Tomlinson G C, Solberg L A
Cancer. 1984 Apr 15;53(8):1783-5. doi: 10.1002/1097-0142(19840415)53:8<1783::aid-cncr2820530829>3.0.co;2-f.
The acute tumor lysis syndrome occurs rarely in nonhematologic malignancies. This patient, a 34-year-old woman with metastatic medulloblastoma, was receiving palliative radiotherapy for a rapidly expanding abdominopelvic mass. After a total of 300 rad, the patient developed the biochemical hallmarks of the acute tumor lysis syndrome, hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. This was complicated by oliguria from hyperuricemic acute renal failure. The patient responded well to hydration, alkaline diuresis, phosphate and potassium binders, and allopurinol. The potential for acute tumor lysis syndrome should be anticipated when treating metastatic medulloblastoma.
急性肿瘤溶解综合征在非血液系统恶性肿瘤中很少见。该患者为一名34岁患有转移性髓母细胞瘤的女性,因迅速增大的腹盆腔肿块正在接受姑息性放疗。在总共接受300拉德放疗后,患者出现了急性肿瘤溶解综合征的生化特征,即高尿酸血症、高钾血症、高磷血症和低钙血症。这又因高尿酸血症性急性肾衰竭导致的少尿而复杂化。患者对补液、碱性利尿、磷酸盐和钾结合剂以及别嘌醇反应良好。在治疗转移性髓母细胞瘤时应预见到急性肿瘤溶解综合征的可能性。