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  1. 6441
    “…Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. A genome-wide association study showed a correlation between ANCA-negative EGPA and variants of genes encoding proteins with intestinal barrier functions, suggesting that modifications of the mucosal layer and consequent gut dysbiosis might be involved in EGPA pathogenesis. …”
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    Gut Microbiota and Associated Mucosal Immune Response in Eosinophilic Granulomatosis with Polyangiitis (EGPA)
  2. 6442
    “…In addition to febrile pharyngitis and migratory polyarthritis in initial attacks, pericarditis was encountered in 1, valvulitis in 2, prolong PR interval in 3 and skin involvement in 2 patients with erythema marginatum and IgA vasculitis. All responded to antibiotics and nonsteroidal anti-inflammatory drugs therapy with normalized clinical and laboratory abnormalities, no new-onset carditis, and no recurrent disease during a long-term follow-up (3.8–19.8 years, 12.7 ± 5.4). …”
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    Acute rheumatic fever in adult patients
  3. 6443
    “…In addition, GCA patients lose anti-inflammatory Treg cells, promoting tissue-destructive granulomatous vasculitis. In summary, emerging data identify T cell aging as a risk factor for autoimmune disease and directly link TASPs to the breakdown of T cell tolerance and T-cell-induced tissue inflammation.…”
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    T-Cell Aging-Associated Phenotypes in Autoimmune Disease
  4. 6444
    “…We also address several additional mechanisms that may cause HPA axis dysfunction, including critical illness-related corticosteroid insufficiency, the direct cytopathic impacts of SARS-CoV-2 infection on the adrenals, pituitary, and hypothalamus, immune-mediated inflammations, small vessel vasculitis, microthrombotic events, the resistance of cortisol receptors, and impaired post-receptor signaling, as well as the dissociation of ACTH and cortisol regulation. …”
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    The Relationship between COVID-19 and Hypothalamic–Pituitary–Adrenal Axis: A Large Spectrum from Glucocorticoid Insufficiency to Excess—The CAPISCO International Expert Panel
  5. 6445
    “…The pathologies seen were in order of frequency: Infectious dermatoses (n=469) dominated by erysipelas in adults (n=302) and viral dermatoses in children (n=47); drug-induced skin reactions (n=160); inflammatory dermatoses (n=113) including erythroderma (n=36), urticaria (n=32), vasculitis (n=25), and erythema multiform (n=20); autoimmune bullous dermatoses (n=74); and physical skin diseases (n=27). …”
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    Dermatological emergencies: a Moroccan retrospective case series over a period of two years
  6. 6446
    “…The most frequent diagnostic categories included drug reaction (13.2%), leukocytoclastic vasculitis (8.5%), skin cancer (5.4%), graft‐vs‐host disease (3.5%), connective tissue disease (3.3%), and calciphylaxis (3.0%). …”
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    Diagnoses of hospitalized patients with skin abnormalities prompting biopsy by consulting dermatologists: A 3‐year review from a tertiary care center
  7. 6447
    “…Our results suggest that VTE in GPA is a recurrent co-morbidity, not always during active vasculitis, and more so in those with renal involvement and constitutional symptoms at the time of first VTE.…”
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    Recurrence rate of venous thromboembolic events in granulomatosis with polyangiitis
  8. 6448
    “…Periprosthetic tissues from 165 metal‐on‐metal hip revisions were examined for features of aseptic lymphocytic vasculitis associated lesions (ALVAL) as rated using two scoring systems as well as rankings for macrophage and lymphocyte numbers, intracellular wear debris and necrosis. …”
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    Semi‐quantitative histology confirms that the macrophage is the predominant cell type in metal‐on‐metal hip tissues
  9. 6449
    “…Immunoglobulin A vasculitis (IgAV) nephritis, also known as Henoch-Schönlein purpura nephritis (HSPN), is a condition in which small blood vessel inflammation and perivascular IgA deposition in the kidney caused by neutrophil activation, which more often leads to chronic kidney disease and accounts for 1%–2% of children with end-stage renal disease (ESRD). …”
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    Individualized medication based on pharmacogenomics and treatment progress in children with IgAV nephritis
  10. 6450
    “…Dysregulation of the CS has been associated with the development of several autoimmune disorders such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), ANCA-associated vasculitis, and autoimmune bullous dermatoses (AIBDs), where complement drives the inflammatory response in the effector phase. …”
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    Anaphylatoxins spark the flame in early autoimmunity
  11. 6451
    “…BACKGROUND: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis. Cardiac involvement is the major cause of morbidity and mortality in these patients. …”
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    A case report of myocarditis secondary to eosinophilic granulomatosis with polyangiitis
  12. 6452
    “…OBJECTIVE: Henoch–Schönlein purpura is a systemic vasculitis that mainly occurs in children. Renal impairment is a major complication of Henoch–Schönlein purpura, but there is no established predictive marker for renal involvement. …”
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    Risk factors for renal involvement in Henoch–Schönlein purpura
  13. 6453
    “…BACKGROUND: Henoch-Schönlein purpura (HSP) is an IgA-mediated small vessel vasculitis, typical of childhood. It’s a self-limiting disease and it affects different systems. …”
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    Henoch-Schönlein purpura following COVID-19 vaccine in a child: a case report
  14. 6454
    “…Renal biopsy did not reveal any immune-mediated glomerulonephritis or vasculitis, but hypertensive nephropathy was diagnosed. …”
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    A rare case of alveolar hemorrhage with hypertensive emergency
  15. 6455
    “…BACKGROUND: Kawasaki disease (KD) is an acute self-limiting febrile vasculitis that occurs during childhood and can cause coronary artery aneurysm (CAA). …”
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    ST-segment elevation myocardial infarction in Kawasaki disease: A case report and review of literature
  16. 6456
    “…In view of multiorgan involvement and absence of a microbiological diagnosis of tuberculosis, vasculitis was considered and he was treated with steroids. …”
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    DRESS syndrome due to first-line antitubercular therapy – A diagnostic imbroglio!
  17. 6457
    “…BACKGROUND: Kawasaki disease (KD) is a medium vessel vasculitis occurring in children, as yet of undetermined aetiology. …”
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    Unusual interventional treatment of a complex calcified coronary artery lesion in a child with Kawasaki disease: a case report
  18. 6458
    “…This case is reported to inform that bowel perforation due to ischemia or vasculitis may complicate the course of COVID-19 and, in cases of gastrointestinal symptoms, should be considered.…”
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    Small Intestine Perforation in a 69-Year-Old Man with COVID-19
  19. 6459
    “…Behçet’s syndrome (BS) is a chronic form of relapsing multisystem vasculitis, characterized by recurrent oral and genital ulcers. …”
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    Case report: Refractory intestinal Behçet’s syndrome successfully treated with tofacitinib: A report of four cases
  20. 6460
    “…The most common reactions were cutaneous small‐vessel vasculitis (19.2%), interface/lichenoid reactions (19.2%), psoriasis (15.4%), and acute urticaria (11.5%). …”
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    Cutaneous reactions post‐COVID‐19 vaccination. Case series and literature review
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