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一名重型再生障碍性贫血患者在接受非亲缘骨髓移植后出现以横贯性脊髓炎、伊文氏综合征和肺部浸润为特征的免疫综合征。

An immunological syndrome featuring transverse myelitis, Evans syndrome and pulmonary infiltrates after unrelated bone marrow transplant in a patient with severe aplastic anemia.

作者信息

Richard S, Fruchtman S, Scigliano E, Skerrett D, Najfeld V, Isola L

机构信息

Department of Medicine, Mount Sinai Medical Center, New York, NY 10029, USA.

出版信息

Bone Marrow Transplant. 2000 Dec;26(11):1225-8. doi: 10.1038/sj.bmt.1702677.

Abstract

A patient with severe aplastic anemia underwent a matched unrelated bone marrow transplant, following which he developed a complex autoimmune syndrome. This featured transverse myelitis, immune mediated Coombs positive hemolytic anemia and immune thrombocytopenia (Evans syndrome), pulmonary infiltrates, eosinophilia, muscle pains and cramps and lichenoid dermatitis all of which may represent manifestations of graft-versus-host disease as they showed response to immunosuppression. Thus, although immune-mediated cytopenias after an allogeneic bone marrow transplant are rare, they should be considered as a possible cause of cytopenia in post-transplant patients.

摘要

一名严重再生障碍性贫血患者接受了匹配的无关供者骨髓移植,随后出现了一种复杂的自身免疫综合征。其特征包括横贯性脊髓炎、免疫介导的库姆斯试验阳性溶血性贫血和免疫性血小板减少症(伊文斯综合征)、肺部浸润、嗜酸性粒细胞增多、肌肉疼痛和痉挛以及苔藓样皮炎,所有这些都可能是移植物抗宿主病的表现,因为它们对免疫抑制有反应。因此,尽管异基因骨髓移植后免疫介导的血细胞减少症很少见,但在移植后患者中应将其视为血细胞减少的可能原因。

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