2003
DOI: 10.1016/s0002-9343(03)00056-1
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Evidence of autoimmunity in chronic periaortitis: a prospective study

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Cited by 191 publications
(190 citation statements)
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“…A recent case-control study that compared inflammatory and noninflammatory abdominal aortic aneurysms showed that IAAAs are more (6). Likewise, in a recent study, we found that in 7 (44%) of 16 cases CP was associated with other autoimmune conditions, namely ANCA-positive renal disease and autoimmune tyroiditis (7). Finally, various case reports have described an association between CP and numerous autoimmune diseases including well-defined small-and medium-vessel vasculitis (Wegener's granulomatosis, polyarteritis nodosa, Henoch-Schoenlein purpura) (9 -11), unclassifiable "systemic vasculitis" (8,12), aortitis (13), or different types of immune-mediated glomerulonephritis (membranous, membrano-proliferative, and rapidly progressive glomerulonephritis) (18,19).…”
Section: Discussionsupporting
confidence: 61%
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“…A recent case-control study that compared inflammatory and noninflammatory abdominal aortic aneurysms showed that IAAAs are more (6). Likewise, in a recent study, we found that in 7 (44%) of 16 cases CP was associated with other autoimmune conditions, namely ANCA-positive renal disease and autoimmune tyroiditis (7). Finally, various case reports have described an association between CP and numerous autoimmune diseases including well-defined small-and medium-vessel vasculitis (Wegener's granulomatosis, polyarteritis nodosa, Henoch-Schoenlein purpura) (9 -11), unclassifiable "systemic vasculitis" (8,12), aortitis (13), or different types of immune-mediated glomerulonephritis (membranous, membrano-proliferative, and rapidly progressive glomerulonephritis) (18,19).…”
Section: Discussionsupporting
confidence: 61%
“…Finally, various case reports have described an association between CP and numerous autoimmune diseases including well-defined small-and medium-vessel vasculitis (Wegener's granulomatosis, polyarteritis nodosa, Henoch-Schoenlein purpura) (9 -11), unclassifiable "systemic vasculitis" (8,12), aortitis (13), or different types of immune-mediated glomerulonephritis (membranous, membrano-proliferative, and rapidly progressive glomerulonephritis) (18,19). Ankylosing spondylitis, a condition sometimes linked to ascending aortitis, has also been reported to be associated with CP (12,20,21), whereas the association with rheumatoid arthritis and systemic lupus erythematosus is uncommon (7,22). Finally, CP (particularly IRF) may frequently be associated with fibroinflammatory disorders affecting other organs (sclerosing cholangitis, mediastinal fibrosis, Riedel's and chronic autoimmune thyroiditis) (3,8,23), most of which are thought to have an autoimmune pathogenesis.…”
Section: Discussionmentioning
confidence: 99%
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“…Erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) level are frequently high, and in some cases patients are positive for autoantibodies (4). The diagnosis is made by means of computed tomography (CT) or magnetic resonance imaging (MRI), but a histologic examination of the retroperitoneal tissue is sometimes required.…”
Section: Introductionmentioning
confidence: 99%
“…Our patient demonstrated evidence of 2.3-cm abdominal aortic dilatation without a history of hypertension just over 1.5 years prior to presenting with associated RPF. Studies suggest that chronic periaortitis results from a local inflammatory reaction to antigens in the atherosclerotic plaques of the abdominal aorta (3,(21)(22)(23)(24)(25)(26). However, the presence of constitutional symptoms, high concentrations of acute-phase reactants, and frequent association with autoimmune diseases that involve other organs would seem to indicate that chronic periaortitis (including IRPF) may be a manifestation of a systemic autoimmune or inflammatory disease (3,22,23,27).…”
Section: Irpfmentioning
confidence: 99%