Barakat Salim, Abdallah Batoul, Finianos Antoine, Mahmasani Layal Al
Department of Internal Medicine, American University of Beirut Medical Centre, Beirut, Lebanon.
Department of Internal Medicine, Division of Hematology-Oncology, American University of Beirut Medical Center, Beirut, Lebanon.
Clin Med Insights Case Rep. 2022 Oct 19;15:11795476221129238. doi: 10.1177/11795476221129238. eCollection 2022.
Tumor lysis syndrome (TLS) is an oncologic emergency that is usually associated with hematologic malignancies either spontaneously or following early chemotherapy and is caused by massive tumor cell lysis. However, it has been rarely reported in solid tumors. We report a case of 25-year-old lady recently diagnosed with metastatic gastric adenocarcinoma who developed TLS after the fourth cycle of chemoimmunotherapy (FOLFOX plus Nivolumab). She presented with abdominal pain, decrease in oral intake and decreased urine output. Laboratory studies showed acute kidney injury with electrolyte disturbances and was diagnosed initially with autoimmune nephritis secondary to Nivolumab but was later found to have TLS and recovered after appropriate treatment. Soon after this complication, our patient was found to have disease progression on imaging which makes the incidence of TLS an indicator of disease progression.
肿瘤溶解综合征(TLS)是一种肿瘤急症,通常与血液系统恶性肿瘤自发相关,或在早期化疗后出现,由大量肿瘤细胞溶解引起。然而,实体瘤中鲜有报道。我们报告一例25岁女性,近期诊断为转移性胃腺癌,在接受第四周期化疗免疫治疗(FOLFOX加纳武单抗)后发生TLS。她出现腹痛、口服摄入量减少和尿量减少。实验室检查显示急性肾损伤伴电解质紊乱,最初诊断为纳武单抗继发的自身免疫性肾炎,但后来发现患有TLS,经适当治疗后康复。在这一并发症发生后不久,我们的患者在影像学检查中发现疾病进展,这使得TLS的发生率成为疾病进展的一个指标。