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The patient was refractory to conventional immunosuppressive therapy. Therefore, multiple devastating<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>lesions and disease activity in granulomatosis with polyangiitis (<jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content>) were controlled with infliximab. Later, rituximab was used with success to prevent recurrence of symptoms. The relationship of<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>with various autoimmune diseases is known; however,<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>in<jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content>has been only rarely reported. Biologic agents might prove to be effective in<jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">PG<\/jats:styled-content>patients who are refractory to standard immunosuppressive therapy.<\/jats:p>","DOI":"10.1111\/1756-185x.12274","type":"journal-article","created":{"date-parts":[[2014,1,27]],"date-time":"2014-01-27T11:37:33Z","timestamp":1390822653000},"page":"471-475","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":30,"title":["A case of granulomatosis with polyangiitis and pyoderma gangrenosum successfully treated with infliximab and rituximab"],"prefix":"10.1111","volume":"17","author":[{"given":"Salim","family":"Donmez","sequence":"first","affiliation":[{"name":"Department of Rheumatology Trakya University Medical Faculty Edirne Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Omer 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