{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,31]],"date-time":"2026-07-31T23:11:23Z","timestamp":1785539483490,"version":"3.56.0"},"reference-count":18,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2017,8,8]],"date-time":"2017-08-08T00:00:00Z","timestamp":1502150400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J of Rheum Dis"],"published-print":{"date-parts":[[2018,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objective<\/jats:title><jats:p>To describe the features of exceptional coexisting Takayasu arteritis (<jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>) and sarcoidosis, two conditions of unknown cause associated with a common immunologic pattern.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We report seven cases of concomitant sarcoidosis\u2010Takayasu or Takayasu\u2010like vasculitis, observed in two referral centers between 1995 and 2015.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>All patients were female. The mean age at sarcoidosis diagnosis and <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> diagnosis was 36 and 37\u00a0years, respectively. Sarcoidosis occurred in 86% of cases before or together with <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>. Sarcoidosis always had a classic expression except for one renal localization. Sarcoidosis was not severe and mostly non\u2010treated (86%). In all cases of <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>, supra\u2010aortic arteries were involved; in only two <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> cases a more diffuse inflammatory arterial involvement was noted. In one case, Takayasu arteritis occurred despite immunosuppressive therapy given for sarcoidosis. All patients received for <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> a treatment with corticosteroids associated with methotrexate (four cases), infliximab (one case) or tocilizumab (one case). After a mean follow\u2010up of 89\u00a0months, <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> always improved and no death was observed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> stands as pathology associated with sarcoidosis. <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> occurred in three cases among 50. When sarcoidosis preceded <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>, a recovery of sarcoidosis was achieved mostly without treatment. <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> is a prognostic and therapeutic factor. Immunosuppressive treatment, including steroids, led to a good prognosis for <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> as well as for sarcoidosis.<\/jats:p><\/jats:sec>","DOI":"10.1111\/1756-185x.13137","type":"journal-article","created":{"date-parts":[[2017,8,9]],"date-time":"2017-08-09T02:46:43Z","timestamp":1502246803000},"page":"740-745","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":22,"title":["Sarcoidosis with Takayasu arteritis: a model of overlapping granulomatosis. A report of seven cases and literature review"],"prefix":"10.1111","volume":"21","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2821-6626","authenticated-orcid":false,"given":"Catherine","family":"Chapelon\u2010Abric","sequence":"first","affiliation":[{"name":"Department of Internal Medicine and Clinical Immunology Groupe Hospitalier Piti\u00e9\u2010Salp\u00eatri\u00e8re AP\u2010HP Paris France"},{"name":"Sorbonne Universit\u00e9s UPMC Univ Paris 06 UMR 7211 and Inflammation\u2010Immunopathology\u2010Biotherapy Department (DHU i2B) Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Saadoun","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine and Clinical Immunology Groupe Hospitalier Piti\u00e9\u2010Salp\u00eatri\u00e8re AP\u2010HP Paris France"},{"name":"Sorbonne Universit\u00e9s UPMC Univ Paris 06 UMR 7211 and Inflammation\u2010Immunopathology\u2010Biotherapy Department (DHU i2B) Paris 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