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作 者:Lina Pan Jingru Zhang Peng Li Chuanli Zhao Shaolei Zang Min Ji Fei Lu Jingjing Ye Chunqing Zhang Chunyan Ji
机构地区:[1]Department of Hematology,Qilu Hospital of Shandong University,Jinan,China.
出 处:《Emergency and Critical Care Medicine》2022年第4期233-238,共6页急危重症医学(英文)
基 金:the Shandong Provincial Natural Science Foundation(ZR2020MH119,ZR2020MH118);Distinguished Taishan Scholars in Climbing Plan(tspd20210321);National Nature Science Foundation of China(81400118,81700143);the horizontal subject of Shandong University(6010120072).
摘 要:A middle-aged man was diagnosed with myelodysplastic/myeloproliferative neoplasm-unclassifiable(MDS/MPN-U),with severe and extensive corticosteroid-resistant Sweet’s syndrome(SS)as the first manifestation,with evidence of clinical manifestations,pathological description,and laboratory evaluation.The skin lesions continued to spread despite treatment with systemic corticosteroids but were successfully treated with intravenous immunoglobulin(IVIG).
关 键 词:Case report Corticosteroid-resistant Intravenous immunoglobulin Myelodysplastic/myeloproliferative neoplasmunclassifiable Sweet’s syndrome
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