Wester J P, Breumelhof R, Geers A B, Meuwissen O J
St.-Antonius Ziekenhuis, afd. Interne Geneeskunde, Nieuwegein.
Ned Tijdschr Geneeskd. 1997 Aug 16;141(33):1621-3.
A 20-year-old man was hospitalised because he nearly suffocated when lying on his back. After bronchoscopy which revealed severe external compression of the airways, suddenly respiratory insufficiency developed. Because a malignant lymphoma was suspected chemotherapy was started, using monotherapy with prednisolone as the risk of acute tumour lysis syndrome (ATLS) is high with polychemotherapy of bulky tumours. Nevertheless ATLS developed, for which haemodialysis had to be applied. The tumour, a T-cell lymphoblastic non-Hodgkin lymphoma with high grade malignancy, was treated successfully with cyclophosphamide, doxorubicin, vincristine en prednisone. ATLS is characterized by hyperkalaemia, hyperuricaemia, hyperphosphataemia, hypocalcaemia, lactate acidosis and acute renal failure. It can occur in the course of aggressive cytoreductive therapy in rapidly growing lymphoproliferative malignancies with large tumour size, due to massive tumour cel lysis. Corticosteroid monotherapy is a very rare cause of ATLS.
一名20岁男子因仰卧时几乎窒息而住院。支气管镜检查显示气道严重受压,随后突然出现呼吸功能不全。由于怀疑患有恶性淋巴瘤,开始进行化疗,鉴于大体积肿瘤采用多药化疗发生急性肿瘤溶解综合征(ATLS)的风险很高,故采用泼尼松龙单药治疗。然而,仍发生了ATLS,为此不得不进行血液透析。该肿瘤为高恶性T细胞淋巴母细胞性非霍奇金淋巴瘤,经环磷酰胺、阿霉素、长春新碱和泼尼松成功治疗。ATLS的特征为高钾血症、高尿酸血症、高磷血症、低钙血症、乳酸酸中毒和急性肾衰竭。它可发生于肿瘤体积大、生长迅速的淋巴增殖性恶性肿瘤进行积极细胞减灭治疗过程中,原因是大量肿瘤细胞溶解。皮质类固醇单药治疗是ATLS非常罕见的病因。