IgA vasculitis
The profile and clinical outcomes of patients with renal involvement due to IgA vasculitis: is azathioprine a good option for treatment?
... to IgA vascu- litis, some studies have described a good clinical re- sponse and a reduction in IgA mesangial deposits, in post-treatment renal biopsy ...with IgA vasculitis, showed proteinuria ...
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Case Report Endoscopy and the management of IgA vasculitis: a clinical analysis of 261 pediatric immunoglobulin A (IgA) vasculitis cases with gastrointestinal involvement and endoscopic examinations of 69 patients
... of IgA vasculitis in pediatric patients, including clinical and endoscopic ...pediatric IgA vasculitis patients with gastrointestinal involvement who were admitted to our hospital between ...
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IgA vasculitis (Henoch – Schönlein Purpura) as the first manifestation of juvenile Systemic Lupus Erythematosus: Case-control study and systematic review
... with IgA vasculitis (HSP) + jSLE are older and predominantly girls, the direction of the bias should reduce the contrast between ...with IgA vasculitis (HSP) versus subjects with IgA ...
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A novel case of renal pathergy reaction in a Behçet’s disease patient complicated by IgA vasculitis
... Case presentation: A 46-year-old man who was diagnosed with IgA vasculitis (IgAV) at the age of 38 was treated with prednisolone and mizoribine. However, complications such as common carotid arteritis or ...
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Characterization of scrotal involvement in children and adolescents with IgA vasculitis
... with IgA vascu- litis followed at the Pediatric Rheumatology Department of our University Hospital during a 32-year period (January 1983 to December 2015) were retrospectively ...filled IgA ...
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Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch Schönlein purpura (IgA vasculitis)
... (IgA) vasculitis, is a leukocytoclastic vasculitis characterized by IgA-dominant immune deposits involving mainly the skin as well as other tissues ...this vasculitis is a palpable ...
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IgA vasculitis in adults: the performance of the EULAR/PRINTO/PRES classification criteria in adults
... cryoglobulinaemic vasculitis based on a history of recurrent episodes of purpura, nephritis and in one case a peripheral neuropathy, the presence of cryoglobulins, low C4, and disease evolution on follow- up, ...
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Association of HLA B*41:02 with Henoch Schönlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA DRB1 status
... systemic vasculitis in ...vessel vasculitis) has been reported ...(a vasculitis involving medium- sized blood vessels) is controversial, HLA-B*51 and HLA-B*44 have been proposed to be associated with ...
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Significance of histological crescent formation in patients with IgA vasculitis (Henoch-Schönlein purpura)-related nephritis: a cohort in the adult Chinese population
... Renal specimens with more than ten glomeruli were con- sidered adequate. Two pathologists, who were unaware of the clinical features, examined the specimens with light microscopy and immunofluorescence independently. ...
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Vaccination and Risk of Childhood IgA Vasculitis
... leukocytoclastic vasculitis or proliferative glomerulonephritis with predominant immunoglobulin A deposits, arthritis or arthralgia of acute onset, and renal involvement defined by proteinuria ...
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Intramuscular Hematoma as a Manifestation of IgA Vasculitis
... determined that his presentation was not consistent with in fl icted trauma. Because of the initial presentation of a rash consistent with IgAV and the risk of further organ involvement while diagnostic testing was ...
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Predicting gastrointestinal and renal involvement in adult IgA vasculitis
... Methods: The prospective study included histologically proven adult IgAV cases diagnosed between January 2013 and July 2019 at our secondary/tertiary rheumatology center. We evaluated the role of clinical and the ...
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Hypersensitivity Vasculitis with Leukocytoclastic Vasculitis Associated with Alpha-1-Proteinase Inhibitor
... conducted by the National Heart Lung and Blood institute (NHLBI) AATD Registry Group. The most frequent reported side effects include headache, dizziness, nausea, and dyspnea [5]. Although acute allergic reactions, ...
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HIV-1-Specific IgA Monoclonal Antibodies from an HIV-1 Vaccinee Mediate Galactosylceramide Blocking and Phagocytosis
... elicited IgA and its capacity to mediate antiviral ...HIV-1-specific IgA elicited by vaccination, we cloned HIV-1 envelope- specific IgA monoclonal antibodies (MAbs) by memory B cell cultures from ...
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Clinical Management of Uveitis in Systemic Rheumatic Autoimmune Diseases in Adults
... Acute recurrent unilateral anterior uveitis has been estimated to represent about one third of uveitis cases and, in about half of the cases, it is caused by SpA [3,5]. Acute non-recurrent unilateral uveitis corresponds ...
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Outcomes of patients admitted to intensive care units for acute manifestation of small vessel vasculitis: a multicenter, retrospective study
... Despite increased use, intensivists do not routinely pre- scribe immunosuppressive therapies for the management of severe vasculitis. In the ICU, their prescription in in- stances of multiple organ failure could ...
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Long term outcome of patients with ANCA associated vasculitis treated with plasma exchange: a retrospective, single centre study
... Renal Vasculitis (MEPEX) randomised trial, patients with severe renal vasculitis who received PLEX as adjunctive therapy had higher probability of dialysis independence at 1 year than patients treated with ...
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Eosinophilic Granulomatosis with Polyangiitis: Experiences in Korean Patients
... Eosinophilic granulomatosis with polyangiitis (EGPA) is one form of antineutrophil cytoplasmic antibody (ANCA)-associated vascu- litis. Identical to what has been called Churg-Strauss syndrome, EGPA exhibits both ...
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Cutaneous vasculitis: An etiological and clinicopathological study
... systemic vasculitis such as Polyarteritis nodosa (PAN), Wegener’s granulomatosis (WG), Churg Strauss syndrome (CSS) or secondary to drugs, infections or systemic diseases such as connective tissue disease (CTD) ...
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Myositis, Vasculitis, Hepatic Dysfunction in Adult-Onset Still's Disease
... with vasculitis, and elevated serum VEGF levels have been observed in Behc¸et’s disease, microscopic polyangiitis, polyarteritis nodosa, and giant cell arteritis ...
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