{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,15]],"date-time":"2026-06-15T06:27:01Z","timestamp":1781504821530,"version":"3.54.1"},"reference-count":35,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2007,6,8]],"date-time":"2007-06-08T00:00:00Z","timestamp":1181260800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Cutan Pathol"],"published-print":{"date-parts":[[2007,10]]},"abstract":"<jats:p><jats:bold>Background:\u2002<\/jats:bold> Wegener\u2019s granulomatosis (WG), a systemic vasculitis, can be associated with cutaneous signs and symptoms before, during or after the diagnosis of systemic disease.<\/jats:p><jats:p><jats:bold>Methods:\u2002<\/jats:bold> We reviewed clinical and histologic features of cutaneous lesions from 17 patients with WG. The temporal relationship between development of cutaneous symptoms and onset of systemic disease was determined, and antineutrophil cytoplasmic antibody (ANCA) status of the patients was also established.<\/jats:p><jats:p><jats:bold>Results:\u2002<\/jats:bold> In six patients, systemic and cutaneous disease developed concurrently. In eight patients, cutaneous disease developed after patients received the diagnosis of systemic disease. In three patients, cutaneous disease preceded systemic disease. Cytoplasmic ANCA or proteinase\u20103\u2010ANCA [c\u2010ANCA\/proteinase 3 (PR3)\u2010ANCA] serologic test results were negative for one patient when cutaneous disease developed, and one patient had c\u2010ANCA\/PR3\u2010ANCA seroconversion a year before systemic disease developed. Histopathologic features of cutaneous WG were not limited to leukocytoclastic vasculitis; they also included acneiform perifollicular and dermal granulomatous inflammation and palisaded neutrophilic and granulomatous inflammation.<\/jats:p><jats:p><jats:bold>Conclusions:\u2002<\/jats:bold> Patients with WG can present initially with cutaneous symptoms. Histopathologic patterns vary, but leukocytoclastic vasculitis is most commonly noted. Patients with WG and skin lesions are likely to have positive c\u2010ANCA\/PR3\u2010ANCA serologic test results.<\/jats:p>","DOI":"10.1111\/j.1600-0560.2006.00699.x","type":"journal-article","created":{"date-parts":[[2007,6,8]],"date-time":"2007-06-08T11:45:45Z","timestamp":1181303145000},"page":"739-747","source":"Crossref","is-referenced-by-count":69,"title":["Cutaneous manifestations of Wegener\u2019s granulomatosis: a clinicopathologic study of 17 patients and correlation to antineutrophil cytoplasmic antibody status"],"prefix":"10.1111","volume":"34","author":[{"given":"Nneka I.","family":"Comfere","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nada C.","family":"Macaron","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lawrence 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