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转移性前列腺腺癌初治时的自发性肿瘤溶解综合征:一个不寻常的病例

Treatment-naïve spontaneous tumor lysis syndrome in metastatic prostate adenocarcinoma: An unusual suspect.

作者信息

Ignaszewski Maya, Kohlitz Patrick

机构信息

Department of Medicine, SUNY Upstate Medical University, Syracuse, NY, United States.

出版信息

Am J Emerg Med. 2017 Sep;35(9):1384.e1-1384.e2. doi: 10.1016/j.ajem.2017.05.044. Epub 2017 May 26.

Abstract

Tumor lysis syndrome (TLS) is a potentially fatal condition defined both by laboratory and clinical criteria. It is caused by the catabolism of tumor cells which leads to considerable release and elevated levels of phosphate, potassium and uric acid in the bloodstream. These electrolyte derangements predispose patients to renal tubule uric acid precipitation, acute kidney injury, arrhythmias, neuromuscular irritability and even seizures. Although this phenomenon is well described with hematological malignancies, it is also known to occur among solid tumors. We present a rare case of treatment-naïve spontaneous TLS that occurred in a 69-year-old male with metastatic prostate adenocarcinoma with hyperkalemia, hyperuricemia, hyperphosphatemia, hypocalcemia, elevated liver enzymes, AKI and hemodynamic instability. Despite our best resuscitative efforts with intravenous hydration, electrolyte monitoring, Rasburicase and renal replacement therapy, the patient continued to decline, was made comfort care and expired shortly thereafter. Physicians encountering patients with the above presentation must entertain a diagnosis of TLS despite its rarity in solid tumors, as early diagnosis leads to timely treatment, thereby maximizing patients' chances at survival.

摘要

肿瘤溶解综合征(TLS)是一种由实验室和临床标准定义的潜在致命病症。它由肿瘤细胞的分解代谢引起,导致血液中磷酸盐、钾和尿酸大量释放并水平升高。这些电解质紊乱使患者易发生肾小管尿酸沉淀、急性肾损伤、心律失常、神经肌肉兴奋性增加甚至癫痫发作。尽管这种现象在血液系统恶性肿瘤中已有充分描述,但在实体瘤中也会发生。我们报告一例罕见的未经治疗的自发性TLS病例,该病例发生在一名69岁患有转移性前列腺腺癌的男性患者身上,伴有高钾血症、高尿酸血症、高磷血症、低钙血症、肝酶升高、急性肾损伤和血流动力学不稳定。尽管我们通过静脉补液、电解质监测、拉布立酶和肾脏替代治疗尽了最大的复苏努力,但患者病情仍持续恶化,接受了舒适护理,此后不久死亡。遇到上述表现患者的医生,尽管TLS在实体瘤中罕见,但必须考虑其诊断,因为早期诊断可导致及时治疗,从而最大程度提高患者的生存机会。

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