Results 101 to 110 of about 21,257 (220)

Fulminant Wegener's granulomatosis: A case report [PDF]

, 2013
Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž., Kandolf-Sekulović Lidija, Zečević Radoš D., Zolotarevski Lidija   +3 more
core   +1 more source

Tracheobronchial Stenosis in Granulomatosis With Polyangiitis: Immunosuppressant Use and Airway Dilation Frequency

ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Objective Tracheobronchial stenosis (TBS) occurs in 13% to 27% of patients with granulomatosis with polyangiitis (GPA) and may cause life‐threatening airway compromise. Despite advances in treatment, TBS remains difficult to manage, with frequent relapses and high procedural burden.
Brendan Denvir, Ami A. Shah, Alexander T. Hillel, Philip Seo, Ji Soo Kim, Brendan Antiochos   +5 more
wiley   +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

The Role of Extracorporeal Membrane Oxygenation in Cardiopulmonary Dysfunction Due to Rheumatologic Diseases: A Systematic Review

ACR Open Rheumatology, Volume 8, Issue 4, April 2026.
Objective This systematic review documents the current status of extracorporeal membrane oxygenation (ECMO) use in patients with complications of rheumatologic diseases. Methods Following Preferred Reporting Items for Systematic Reviews and Meta Analyses 2020 guidelines, we conducted a systematic review of studies published from January 2019 to ...
Kari L. Falaas, Lyubov Y. Tiegs, Nicole Theis‐Mahon, Elie Gertner   +3 more
wiley   +1 more source

Granulomatosis with Polyangiitis

Journal of Japan Society of Immunology & Allergology in Otolaryngology, 2019
Granulomatosis with polyangiitis (GPA) is a small-vessel necrotizing vasculitis that most characteristically affects the ear, nose, and throat (ENT), lungs, and/or kidneys. The median age at diagnosis is in the fifth decade, but children and older people can be affected.
openaire   +3 more sources

Aortic Valve Perforation in Pediatric Granulomatosis With Polyangiitis: A Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Granulomatosis with polyangiitis, formerly Wegener's granulomatosis, is a rare antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis primarily affecting the respiratory tract and kidneys. Cardiovascular involvement, particularly valvular disease, is rare, especially in pediatric patients.
Libor Svoboda, Martin Scholten, Corinna Jugel, Johanna Buschner, Christian Schürer, Alexandra Kiess   +5 more
wiley   +1 more source

Dysphagia as the Sole Presentation of Lateral Medullary Syndrome in an Octagerian: A Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Lateral medullary syndrome (LMS) or Wallenberg's syndrome is usually caused by a cerebrovascular accident of the vertebral artery or the posterior inferior cerebellar artery (PICA), leading to damage to the dorsolateral aspects of the medulla oblongata.
Abera Kuma, Bereket A. Tegene, Sosena Sheleme, Shamil Nuri, Abdulkerim Girma, Sinetibeb Tadesse Amsalu   +5 more
wiley   +1 more source

T Cells in Vascular Inflammatory Diseases [PDF]

, 2014
Inflammation of the human vasculature is a manifestation of many different diseases ranging from systemic autoimmune diseases to chronic inflammatory diseases, in which multiple types of immune cells are involved. For both autoimmune diseases and chronic
Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Abdulahad, Ait-Oufella, Ait-Oufella, Allez, Almanzar, Ammirati, Appay, Bauer, Beeton, Beeton, Beeton, Bettelli, Brouwer, Brouwer, Brown, Cahalan, Capraru, Caruso, Chandy, Chavele, Cohen Tervaert, Davenport, de Boer, de Boer, de Leeuw, de Menthon, Deng, Ebert, Elhage, Erbel, Erbel, Ettinger, Fazilleau, Fontenot, Free, Frostegard, Gan, Gao, Gao, Gephardt, Geri, Gocke, Gotsman, Groh, Gupta, Hauer, Hoshino, Hoshino, Hu, Huber, Imura, Ivanov, Jennette, Jennette, Jonasson, Jonasson, Jovanovic, Kallenberg, Karnell, Kellner, King, King, Kjellev, Klapa, Koch Hansen, Koenen, Komocsi, Laan, Lamprecht, Lamprecht, Langford, Lee, Liston, Lockwood, Mallat, Mallat, Mangan, Matheu, Mestas, Moosig, Morgan, Muller, Niebuhr, Nogueira, Odobasic, Ogasawara, Ooi, Ordonez, Panettieri, Popa, Roselaar, Ruth, Saadoun, Saito, Saito, Samson, Samson, Sanders, Schmitt, Schmitt, Schonermarck, Seta, Smith, Stegeman, Stegeman, Taleb, Terrier, Tse, Valencia, van Es, van Loosdregt, Vincenti, Wang, Weidner, Whitman, Whitman, Whitman, Wilde, Wulff, Xia, Zhou, Zhou, Zhou, Zielinski   +128 more
core   +2 more sources

Straight to Phase III: Model‐Informed Approach Speeds Depemokimab Clinical Development in Interleukin‐5‐Driven Diseases

Clinical Pharmacology &Therapeutics, Volume 119, Issue 4, Page 1005-1015, April 2026.
Straight to Phase III: Model‐informed approach speeds depemokimab clinical development in interleukin‐5‐driven diseases. IL‐5, a key mediator of type 2 inflammation, underlies various diseases, including severe asthma, CRSwNP, EGPA, and HES. Reduction in blood eosinophil count (BEC), a biomarker of IL‐5 activity, is commonly used to evaluate the ...
Chiara Zecchin, Stein Schalkwijk, Isabelle J. Pouliquen, Alienor Berges, Nicholas Bird, Richard Follows, Daren Austin   +6 more
wiley   +1 more source

Granulomatosis with Polyangiitis Presenting with Coronary Artery and Pericardial Involvement

Case Reports in Radiology, 2015
Granulomatosis with polyangiitis is a systemic disease resulting in necrotizing vasculitis of small- and medium-sized vessels. Cardiac involvement is rare and when present usually manifests with pericarditis and coronary artery vasculitis. We report here
Rohit Dewan, Humberto E. Trejo Bittar, Joan Lacomis, Iclal Ocak   +3 more
doaj   +1 more source