Results 101 to 110 of about 14,549 (184)

Quantitative computed tomography in interstitial lung disease related to ANCA‐associated vasculitis: First insights from a mono‐centric retrospective cohort

Rheumatology &Autoimmunity, EarlyView.
Alarico Ariani, Mario Silva, Giovanni M. Rossi, Marco Delsante, Andrea Becciolini, Enrico Fiaccadori, Augusto Vaglio, Nicola Sverzellati   +7 more
wiley   +1 more source

Intracerebral Hemorrhage During the Chronic Phase of Eosinophilic Granulomatosis With Polyangiitis: A Case Report Emphasizing Cerebrovascular Vulnerability

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of small‐vessel vasculitis typically associated with eosinophilia, asthma, and systemic inflammation. Although peripheral neuropathies are relatively common, central nervous system involvement, especially intracerebral hemorrhage during the remission phase of EGPA, is uncommon,
Shinya Watanabe, Masatoshi Kasuya, Yasushi Shibata   +2 more
wiley   +1 more source

Wegener-granulomatosis [PDF]

, 2015
A Wegener-granulomatosis a kis és közepes átmérőjű erek granulomaképződéssel járó nekrotizáló gyulladása. Súlyosság és klinikai megjelenés szempontjából a betegség igen széles skálát mutat.
Csákó László,, Domján, Gyula, Gadó, Klára, Z Szabó László,   +3 more
core   +1 more source

An Atypical Presentation of Tubulointerstitial Nephritis With Uveitis (TINU) in an Older Patient Requiring Emergency Dialysis: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Tubulointerstitial nephritis with uveitis (TINU) is an immune‐mediated systemic disorder most commonly described in adolescents and young adults, and its recognition in older patients remains challenging. We report the case of a 58‐year‐old woman who presented with systemic symptoms and rapidly progressive acute kidney injury.
Yuli Yang, Yangna Shi, Jian Li, Jing Meng, Wenyu Gong   +4 more
wiley   +1 more source

Anticuerpos anticitoplasma del neutrófilo en la clasificación de las vasculitis sistémicas

Revista Cubana de Medicina, 2003
La detección de los anticuerpos anticitoplasma del neutrófilo (ANCA) constituye el diagnóstico inmunológico de las vasculitis sistémicas. Este trabajo estuvo dirigido a probar la utilidad clínica del método de inmunofluorescencia indirecta (IFI) sobre ...
Elena Kokuina, Milton Sánchez Basulto, Ana María Arias Prieto, Ana María Guerreiro Hernández   +3 more
doaj  

Similarities and Differences Between Patients Diagnosed with ANCA-Associated Vasculitis Who Are Positive and Negative for ANCA: University Clinic Practice and Expertise

Medicina
Background and objective. Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) affects small- to medium-sized vessels and is characterized by the production of ANCAs. The ANCA-negative term is used if the patient otherwise fulfills the
Giedre Dereseviciene, Jolanta Dadoniene, Dalia Miltiniene   +2 more
doaj   +1 more source

CpG oligodeoxynucleotide stimulates production of anti-neutrophil cytoplasmic antibodies in ANCA associated vasculitis

BMC Immunology, 2008
Background Wegener's Granulomatosis and Microscopic Polyangiitis are life-threatening systemic necrotizing vasculitides of unknown aetiology. The appearance of circulating antibodies to neutrophil cytoplasmic antigens (ANCA) is strongly associated with ...
Sarvestani Ghafar, Patel Mittal, Nitschke Jodie, Jeffs Lisa, Hurtado Plinio R, Cassidy John, Hissaria Pravin, Gillis David, Au Peh Chen   +8 more
doaj   +1 more source

Neutrophil extracellular traps mediate transfer of cytoplasmic neutrophil antigens to myeloid dendritic cells toward ANCA induction and associated autoimmunity. [PDF]

, 2012
Antineutrophil cytoplasmic antibodies (ANCAs) target proteins normally retained within neutrophils, indicating that cell death is involved in the autoimmunity process. Still, ANCA pathogenesis remains obscure.
Abdgawad, Alcorta, Barbara Cappetti, Bennett, Bianchi, Brinkmann, Carla Guarnotta, Cassatella, Caterina Vitali, Chin, Claudia Chiodoni, Claudio Tripodo, Clayton, Colombo, Cristiana Guiducci, Di Carlo, Dittmar, Donnelly, Drenkard, Falk, Fuchs, Gaipl, Galeazzi, Garcia-Romo, Gilligan, Griffith, Guiducci, Jarius, Kantari, Kessenbrock, Lande, Manolova, Mariella Parenza, Mario P. Colombo, Martinelli, Metzler, Munafo, Nagata, Nathan, Patrizia Casalini, Patry, Potter, Pradhan, Remijsen, Sabina Sangaletti, Sangaletti, Santiago-Raber, Silvia Piconese, Specks, Spronk, Steinman, Tripodo, van der Geld, van Timmeren, Villanueva, Wernick, Witko-Sarsat, Ziegler-Heitbrock   +57 more
core   +1 more source

Expanded Phenotype of PAX2‐Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Nadira Sultana, Abdullah Al Mamun, Afroza Begum   +2 more
wiley   +1 more source

Antineutrophilic Cytoplasmic Antibody–Positive Vasculitis Associated With Thromboangiitis Obliterans in a Middle-Aged Man

Annals of Internal Medicine: Clinical Cases
Antineutrophilic cytoplasmic antibody (ANCA)-associated vasculitides are autoimmune diseases with multisystem manifestations. We report the case of a 55-year-old Asian man with a history of cigarette smoking who presented with ischemic lesions of the ...
Naushad Abid, Hamzah Naushad Siddiqui
doaj   +1 more source