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首页> 外文期刊>Journal of nephrology. >Acute spontaneous tumor lysis presenting with hyperuricemic acute renal failure: clinical features and therapeutic approach.
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Acute spontaneous tumor lysis presenting with hyperuricemic acute renal failure: clinical features and therapeutic approach.

机译:急性自发性肿瘤溶解伴高尿酸血症性急性肾功能衰竭:临床特征和治疗方法。

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BACKGROUND: Acute spontaneous tumor lysis syndrome (STLS) presenting with hyperuricemic acute renal failure (ARF) is a rare disease which can be overlooked in patients with neoplasic disorders, requiring prompt recognition and aggressive management. This study examined the incidence, clinical characteristics and prognosis of this condition. METHODS: A retrospective study was performed, reviewing the records of all patients who developed ARF at Chang Gung Memorial Hospital between 1st July 1999 and 30th October 2002. Acute STLS was diagnosed based on pretreatment hyperuricemic ARF, ratio of urinary uric acid to creatinine (Cr) >1.0, and significantly elevated lactate dehydrogenase (LDH) (>500 units/L), together with a pathologically proven malignancy. Clinical course, metabolic parameters, response to therapeutics and outcome were assessed in all patients. RESULTS: STLS-induced acute uric acid nephropathy was identified in 10 out of 926 ARF patients (1.08%) studied. Most presentations were non-specific or related to malignancy symptoms. All patients had advanced tumors with large tumor burden, and abdominal organ involvement in 80% of patients. The 10 hyperuricemic patients became oliguric despite conservative therapy, and remained hyperuricemic (mean +/- SD: 20.7 +/- 5.0 mg/dL) until dialysis initiation. Seven patients (70%) developed diuresis, with an associated resolution of hyperuricemia, azotemia and metabolic derangements following dialysis initiation. The patients who developed diuresis had mean serum uric acid levels 9.3 +/- 3.1 mg/dL and median levels 9.8 mg/dL. Three patients (30%) survived, with two patients suffering residual renal function impairment. CONCLUSIONS: Acute STLS presenting with hyperuricemic ARF is a rare cause of acute uric acid nephropathy in patients with bulky or occult neoplastic disorders. The tumors that developed STLS had advanced stage or large tumor burden. Frequent abdominal organ involvement and non-specific initial presentations can obscure the nature of the disease and delay diagnosis. Unlike hyperuricemia and oliguria, which are constant findings, azotemia or impaired renal function is not always manifest on initial presentation. Poor outcomes in patients with STLS developing acute uric acid nephropathy make early recognition, aggressive management and prompt dialysis mandatory.
机译:背景:伴有高尿酸血症性急性肾衰竭(ARF)的急性自发性肿瘤溶解综合征(STLS)是一种罕见疾病,在赘生性疾病患者中可以忽略,需要迅速识别和积极治疗。这项研究检查了这种情况的发生率,临床特征和预后。方法:回顾性研究,回顾了1999年7月1日至2002年10月30日期间在长庚纪念医院发生ARF的所有患者的记录。根据治疗前的高尿酸ARF,尿酸与肌酐的比值(Cr )> 1.0,且乳酸脱氢酶(LDH)显着升高(> 500单位/ L),并经病理证实为恶性肿瘤。在所有患者中评估了临床过程,代谢参数,对治疗的反应和结果。结果:在研究的926名ARF患者中,有10名(1.08%)发现了STLS诱导的急性尿酸肾病。大多数表现是非特异性的或与恶性症状有关。所有患者均患有晚期肿瘤,肿瘤负担大,80%的患者累及腹部器官。尽管采用了保守疗法,这10名高尿酸血症患者仍处于低尿状态,并保持高尿酸血症(平均+/- SD:20.7 +/- 5.0 mg / dL)直至开始透析。七名患者(70%)发展为利尿,伴随透析开始后高尿酸血症,氮质血症和代谢紊乱的相关消退。发生利尿的患者的平均血清尿酸水平为9.3 +/- 3.1 mg / dL,中位水平为9.8 mg / dL。 3例患者(30%)存活,其中2例患者残余肾功能受损。结论:急性STLS伴有高尿酸血症ARF是大块或隐匿性肿瘤性疾病患者急性尿酸肾病的罕见原因。发生STLS的肿瘤具有晚期或较大的肿瘤负担。频繁的腹部器官受累和非特异性最初表现会掩盖疾病的本质并延误诊断。不像高尿酸血症和少尿症(这是不断发现的),氮缺乏症或肾功能受损并不总是在初次就诊时出现。 STLS发生急性尿酸肾病的患者预后差,因此必须尽早识别,积极管理并迅速进行透析。

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