Use of Plasmapheresis and Immunosuppressants to Treat Diffuse Alveolar Hemorrhage in a Patient with Granulomatosis with Polyangiitis. [PDF]
, 2019 Granulomatosis with polyangiitis (GPA) is a systemic granulomatous inflammatory disease characterized by small-to-medium vessel vasculitis due to Central Anti-Neutrophil Cytoplasmic Antibody (C-ANCA).
Sattar, Yasar +4 more
core +1 more source
Inflammatory bowel disease-specific autoantibodies in HLA-B27-associated spondyloarthropathies: Increased prevalence of ASCA and pANCA [PDF]
, 2004 Aims: An association between inflammatory bowel disease (IBD) and spondyloarthropathies (SpA) has repeatedly been reported. The aim of the present study was to investigate whether serologic markers of IBD, e. g.
Brumberger, V. +7 more
core +1 more source
Intracerebral haemorrhage in a dog with steroid-responsive meningitis arteritis [PDF]
, 2017 A one-year and six-month-old female neutered Boxer dog was presented with a four-day history of pyrexia, lethargy and neck pain. An intracerebral haemorrhage and a mediastinal mass were identified.
Brocal, Josep +3 more
core +1 more source
Hospital-onset IgA vasculitis triggered by infectious endocarditis
IDCases, 2023 This is a case of IgA vasculitis developed in the hospital during treatment of infective endocarditis. When purpura appears in a patient under IE treatment, we should consider IgA vasculitis as a differential diagnosis and check renal function.
Kento Furuya, Naoya Itoh
doaj
Iron Deficiency Anemia: An Unexpected Cause of an Acute Occipital Lobe Stroke in an Otherwise Healthy Young Woman [PDF]
, 2020 A 29-year-old caucasian woman who presented to the hospital with an acute onset of right eye visual disturbance and headache was found to have an acute left occipital lobe infarction.
Nace, Travis C +3 more
core +1 more source
Autoantibodies in systemic vasculitis [PDF]
, 2015 Systemic vas culitis is a heterogeneous group of disorders characterized by inflammation and necrosis in the vessel wall. the diagnosis of a systemic vasculitis is challenging, because patients usually present a broad spectrum of manifestations that vary
Souza, Alexandre Wagner Silva de
core +3 more sources
Acute pancreatitis in IgA vasculitis
Pediatria i Medycyna Rodzinna, 2021 IgA vasculitis, also known as the Henoch–Schönlein purpura, is the most common systemic vasculitis in children. Inflammation most often involves small blood vessels of the skin, joints, kidneys and the gastrointestinal tract, but other organs may also be involved. Acute pancreatitis is a rare clinical manifestation of IgA vasculitis.
Krzysztof Zeman +2 more
openaire +2 more sources
Microbial risk factors of cardiovascular and cerebrovascular diseases: potential therapeutic options [PDF]
, 2008 Infection and inflammation may have a crucial role in the pathogenesis of atherosclerosis. This hypothesis is supported by an increasing number of reports on the interaction between chronic infection, inflammation, and atherogenesis.
Abbas, M.A. +6 more
core +1 more source
IgA vasculitis in an adult diabetic male with rapidly progressive glomerulonephritis: A case study
Journal of Acute DiseaseRationale: IgA vasculitis or Henoch-Schonlein purpura is an immune complex mediated small vessel vasculitis characterized by clinical triad of arthritis, palpable purpura and gastrointestinal symptoms.
Varsha Luthra +4 more
doaj +1 more source
COVID19‐Related Onset and Relapses of Juvenile Systemic Lupus Erythematosus‐Like Disease
Journal of Paediatrics and Child Health, EarlyView.
Chiara Cannata +3 more
wiley +1 more source