利妥昔单抗治疗淋巴瘤引起的毛细血管渗漏综合征

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摘要

毛细血管渗漏综合征(CLS)的特征是血浆外渗至间质,导致低血压、无血、血浓缩和低白蛋白血症。最初在克拉克森病(系统性毛细血管渗漏综合征,SCLS)中报道,CLS已在多种疾病中观察到,最常见的是败血症。在肿瘤学中,慢性淋巴细胞白血病通常是治疗的并发症,而不是恶性肿瘤。在本病例研究中,我们记录了利妥昔单抗与多药化疗方案(EPOCH-R)联合使用时cls的临床表现、实验室特征和放射学表现。区分药物诱导的cls与败血症具有相同的临床特征,这对于避免进一步暴露于可能对患者致命的利妥昔单抗非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Capillary leak syndrome (CLS) from rituximab therapy of lymphoma
Capillary Leak Syndome (CLS) is characterized by plasma extravasation into the interstitium with resultant hypotension, anasarca, hemoconcentration, and hypoalbuminemia in the absence of albuminuria. Initially reported in Clarkson’s disease (systemic capillary leak syndrome, SCLS), CLS has been observed in multiple disease settings, the most common being sepsis. In Oncology, CLS has been reported more often as a complication from therapy, and less often from malignancy. In this case study, we documented clinical manifestation, laboratory features and radiological findings of CLS from rituximab therapy when employed in combination with a multi-agent chemotherapy regimen (EPOCH-R). Differentiating drug-induced CLS from sepsis, which presents with the same clinical features, is important in avoiding further exposure to rituximab, which could be fatal to the patient.
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