{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:35:34Z","timestamp":1787841334191,"version":"build-2784847793"},"reference-count":11,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2014,4,1]],"date-time":"2014-04-01T00:00:00Z","timestamp":1396310400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2013,12,6]],"date-time":"2013-12-06T00:00:00Z","timestamp":1386288000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2014,4]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Paraneoplastic pemphigus is a rare dermatologic condition that can occur as a paraneoplastic manifestation of lymphoproliferative disorders, visceral malignancies, Castleman disease and thymomas. In a pediatric age group paraneoplastic pemphigus has a striking association with Castleman disease and has a particularly poor prognosis in this age group. We describe a case of paraneoplastic pemphigus associated with retroperitoneal hyaline vascular variant of Castleman disease with a fatal outcome despite aggressive management.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1016\/j.hemonc.2013.11.002","type":"journal-article","created":{"date-parts":[[2013,12,12]],"date-time":"2013-12-12T07:45:16Z","timestamp":1386834316000},"page":"93-96","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":12,"title":["Retroperitoneal Castlemans Disease associated with Paraneoplastic Pemphigus"],"prefix":"10.4103","volume":"7","author":[{"given":"Naseer A","family":"Choh","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Seema","family":"Qayoom","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Feroze","family":"Shaheen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rais A","family":"Malik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Irfan","family":"Rabbani","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tariq","family":"Gojwari","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"issue":"6","key":"10.1016\/j.hemonc.2013.11.002_b0005","doi-asserted-by":"crossref","first-page":"1793","DOI":"10.1148\/rg.316115502","article-title":"Castleman disease: the great mimic","volume":"31","author":"Bonekamp","year":"2011","journal-title":"Radiographics"},{"issue":"2","key":"10.1016\/j.hemonc.2013.11.002_b0010","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1148\/radiol.11100185","article-title":"Case 172: retroperitoneal Castleman disease (hyaline vascular type)","volume":"260","author":"Poole","year":"2011","journal-title":"Radiology"},{"issue":"4","key":"10.1016\/j.hemonc.2013.11.002_b0015","doi-asserted-by":"crossref","first-page":"e513","DOI":"10.1542\/peds.2004-0436","article-title":"Paraneoplastic autoimmune multiorgan syndrome (paraneoplastic pemphigus) in a child: case report and review of the literature","volume":"114","author":"Lane","year":"2004","journal-title":"Pediatrics"},{"key":"10.1016\/j.hemonc.2013.11.002_b0020","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1186\/1477-7819-5-45","article-title":"Retroperitoneal Castleman\u2019s tumor and paraneoplastic pemphigus: report of a case and review of the literature","volume":"5","author":"Menenakos","year":"2007","journal-title":"World J. 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