{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,15]],"date-time":"2026-10-15T01:50:50Z","timestamp":1792029050919,"version":"4.4.0"},"reference-count":20,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2021,1,1]],"date-time":"2021-01-01T00:00:00Z","timestamp":1609459200000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["SAGE Open Medical Case Reports"],"published-print":{"date-parts":[[2021,1]]},"abstract":"<jats:p> Thymoma-associated multiorgan autoimmunity disease can be seen in patients with thymomas and presents with features of graft versus host disease. Here, we report a case of a 52-year-old woman with a complex medical history including malignant thymoma, myasthenia gravis, Good\u2019s syndrome, and T cell large granular lymphocytic leukemia who presented with a diffuse pruritic rash ultimately found to be compatible with a cutaneous presentation of thymoma-associated multiorgan autoimmunity disease. The eruption heralded the recurrence of the malignant thymoma and the rash was ultimately found to be resistant to a multitude of therapies except for oral corticosteroids. <\/jats:p>","DOI":"10.1177\/2050313x211055928","type":"journal-article","created":{"date-parts":[[2021,10,29]],"date-time":"2021-10-29T05:51:45Z","timestamp":1635486705000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":10,"title":["Thymoma-associated multiorgan autoimmunity with cutaneous only presentation: A case report"],"prefix":"10.1177","volume":"9","author":[{"given":"Solomon","family":"Bendayan","sequence":"first","affiliation":[{"name":"Faculty of Medicine, McGill University, Montreal, QC, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4531-6012","authenticated-orcid":false,"given":"Roxana","family":"Mititelu","sequence":"additional","affiliation":[{"name":"Division of Dermatology, McGill University Health Centre, Montreal, QC, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Margaret","family":"Elizabeth Redpath","sequence":"additional","affiliation":[{"name":"Department of Pathology, McGill University, Montreal, QC, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robin","family":"Billick","sequence":"additional","affiliation":[{"name":"Division of Dermatology, Jewish General Hospital, Montreal, QC, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2021,10,28]]},"reference":[{"key":"bibr1-2050313X211055928","doi-asserted-by":"publisher","DOI":"10.1016\/j.autrev.2015.09.005"},{"key":"bibr2-2050313X211055928","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2007.02.027"},{"issue":"6","key":"bibr3-2050313X211055928","first-page":"818","volume":"96","author":"Muramatsu K","year":"2016","journal-title":"Acta Derm 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