ANCA‐associated optic neuropathy
Antineutrophil autoantibodies (ANCAs) directed against either antiproteinase3 (anti‐PR3) or myeloperoxidase (anti‐MPO) are associated with a small vessel vasculitis in which the characteristic feature is a focal necrotizing damage of capillaries, venules and arterioles. The ANCA‐associated vasculiti...
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| Veröffentlicht in: | Acta ophthalmologica (Oxford, England) England), 2019-12, Vol.97 (S263), p.n/a |
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| container_title | Acta ophthalmologica (Oxford, England) |
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| creator | Kawasaki, Aki |
| description | Antineutrophil autoantibodies (ANCAs) directed against either antiproteinase3 (anti‐PR3) or myeloperoxidase (anti‐MPO) are associated with a small vessel vasculitis in which the characteristic feature is a focal necrotizing damage of capillaries, venules and arterioles. The ANCA‐associated vasculitic syndromes are; granulomatosis with polyangiitis (formerly know as Wegener’s granulomatosis), microscopic polyangiitis, Churg‐Strauss syndrome and idiopathic necrotizing crescentic glomerulonephritis. Ocular and orbital manifestations may be a presenting manifestation of Wegener’s granulomatosis, in particular optic perineuritis. This presentation will review ANCA‐associated optic perineuritis and how it is distinguished from idiopathic optic perineuritis. |
| doi_str_mv | 10.1111/j.1755-3768.2019.8150 |
| format | Article |
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The ANCA‐associated vasculitic syndromes are; granulomatosis with polyangiitis (formerly know as Wegener’s granulomatosis), microscopic polyangiitis, Churg‐Strauss syndrome and idiopathic necrotizing crescentic glomerulonephritis. Ocular and orbital manifestations may be a presenting manifestation of Wegener’s granulomatosis, in particular optic perineuritis. This presentation will review ANCA‐associated optic perineuritis and how it is distinguished from idiopathic optic perineuritis.</description><identifier>ISSN: 1755-375X</identifier><identifier>EISSN: 1755-3768</identifier><identifier>DOI: 10.1111/j.1755-3768.2019.8150</identifier><language>eng</language><publisher>Malden: Wiley Subscription Services, Inc</publisher><subject>Antineutrophil cytoplasmic antibodies ; Arterioles ; Autoantibodies ; Capillaries ; Churg-Strauss syndrome ; Glomerulonephritis ; Granulomatosis ; Inflammatory diseases ; Optic neuropathy ; Peroxidase ; Vasculitis ; Vein & artery diseases</subject><ispartof>Acta ophthalmologica (Oxford, England), 2019-12, Vol.97 (S263), p.n/a</ispartof><rights>2019 The Authors Acta Ophthalmologica © 2019 Acta Ophthalmologica Scandinavica Foundation</rights><rights>Copyright © 2019 Acta Ophthalmologica Scandinavica Foundation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1755-3768.2019.8150$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1413,1429,27906,27907,45557,46815</link.rule.ids></links><search><creatorcontrib>Kawasaki, Aki</creatorcontrib><title>ANCA‐associated optic neuropathy</title><title>Acta ophthalmologica (Oxford, England)</title><description>Antineutrophil autoantibodies (ANCAs) directed against either antiproteinase3 (anti‐PR3) or myeloperoxidase (anti‐MPO) are associated with a small vessel vasculitis in which the characteristic feature is a focal necrotizing damage of capillaries, venules and arterioles. The ANCA‐associated vasculitic syndromes are; granulomatosis with polyangiitis (formerly know as Wegener’s granulomatosis), microscopic polyangiitis, Churg‐Strauss syndrome and idiopathic necrotizing crescentic glomerulonephritis. Ocular and orbital manifestations may be a presenting manifestation of Wegener’s granulomatosis, in particular optic perineuritis. This presentation will review ANCA‐associated optic perineuritis and how it is distinguished from idiopathic optic perineuritis.</description><subject>Antineutrophil cytoplasmic antibodies</subject><subject>Arterioles</subject><subject>Autoantibodies</subject><subject>Capillaries</subject><subject>Churg-Strauss syndrome</subject><subject>Glomerulonephritis</subject><subject>Granulomatosis</subject><subject>Inflammatory diseases</subject><subject>Optic neuropathy</subject><subject>Peroxidase</subject><subject>Vasculitis</subject><subject>Vein & artery diseases</subject><issn>1755-375X</issn><issn>1755-3768</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqNkM9KxDAQxoMouK4-grDouXXyt6m3UlwVFvfgHryFkKTYsm5q0iJ78xF8Rp_E1sqencsMw_eb4fsQusSQ4qFumhRnnCc0EzIlgPNUYg5HaHbYHh9m_nKKzmJsAAQWgs3QVfFUFt-fXzpGb2rdObvwbVebxc71wbe6e92fo5NKb6O7-OtztFnebcqHZLW-fyyLVWIw4ZDk0kLGrXVGaAcsy11eGQIEW-4YqSQFBhxzQjlIYZkQQK20ROrcMCeBztH1dLYN_r13sVON78Nu-KgIJZJmFOdiUPFJZYKPMbhKtaF-02GvMKgxDdWo0asafasxDTWmMXC3E_dRb93-f5Aq1s-_8A_YoGIG</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Kawasaki, Aki</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>201912</creationdate><title>ANCA‐associated optic neuropathy</title><author>Kawasaki, Aki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1250-98d075ddec6ae0479e9fc2021d5e42f83040515235086d46603d8d28a9c4e803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antineutrophil cytoplasmic antibodies</topic><topic>Arterioles</topic><topic>Autoantibodies</topic><topic>Capillaries</topic><topic>Churg-Strauss syndrome</topic><topic>Glomerulonephritis</topic><topic>Granulomatosis</topic><topic>Inflammatory diseases</topic><topic>Optic neuropathy</topic><topic>Peroxidase</topic><topic>Vasculitis</topic><topic>Vein & artery diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawasaki, Aki</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Acta ophthalmologica (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawasaki, Aki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ANCA‐associated optic neuropathy</atitle><jtitle>Acta ophthalmologica (Oxford, England)</jtitle><date>2019-12</date><risdate>2019</risdate><volume>97</volume><issue>S263</issue><epage>n/a</epage><issn>1755-375X</issn><eissn>1755-3768</eissn><abstract>Antineutrophil autoantibodies (ANCAs) directed against either antiproteinase3 (anti‐PR3) or myeloperoxidase (anti‐MPO) are associated with a small vessel vasculitis in which the characteristic feature is a focal necrotizing damage of capillaries, venules and arterioles. The ANCA‐associated vasculitic syndromes are; granulomatosis with polyangiitis (formerly know as Wegener’s granulomatosis), microscopic polyangiitis, Churg‐Strauss syndrome and idiopathic necrotizing crescentic glomerulonephritis. Ocular and orbital manifestations may be a presenting manifestation of Wegener’s granulomatosis, in particular optic perineuritis. This presentation will review ANCA‐associated optic perineuritis and how it is distinguished from idiopathic optic perineuritis.</abstract><cop>Malden</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/j.1755-3768.2019.8150</doi><tpages>1</tpages></addata></record> |
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| identifier | ISSN: 1755-375X |
| ispartof | Acta ophthalmologica (Oxford, England), 2019-12, Vol.97 (S263), p.n/a |
| issn | 1755-375X 1755-3768 |
| language | eng |
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| source | Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content |
| subjects | Antineutrophil cytoplasmic antibodies Arterioles Autoantibodies Capillaries Churg-Strauss syndrome Glomerulonephritis Granulomatosis Inflammatory diseases Optic neuropathy Peroxidase Vasculitis Vein & artery diseases |
| title | ANCA‐associated optic neuropathy |
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