Results 21 to 30 of about 6,124 (160)

Deep vein thrombosis: An unusual way of revealing microscopic polyangiitis. Deep vein thrombosis in microscopic polyangiitis

Clinical Case Reports, 2021
Unexplained deep vein thrombosis may justify screening for antineutrophil cytoplasmic antibody‐associated vasculitis as it can be an unusual presentation of this disease.
Mouna Jerbi, Hiba Ghabi, Hanene Gaied, Mariem Khadhar, Raja Aoudia, Rim Goucha, Taieb Ben Abdallah   +6 more
doaj   +1 more source

Update of Management of ANCA-Associated Vasculitis

Journal of Clinical Rheumatology and Immunology, 2021
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is associated with significant morbidity and mortality. Management of AAV is divided into induction of remission and maintenance of remission.
Hoi San Tang, Shirley King Yee
doaj   +1 more source

International guidelines for the management ofANCA-associated systemic vasculitides

Современная ревматология, 2019
The paper deals with international guidelines for the management of antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (SVs) that are a group of severe life-threatening immune-mediated diseases. This group includes granulomatosis
T. V. Beketova
doaj   +1 more source

Asbestos and Probable Microscopic Polyangiitis

Canadian Respiratory Journal, 2004
Several inorganic dust lung diseases (pneumoconioses) are associated with autoimmune diseases. Although autoimmune serological abnormalities are common in asbestosis, clinical autoimmune/collagen vascular diseases are not commonly reported.
George S Rashed Philteos, Kelly Coverett, Rajni Chibbar, Heather A Ward, Donald W Cockcroft   +4 more
doaj   +1 more source

Various patterns of acute alveolar haemorrhage in patients with microscopic polyangiitis: a clinicopathological study of four cases

Polish Journal of Pathology, 2019
It is well known that acute alveolar haemorrhage (AAH) is attributed to capillaritis in most cases with microscopic polyangiitis (MPA). In this article, we explore the cause of alveolar haemorrhage in MPA patients. In the present study, we extracted four
Naoto Kuroda, Kenji Yorita, Kei Sakamoto, Kazuya Tsuji   +3 more
doaj   +1 more source

Microscopic polyangiitis: an incidental finding in a patient with stroke

Journal of Community Hospital Internal Medicine Perspectives, 2020
Microscopic polyangiitis (MPA) is a primary systemic vasculitis characterized by inflammation of small-sized vessels associated with the presence of anti-neutrophilic cytoplasmic antibodies.
Abubakar Tauseef, Muhammad Sohaib Asghar, Mariam Amir, Maryam Zafar, Ayesha Anum, Haris Alvi, Mustafa Dawood, Uzma Rasheed, Mohammed Akram, Nisar Ahmed   +9 more
doaj   +1 more source

Microscopic polyangiitis presented with biopsy-confirmed pleuritis

Monaldi Archives for Chest Disease, 2018
We describe a case of microscopic polyangiitis manifested as pleuritis confirmed by thoracoscopic biopsy. An 80-year-old man presented with a three-day history of shortness of breath and cough.
Naoto Ishimaru, Hisashi Ohnishi, Mao Fujii, Masako Yumura, Sho Yoshimura, Saori Kinami   +5 more
doaj   +1 more source

An immunogenetic perspective of ANCA-associated vasculitides

Egyptian Rheumatology and Rehabilitation, 2022
Background Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are a group of small vessel vasculitides characterized by necrotizan vasculitis and inflammation.
A. Kocaaga, M. Kocaaga
doaj   +1 more source

New Insights into Pathogenesis and Treatment of ANCA-Associated Vasculitis: Autoantibodies and Beyond

Antibodies, 2023
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a group of rare systemic diseases affecting small-caliber vessels. The damage caused by AAV mainly involves the lung and kidneys. AAV includes three different types: granulomatosis with
Marino Paroli, Chiara Gioia, Daniele Accapezzato   +2 more
doaj   +1 more source

Leptin May Promote Eosinophilic CRSwNP Progression by Enhancing Eosinophil Chemotaxis and Angiogenesis Under a Type 2 Inflammatory Milieu

International Forum of Allergy &Rhinology, EarlyView.
ABSTRACT Background Chronic rhinosinusitis with nasal polyp (CRSwNP) is a heterogeneous Type 2 inflammatory disease characterized by enhanced eosinophilic infiltration. Both innate and adaptive immunity are involved in the onset and progression of CRSwNP.
Yuki Sonoda, Yohei Sato, Yoshimasa Imoto, Mayumi Tamari, Shigeharu Fujieda   +4 more
wiley   +1 more source