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慢性移植物抗宿主病相关浆膜炎和心包炎。

Chronic GvHD-associated serositis and pericarditis.

作者信息

Leonard J T, Newell L F, Meyers G, Hayes-Lattin B, Gajewski J, Heitner S, Nonas S, Allen B, Stentz A, Frires R, Maziarz R T, Holtan S G

机构信息

Department of Hematology & Medical Oncology, Blood & Marrow Transplant Program, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.

Department of Cardiology, Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA.

出版信息

Bone Marrow Transplant. 2015 Aug;50(8):1098-104. doi: 10.1038/bmt.2015.105. Epub 2015 May 11.

Abstract

Serositis is a rare manifestation of chronic GvHD (cGvHD). No risk factors or laboratory changes associated with this syndrome have been recognized to date, and outcomes have not been described in a large series. We searched our institutional database for patients undergoing allogeneic hematopoietic cell transplant identified as having serositis or pericarditis. Laboratory studies from prior to diagnosis, at diagnosis and post diagnosis of serositis, as well as outcomes from invasive procedures were included. Twenty patients met criteria for cGvHD-associated serositis, and all but three patients had a prior diagnosis of cGvHD. Fifteen were male, and the complication occurred in the setting of immunosuppressant taper in 12 cases. Ten patients required invasive interventions, including pericardial window or stripping. A significant increase in blood monocytes and decrease in serum albumin were identified at diagnosis compared with pre-diagnosis. Out of 20 patients, 17 were treated with steroids, with 12 demonstrating a complete response. These data suggest that cGvHD-associated serositis occurs mainly in the setting of treated as opposed to de novo cGvHD and biomarkers associated with the syndrome include a decrease in albumin and an increase in absolute monocyte count. Outcome data from larger series are required to better understand the optimal management of this rare complication.

摘要

浆膜炎是慢性移植物抗宿主病(cGvHD)的一种罕见表现。迄今为止,尚未发现与该综合征相关的危险因素或实验室变化,也没有对大量病例的预后进行描述。我们在机构数据库中搜索了接受异基因造血细胞移植且被确定患有浆膜炎或心包炎的患者。纳入了浆膜炎诊断前、诊断时和诊断后的实验室检查结果,以及侵入性操作的结果。20例患者符合cGvHD相关浆膜炎的标准,除3例患者外,其余均曾被诊断为cGvHD。15例为男性,12例并发症发生在免疫抑制剂减量过程中。10例患者需要进行侵入性干预,包括心包开窗或心包剥脱术。与诊断前相比,诊断时血液单核细胞显著增加,血清白蛋白降低。20例患者中,17例接受了类固醇治疗,12例显示完全缓解。这些数据表明,cGvHD相关浆膜炎主要发生在经治疗的情况下,而非新发cGvHD,与该综合征相关的生物标志物包括白蛋白降低和绝对单核细胞计数增加。需要更多病例系列的预后数据,以更好地了解这种罕见并发症的最佳管理方法。

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