Results 61 to 70 of about 951,952 (191)

What is new in the management of rapidly progressive glomerulonephritis? [PDF]

, 2015
Rapidly progressive glomerulonephritis (RPGN) results from severe crescentic damage to glomeruli and leads to irreversible kidney failure if not diagnosed and managed in a timely fashion.
Greenhall, GHB, G. H. B. Greenhall, Salama, AD, A. D. Salama   +3 more
core   +1 more source

Red blood cell distribution width as a useful indicator to predict systemic vasculitis in patients with cutaneous vasculitis

, 2015
Cutaneous vasculitis can be limited to skin or a manifestation of primary systemic vasculitis. However, there are no definite markers to predict systemic involvements.
이민걸, 김대석, 김도영, 김태균, 김성희   +4 more
core   +1 more source

The current classification of systemic vasculitides

Терапевтический архив, 2014
Systemic vasculitides (SV) are severe multiorgan diseases whose early diagnosis and treatment can significantly improve prognosis. Improving the classification of SV may lead to a significant reduction in the likelihood of diagnostic errors.
T V Beketova
doaj  

Central Nervous System Vasculitis

, 2023
Central nervous system vasculitis (CNSV) is a group of disorders leading to inflammatory vasculopathy within the brain, spinal cord, and leptomeninges. CNSV is divided into primary angiitis of the central nervous system (PACNS) and secondary CNSV based ...
Ken Uchino, Hajj-Ali, RA, Uchino, K, Moein Amin, Amin, M, Rula A. Hajj-Ali   +5 more
core   +1 more source

An Atypical Case of Vasculitis: When ‘Occult’ 18FDG-PET Scan Findings Create a Classification Dilemma

European Journal of Case Reports in Internal Medicine, 2019
We describe a 66-year old patient with a recurrent ulcer on her right ankle. Biopsy revealed medium-vessel vasculitis consistent with cutaneous polyarteritis nodosa.
Elena Lopez-Francos, Sammy Place, Daphnee Delplace, Frédéric Vandergheynst   +3 more
doaj   +1 more source

[Systemic ANCA-associated vasculitis--diagnosis and therapy]

, 2008
ANCA-associated vasculitis represents a group of small-vessel vasculitides, including Wegener's granulomatosis, microscopic polyangiitis and the Churg-Strauss-syndrome.
Hess, Christof, Eisenberger, Ute
core  

Increased serum levels of macrophage migration inhibitory factor (MIF) in patients with microscopic polyangiitis

Open Access Rheumatology: Research and Reviews, 2009
Hirohito Kanemitsu, Mizuho Matsunawa, Kuninobu Wakabayashi, Michihito Sato, Ryo Takahashi, Tsuyoshi Odai, Takeo Isozaki, Nobuyuki Yajima, Yusuke Miwa, Tsuyoshi KasamaDivision of Rheumatology, Department of Medicine, Showa University School of Medicine ...
Hirohito Kanemitsu, Mizuho Matsunawa, Kuninobu Wakabayashi, Michihito Sato, et al.   +4 more
doaj  

Multi-Modality Imaging in Vasculitis

Diagnostics
Systemic vasculitides are a rare and complex group of diseases that can affect multiple organ systems. Clinically, presentation may be vague and non-specific and as such, diagnosis and subsequent management are challenging.
Mohamed N. Allam, Nima Baba Ali, Ahmed K. Mahmoud, Isabel G. Scalia, Juan M. Farina, Mohammed Tiseer Abbas, Milagros Pereyra, Moaz A. Kamel, Kamal A. Awad, Yuxiang Wang, Timothy Barry, Steve S. Huang, Ba D. Nguyen, Ming Yang, Clinton E. Jokerst, Felipe Martinez, Chadi Ayoub, Reza Arsanjani   +17 more
doaj   +1 more source

Urticarial vasculitis coexisting with primary myelofibrosis – a case report

Przegląd Dermatologiczny, 2017
Introduction . Urticarial vasculitis is a subtype of cutaneous leukocytoclastic vasculitis. The disease often accompanies systemic disorders, including hematologic malignancies, connective tissue diseases, and infectious diseases, or may be drug-induced.
Radomir Reszke, Adam Reich
doaj   +1 more source

Inflammatory muscle involvement in systemic vasculitis: A systematic review

, 2022
Vasculitis are severe systemic autoimmune diseases which may involve different organs and systems. Conversely, muscles do not represent an organ commonly involved by systemic vasculitis and myositis is not include among any classification or diagnostic ...
Mazzei M. A., D'Alessandro R., Vallifuoco G., Pata A. P., Falsetti P., Gentileschi S., Cantarini L., Frediani B., Bargagli E., d'Alessandro M., Al Khayyat S. G., D'Ignazio E., Bardelli M., Conticini E., Fabiani C., Guarnieri A., Baldi C.   +16 more
core   +1 more source