Lotfi M, Brandwein J M
Department of Medicine, St. Michael's Hospital, University of Toronto, Ontario, Canada.
Leuk Lymphoma. 1998 May;29(5-6):625-8. doi: 10.3109/10428199809050923.
Acute tumor lysis syndrome (ATLS), a condition which results from a rapid destruction of tumor cells with massive release of cellular breakdown products, has been well described following the treatment of various malignancies. However, only a handful of cases of spontaneous ATLS have been reported in the literature. We describe the first reported case of spontaneous ATLS in acute myeloid leukemia (AML). A previously healthy 63 year old woman presented with a two month history of fatigue and a one week history of easy bruising. On admission she had oliguric acute renal failure, with marked elevation in serum uric acid and phosphate. A bone marrow biopsy showed AML M7 with fibrosis. The renal failure resolved with supportive care and institution of allopurinol therapy. Following this, AML induction chemotherapy resulted in complete remission. Her biochemical and clinical course were very similar to the classical ATLS seen in patients after chemotherapy. Therefore, this case represents a rare instance of acute renal failure from spontaneous ATLS, and in our opinion the first reported occurrence of spontaneous ATLS associated with AML.
急性肿瘤溶解综合征(ATLS)是一种因肿瘤细胞迅速破坏并大量释放细胞分解产物而导致的病症,在各种恶性肿瘤的治疗后已有详尽描述。然而,文献中仅报道了少数几例自发性ATLS病例。我们描述了首例急性髓系白血病(AML)伴自发性ATLS的报道病例。一名既往健康的63岁女性,有两个月的疲劳史和一周的易瘀伤史。入院时她出现少尿性急性肾衰竭,血清尿酸和磷酸盐显著升高。骨髓活检显示为伴有纤维化的AML M7。通过支持治疗和应用别嘌醇治疗,肾衰竭得以缓解。此后,AML诱导化疗导致完全缓解。她的生化和临床过程与化疗后患者中所见的经典ATLS非常相似。因此,该病例代表了自发性ATLS导致急性肾衰竭的罕见实例,并且在我们看来是首例报道的与AML相关的自发性ATLS病例。