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纳武单抗引起的全身性毛细血管渗漏综合征是一种极其罕见的、危及生命的晚期毒性现象及静脉注射免疫球蛋白的疗效。

Nivolumab-induced systemic capillary leak syndrome as an ultra rare life-threatening phenomenon of late toxicity and intravenous immunoglobulin efficacy.

作者信息

Polishchuk Ilya, Yakobson Alexander, Zemel Melanie, A Sharb Adam, Shalata Walid, Rosenberg Eli, A Kian Tawfeek, Alguayn Farouq, Peled Nir, Rouvinov Keren, Alguayn Wafeek, Kian Waleed

机构信息

Internal Medicine Ward, Soroka Medical Center & Ben-Gurion University, Beer-Sheva, Israel.

The Legacy Heritage Oncology Center & Dr Larry Norton Institute, Soroka Medical Center & Ben-Gurion University, Beer-Sheva, Israel.

出版信息

Immunotherapy. 2021 Jul;13(10):807-811. doi: 10.2217/imt-2020-0335. Epub 2021 May 9.

Abstract

Systemic capillary leak syndrome (SCLS) is a life-threatening disease. It is characterized by severe capillary hyperpermeability to proteins resulting in hemoconcentration, hypoalbuminemia and hypovolemic shock. Its treatment remains supportive, and the prognosis is generally poor. We report on a 51-year old male with melanoma treated with nivolumab for 1 year. 1 month following the completion of the treatment, the patient presented with signs of hypovolemic shock, anasarca, hemoconcentration and hypoalbuminemia. After excluding other diseases, a diagnosis of nivolumab-induced systemic capillary leak syndrome was made. A high dose of intravenous steroid therapy was promptly initiated without any significant clinical improvement. Intravenous immunoglobulin therapy was then administered with normalization of blood pressure, hemoconcentration and complete resolution of anasarca. Intravenous immunoglobulin should be considered a first-line treatment option for this rare phenomenon.

摘要

系统性毛细血管渗漏综合征(SCLS)是一种危及生命的疾病。其特征是毛细血管对蛋白质的通透性严重增加,导致血液浓缩、低白蛋白血症和低血容量性休克。其治疗仍以支持治疗为主,预后通常较差。我们报告一例51岁男性黑色素瘤患者,接受纳武单抗治疗1年。治疗结束1个月后,患者出现低血容量性休克、全身性水肿、血液浓缩和低白蛋白血症的症状。排除其他疾病后,诊断为纳武单抗诱导的系统性毛细血管渗漏综合征。立即开始大剂量静脉类固醇治疗,但临床症状无明显改善。随后给予静脉注射免疫球蛋白治疗,血压恢复正常,血液浓缩情况改善,全身性水肿完全消退。对于这种罕见现象,静脉注射免疫球蛋白应被视为一线治疗选择。

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