Results 101 to 110 of about 19,818 (230)
Crescentic glomerular nephritis associated with rheumatoid arthritis: a case report
Background Rheumatoid arthritis is a systemic disorder where clinically significant renal involvement is relatively common. However, crescentic glomerular nephritis is a rarely described entity among the rheumatoid nephropathies.
K. Balendran +2 more
doaj +1 more source
Associação de doença do anticorpo anti-membrana basal glomerular com dermatomiosite e psoríase: relato de caso [PDF]
CONTEXT: Anti-glomerular basement membrane (anti-GBM) antibody syndrome is characterized by deposition of anti-GBM antibodies on affected tissues, associated with glomerulonephritis and/or pulmonary involvement.
Buosi, Ana Letícia Pirozzi +5 more
core +2 more sources
ABSTRACT Severe protein C deficiency may present with recurrent multisystem thrombosis, including catastrophic mesenteric venous thrombosis in young adults. Early clinical suspicion, prompt imaging, and thrombophilia screening are essential for timely diagnosis and life‐saving intervention.
Akash Ahmed Alif +5 more
wiley +1 more source
Introduction: The side effects of antithyroid drugs are well known. Antineutrophil cytoplasmic antibody-associated vasculitis is a severe adverse reaction.
Gabriela Costa Andrade +4 more
doaj +1 more source
PR3-ANCA in Wegener's granulomatosis prime human mononuclear cells for enhanced activation via TLRs and NOD1/2 [PDF]
Background Anti-neutrophil cytoplasmic antibodies (ANCA) is autoantibodies characteristic of vasculitis diseases. A connection between ANCA and Wegener's granulomatosis was well established. The interaction of both ANCA phenotypes (PR3-ANCA and MPO-ANCA)
Iwashiro Atsushi +3 more
core +2 more sources
We describe a case of PLCH presenting as multiple obstructing bronchial lesions and pulmonary masses in a 36‐year‐old man. To our knowledge, this is the first report of PLCH presenting as bilateral hilar masses and airway obstructive lesions. ABSTRACT Pulmonary Langerhans cell histiocytosis is a rare lung disease, which was previously classified as ...
Jingyuan Fan +3 more
wiley +1 more source
Obinutuzumab treatment for antineutrophil cytoplasmic antibody-associated vasculitis
BackgroundAnti-CD20 therapy with rituximab serves as the cornerstone of both induction and maintenance treatment for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).
Chen Ye +26 more
doaj +1 more source
ABSTRACT Background/Aim Most patients with proteinuria are considered to have typical diabetic nephropathy (DN). However, when proteinuria occurs without diabetic retinopathy, with hematuria, or persists despite strict glycemic and blood pressure control, it is considered atypical for DN and warrants further evaluation for non‐DN via kidney biopsy ...
Shogo Kuwagata +16 more
wiley +1 more source
Nailfold videocapillaroscopy in antineutrophil cytoplasmic antibody–associated vasculitis
Objective Antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) is a group of illnesses that cause inflammation and alterations to small vessels in the body.
Megan M. Sullivan +4 more
doaj +1 more source
P-ANCA vasculitis in a patient with Alpha-1-Antitrypsin deficiency : a possible mechanism [PDF]
Antineutrophil cytoplasmic antibody (ANCA) testing plays a critical role in the diagnosis and classification of vasculitis. These antibodies are strongly associated with Wegener's granulomatosis, microscopic polyangiitis and Churg-Strauss syndrome ...
Tuffaha, Ahmad
core

