{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T02:09:16Z","timestamp":1777860556108,"version":"3.51.4"},"reference-count":15,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2022,4,2]],"date-time":"2022-04-02T00:00:00Z","timestamp":1648857600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,6,24]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:p>We had two cases of trisomy 8-positive myelodysplastic syndrome (MDS) with incomplete Beh\u00e7et\u2019s disease (BD) in which the remissions of both diseases were maintained by allogeneic stem cell transplantation (allo-SCT). Among MDS with BD patients, sometimes it is difficult to control the symptoms of BD with standard therapies such as corticosteroids and tumor necrosis factor (TNF) inhibitors. Although there should be careful consideration regarding indications for transplantation, our two cases, in which refractory BD was completely controlled by allo-SCT, suggest that allo-SCT can be one of the treatment options for higher-risk MDS with BD patients.<\/jats:p>","DOI":"10.1093\/mrcr\/rxac032","type":"journal-article","created":{"date-parts":[[2022,4,2]],"date-time":"2022-04-02T07:32:13Z","timestamp":1648884733000},"page":"273-277","source":"Crossref","is-referenced-by-count":4,"title":["Allogeneic stem cell transplantation for trisomy 8-positive myelodysplastic syndrome or myelodysplastic\/myeloproliferative disease with refractory Beh\u00e7et\u2019s disease: Case report and the review of literature"],"prefix":"10.1093","volume":"6","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3149-2584","authenticated-orcid":false,"given":"Takashi","family":"Onaka","sequence":"first","affiliation":[{"name":"Department of Hematology, Kokura Memor ial Hospital , Kitakyushu, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kazuhisa","family":"Nakano","sequence":"additional","affiliation":[{"name":"Department of Hematology, Kokura Memor ial Hospital , Kitakyushu, Japan"},{"name":"Department of Rheumatology, Kawasaki Medical School , Kurashiki, Japan"},{"name":"The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan , Ktakyushu, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuri","family":"Uemoto","sequence":"additional","affiliation":[{"name":"Department of Hematology, Kokura Memor ial Hospital , Kitakyushu, Japan"},{"name":"The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan , Ktakyushu, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naoto","family":"Miyakawa","sequence":"additional","affiliation":[{"name":"Department of Hematology, Kokura Memor ial 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