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  1. 6801
    “…The various histological features including Bowman's capsule rupture, peri-glomerular granulomatous reaction, fibrinoid necrosis, and vasculitis were more common in anti-GBM disease and pauci-immune CrGN. …”
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    Etiological Spectrum and Clinical Features in 215 Patients of Crescentic Glomerulonephritis: Is it Different in India?
  2. 6802
    “…A significant correlation between chemerin level and five-factor score (FFS) was found (r = 0.320, p = 0.011), and resistin was correlated with both Birmingham vasculitis activity score and FFS (r = 0.256, p = 0.043 and r = 0.320, p = 0.011). …”
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    Serum adipokine profiles in patients with microscopic polyangiitis and granulomatosis with polyangiitis: An exploratory analysis
  3. 6803
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    Three cases of immunoglobulin G4-related respiratory disease with uncommon imaging findings
  4. 6804
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  5. 6805
    “…The main detectable histopathology lesions among the infected animals were orchitis (75%), mastitis in immature and lactating udder (66.66%), and necrotic hepatitis (77.77%), disseminated vasculitis (61.11), glomerulonephritis (55.55), myocardial degeneration (50%), and serous atrophy of coronary fats (38.88%), lymphadenitis (88.88%), necrosis and depleted lymphoid tissue of spleen (38.88%), necrotic myositis (77.77%), tracheitis (16.66%), and pneumonia (interstitial bronchopneumonia) (44.44%) besides intra-cytoplasmic inclusions bodies in skin (33.33%). …”
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    Prevalence, intensity, and impacts of non-cutaneous lesions of lumpy skin disease among some infected cattle flocks in Nile Delta governorates, Egypt
  6. 6806
    “…In 2 cases the dominant picture was urticarial vasculitis, possibly reflective of an Arthus type III immune complex action. …”
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    The histologic and molecular correlates of COVID-19 vaccine-induced changes in the skin
  7. 6807
    “…BACKGROUND: Behcet's disease (BD) is an autoimmune disease of systemic vasculitis with an unclear pathogenesis. Although western medicines remain the mainstay interventions, effectiveness and safety are significant challenges. …”
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    Effectiveness and Safety of Chinese Medicine Decoctions for Behcet's Disease: A Systematic Review and Meta-Analysis
  8. 6808
    “…BACKGROUND: Kawasaki disease (KD) is a systemic vasculitis that predominantly occurs in children, but the pathogenesis of KD remains unclear. …”
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    Identification of Key Genes and Underlying Mechanisms in Acute Kawasaki Disease Based on Bioinformatics Analysis
  9. 6809
    “…Behçet’s disease (BD) is a systemic autoinflammatory vasculitis. It occurs predominantly in Turkey but very rarely in Europe. …”
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    Behçet’s Disease in a Polish Patient: A Case Report
  10. 6810
    “…Hematoxylin and eosin staining of her back skin revealed abundant eosinophilic infiltrate around the vascular area of the shallow dermis layer, but no evidence of vasculitis and we diagnosed her as eosinophilic annular erythema (EAE). …”
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    Eosinophilic annular erythema showing eosinophil cytolytic ETosis successfully treated with benralizumab
  11. 6811
    por Khairwa, Anju
    Publicado 2021
    “…Data searched were PubMed, EMBASE, Google scholar, and Cochrane Database from inception to 31st January 2019 RESULTS: Total 49 studies (N=2480) were included: 21 studies (N=2309) of primary IgAN; 19 studies (N=21) of Secondary IgAN; four studies (N=133) of IgA vasculitis nephropathy (IgAVN); and five studies (N=17) of IgA dominant nephropathy (IgADN). …”
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    Indian scenario of IgA nephropathy: a systematic review and meta-analysis
  12. 6812
    “…Takayasu arteritis (TA) is a chronic inflammatory disease characterized by granulomatous vasculitis that predominantly manifests as panaortitis. …”
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    Takayasu Arteritis Mistaken for Epilepsy: A Case Presenting With Convulsive Syncope
  13. 6813
    “…OBJECTIVE: Kawasaki disease (KD) is a systemic vasculitis in childhood that can lead to coronary artery lesions (CALs). …”
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    Leucine-rich alpha-2-glycoprotein 1 and angiotensinogen as diagnostic biomarkers for Kawasaki disease
  14. 6814
    “…However, the cytokine storm induced by COVID-19 may trigger common post-viral glomerular disease such as IgA nephropathy, anti-GBM, and ANCA vasculitis that have also been described in COVID-19 patients. …”
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    Current Understanding of Clinical Manifestations of COVID-19 in Glomerular Disease
  15. 6815
    “…On correlating these findings with the gradient of the disease, livedo, vasculitis, exfoliation, and erythroderma were associated with severe disease, whereas perniosis and eruptive pseudoangioma were seen in mild illness. …”
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    An Observational Study of Mucocutaneous Manifestations among SARS-CoV-2 Patients from Three COVID-19 Dedicated Tertiary Care Centers
  16. 6816
    “…OBJECTIVES: GCA is a large vessel vasculitis (LVV) presenting with headache, jaw claudication, musculoskeletal and visual involvement. …”
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    Patient perceptions of health-related quality of life in giant cell arteritis: international development of a disease-specific patient-reported outcome measure
  17. 6817
    “…Kawasaki disease (KD) is an acute vasculitis of young children. A comparison of US hospitalization rates and epidemiologic features of KD in 2020 to those of precoronavirus disease years has yet to be reported. …”
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    Kawasaki Disease Hospitalizations in the United States 2016–2020: A Comparison of Before and During the Coronavirus Disease 2019 Era
  18. 6818
    “…However, there was a significant decrease in patients diagnosed with FMF, IgA vasculitis (IgAV), acute rheumatic fever (ARF), classic Kawasaki disease (KD), and macrophage activation syndrome (MAS) (all p < 0.05). …”
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    Impact of the COVID-19 pandemic on the frequency of the pediatric rheumatic diseases
  19. 6819
    “…The AAs/SAs showed a new signal of vasculitis at week 4 in three patients, with an IMT increase up to week 8. …”
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    Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
  20. 6820
    “…Patient: Male, 2-month-old Final Diagnosis: Kawasaki disease Symptoms: Bleeding and peeling lips • conjunctival injection • erythema of the palms and soles • erythematous (polymorphous) maculopapular rash • fever • nasal congestion Medication: — Clinical Procedure: Echocardiography • electrocardiogram Specialty: Pediatrics and Neonatology OBJECTIVE: Rare disease BACKGROUND: Kawasaki disease (KD) is an acute inflammatory vasculitis, which occurs mostly in childhood, predominantly between the ages of 6 months and 5 years. …”
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    A 2-Month-Old with Kawasaki Disease with Coronary Artery Dilation in the Pre-COVID-19 Era
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