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异基因造血干细胞移植后抗利尿激素分泌异常综合征(SIADH)的早期发作:病例报告及文献综述

Early onset of syndrome of inappropriate antidiuretic hormone secretion (SIADH) after allogeneic haematopoietic stem cell transplantation: case report and review of the literature.

作者信息

Wei J, Xiao Y, Yu X, Zhou J, Zhang Y

机构信息

Department of Haematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Int Med Res. 2010 Mar-Apr;38(2):705-10. doi: 10.1177/147323001003800235.

Abstract

Severe hyponatraemia and syndrome of inappropriate antidiuretic hormone secretion (SIADH) is a rare but fatal complication following stem cell transplantation (SCT). This case report details a patient with early-onset SIADH after allogeneic haematopoietic SCT (allo-HSCT) and reviews the literature on risk factors for the development of this condition. The patient, who had chronic myelogenous leukaemia, developed acute graft-versus-host disease (GVHD) on day 5 after allo-HSCT, which was relieved promptly by steroids. On day 18, he presented with hyponatraemia, which was refractory. Despite intensive restriction of fluid and administration of hypertonic saline, his condition worsened and he died of multiple systemic organ dysfunction. A review of the literature reveals that early-onset SIADH following SCT is insidious, but progresses rapidly. The severity of the disorder is underestimated because of the non-specific clinical features and the lack of effective treatment. Myeloablative conditioning and acute GVHD are two major important predisposing factors in SIADH.

摘要

严重低钠血症和抗利尿激素分泌不当综合征(SIADH)是干细胞移植(SCT)后一种罕见但致命的并发症。本病例报告详细介绍了一名异基因造血干细胞移植(allo-HSCT)后早期发生SIADH的患者,并回顾了关于该病症发生风险因素的文献。该患者患有慢性粒细胞白血病,在allo-HSCT后第5天发生急性移植物抗宿主病(GVHD),经类固醇治疗后迅速缓解。第18天,他出现低钠血症,且难以纠正。尽管严格限制液体摄入并给予高渗盐水治疗,但其病情仍恶化,最终死于多系统器官功能障碍。文献回顾显示,SCT后早期发生的SIADH隐匿,但进展迅速。由于临床特征不具特异性且缺乏有效治疗方法,该病症的严重程度被低估。清髓性预处理和急性GVHD是SIADH的两个主要重要诱发因素。

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