Results 41 to 50 of about 9,401 (207)

Clinical presentation and outcome of pediatric ANCA-associated glomerulonephritis [PDF]

, 2016
Background Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a small- and medium-sized vasculitis classically seen in adult patients, with peak onset near the fifth to seventh decade of life.
Andreoli, Sharon P., Kouri, Anne M.
core   +1 more source

Cutaneous Vasculitis as Early Presentation of Eosinophilic Granulomatosis with Polyangiitis without Systemic Symptoms

Oman Medical Journal, 2019
Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) is a rare vasculitis in children. It commonly presents with respiratory symptoms, especially asthma, allergic rhinitis, and peripheral eosinophilia.
Wahinuddin Sulaiman, Aris Chandran Abdullah, Sin Fah Chung, Norain Karim, Jyi Jong Tang   +4 more
doaj   +1 more source

ANCA-associated vasculitis – Should we change the standard of care? [PDF]

, 2015
Collaborative clinical trials over the last 25 years have revolutionised the care of patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. This has led to production of management recommendations and standards of care.
Bligny, Bourgarit, Choi, de Groot, De Groot, Fauci, Faurschou, Finkielman, Flossmann, Ghosh, Guillevin, Han, Harper, Hauer, Hoffman, Jayne, Jennette, Jennette, Koldingsnes, Leavitt, Luqmani, Mahr, Masi, Mooney, Mooney, Mukhtyar, Mukhtyar, Mukhtyar, Mukhtyar, Nataraja, Ntatsaki, Pagnoux, Pradhan, Rahmattulla, Rao, Reinhold-Keller, Sharma, Sorensen, Stone, Stone, Suppiah, Talar-Williams, Walsh, Watts, Watts, Watts   +45 more
core   +1 more source

A rare case report of polyangiitis overlap syndrome: granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis

BMC Pulmonary Medicine, 2018
Background Granulomatosis with polyangiitis (GPA) is a systemic ANCA-associated vasculitis characterized by necrotizing granulomatous inflammation and a predilection for the upper and lower respiratory tract. Eosinophilic granulomatosis with polyangiitis
Michele V. Quan, Stephen K. Frankel, Mehrnaz Maleki-Fischbach, Laren D. Tan   +3 more
doaj   +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

THE 2015 INTERNATIONAL GUIDELINES FOR THE DIAGNOSIS AND TREATMENT OF EOSINOPHILIC GRANULOMATOSIS WITH POLYANGIITIS

Научно-практическая ревматология, 2016
In 2015, guidelines for the diagnosis and treatment of eosinophilic granulomatosis with polyangiitis, formerly known as Churg-Strauss syndrome, were prepared with the participation of experts from 5 countries of Europe, the USA, and Canada, who ...
T. V. Beketova, M. Yu. Volkov
doaj   +1 more source

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

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

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