Tsokos G C, Balow J E, Spiegel R J, Magrath I T
Medicine (Baltimore). 1981 May;60(3):218-29. doi: 10.1097/00005792-198105000-00005.
The early metabolic events in 33 patients with non-Hodgkin lymphoma were analyzed in the present study. Twenty-three patients had Burkitt lymphoma, 3 had non-Burkitt undifferentiated lymphoma and 7 had lymphoblastic lymphoma. Eight patients developed azotemia prior to starting chemotherapy while five did so during the first treatment week. All the patients but two who developed azotemia had stage C or D disease. Serum LDH prior to chemotherapy correlated well with the stage of disease and predicted the serum levels of creatinine, uric acid and phosphorus in the post-treatment period. Surgical excision of the main tumor mass was associated with a low incidence of azotemia and other metabolic derangements. Hyperuricemia and occasionally obstruction were encountered as the causes of azotemia in the pre-treatment period. Hyperuricemia and/or hyperphosphatemia were presumed responsible for the development of azotemia in the post-chemotherapy period. Two patients were dialyzed for renal failure due to hyperuricemia and one for renal failure due to hyperphosphatemia which developed shortly after starting chemotherapy. The patterns of renal and metabolic disturbances observed during treatment of these patients were characterized by the following profiles: 1. Azotemia due to hyperuricemia prior to treatment. 2. Hyperuricemia without azotemia in the pre-treatment period with azotemia due to hyperphosphatemia in the post-treatment period. 3. Azotemia due to combined hyperphosphatemia and hyperuricemia developing gradually in post-treatment period. 4. Increased urine phosphorus excretion in both non-azotemic and azotemic patients.
本研究分析了33例非霍奇金淋巴瘤患者早期的代谢事件。23例患者为伯基特淋巴瘤,3例为非伯基特未分化淋巴瘤,7例为淋巴母细胞淋巴瘤。8例患者在开始化疗前出现氮质血症,5例在治疗第一周出现氮质血症。除2例出现氮质血症的患者外,所有患者均为C期或D期疾病。化疗前血清乳酸脱氢酶(LDH)与疾病分期密切相关,并可预测治疗后肌酐、尿酸和磷的血清水平。手术切除主要肿瘤肿块与氮质血症和其他代谢紊乱的低发生率相关。治疗前期,高尿酸血症和偶尔出现的梗阻是氮质血症的原因。化疗后,高尿酸血症和/或高磷血症被认为是氮质血症发生的原因。2例患者因高尿酸血症导致肾衰竭接受透析治疗,1例因化疗后不久出现的高磷血症导致肾衰竭接受透析治疗。在这些患者治疗期间观察到的肾脏和代谢紊乱模式具有以下特点:1. 治疗前因高尿酸血症导致氮质血症。2. 治疗前期无氮质血症的高尿酸血症,治疗后期因高磷血症导致氮质血症。3. 治疗后期因高磷血症和高尿酸血症合并逐渐出现氮质血症。4. 非氮质血症和氮质血症患者的尿磷排泄均增加。