Results 101 to 110 of about 355,295 (195)

Schematic diagram showing the number of study participants in each group.

, 2015
AAV = ANCA associated vasculitis; GPA = granulomatosis with polyangiitis (Wegener’s); MPA = microscopic polyangiitis; EGPA = eosinophilic granulomatosis with polyangiitis.
H. Becker (792081), C. Sauerland (792080), H. Schotte (792084), S. Reuter (792082), A. Jacobi (792083), B. Schlüter (792079), P. Willeke (792078)   +6 more
core   +1 more source

Rituximab for the treatment of eosinophilic granulomatosis with polyangiitis (Churg-Strauss).

, 2016
Conventional treatment of eosinophilic granulomatosis with polyangiitis (EGPA) (Churg-Strauss) with glucocorticoids, with or without additional immunosuppressive drugs, is limited by partial efficacy, frequent toxicity and a high relapse rate.
Hot, A, Moosig, F, Jayne, D R W, Merkel, P A, Smith, R, Guerry, M-J, Guillevin, L, Sivasothy, P, Amudala, N, Arndt, F, Lund University., Mohammad, Aladdin, Mohammad, Aladdin,   +12 more
core   +1 more source

A case of simultaneously diagnosed microscopic polyangiitis and lung adenocarcinoma

An octogenarian female who developed edema in the lower extremities and exertional dyspnea was admitted to our hospital. A diagnosis of lung carcinoma was made from radiographic images and lung biopsy findings.
Nagayoshi, Yohsuke, Horai, Yoshiro, Mori, Hideki, Michitsuji, Tohru, Ito, Masahiro, Kawakami, Atsushi, Iwanaga, Nozomi, Kawaguchi, Yushi, Kawahara, Chieko, Izumi, Yasumori   +9 more
core  

Granulomatosis with polyangiitis – diagnostic difficulties?

, 2014
Granulomatosis with polyangiitis (GPA) is characterized by necrotic vasculitis of the medium and small vessels, granuloma formation and presence of antineutrophil cytoplasmic antibodies against proteinase-3 in serum.
Marta Madej, Piotr Wiland, Katarzyna Białowąs, Agnieszka Matuszewska   +3 more
core   +1 more source

Microscopic polyangiitis presenting as idiopathic pulmonary fibrosis

The most detectable form of pulmonary fibrosis in MPA (microscopic polyangiitis) is UIP (usual interstitial pneumonia), occurring in 48 % of MPA patients with pulmonary fibrosis.
Brittany Duchene
core   +1 more source

Microscopic Polyangiitis with an Atypical Presentation

Indian Journal of Rheumatology, 2023
Preetam Rajgopal Acharya, Deepthi Sharma, Sindhu Kamath, Sajjan Shenoy, Rahul Magazine   +4 more
doaj   +1 more source

Place in therapy of rituximab in the treatment of granulomatosis with polyangiitis and microscopic polyangiitis

ImmunoTargets and Therapy, 2015
Shivani Shah, Duvuru Geetha Department of Medicine, Division of Nephrology, Johns Hopkins University School of Medicine, Baltimore, MD, USA Abstract: Granulomatosis with polyangiitis and microscopic polyangiitis are small vessel vasculitides ...
Shah S, Geetha D
doaj  

Skin Ulcers In a Patient Afflicted With Microscopic Polyangiitis

, 2009
Systemic vasculitis is a group of heterogeneous diseases characterized by inflammation and blood vessel walls necrosis. Usually the skin is one of the first organs involved, especially with damage of small to medium size vessels.
Cimillo Manuela, CALVIERI, Stefano, Mattozzi Carlo, Richetta Antonio G., Maiani Elisa, Carboni Valentina, Giancristoforo Simona, D'Epiro Sara, Carlomagno Valentina   +8 more
core  

Microscopic polyangiitis with pulmonary involvement: Case Report. [PDF]

Front Med (Lausanne)
Ochoa-Andrade M, Muñoz S, González B, Rojas M, Mideros T, Santana J, Quishpe A, Velasteguí J, Uguña F.   +8 more
europepmc   +1 more source

Microscopic Polyangiitis With Pituitary Dysfunction and Spontaneous Renal Aneurysm Rupture. [PDF]

J Med Cases
Liang SJ, Zheng QY, Dai HZ.
europepmc   +1 more source