Matsuda S, Saitoh Y, Kanbayashi H, Tanaka T, Sakuma H, Maruyama Y, Ohno R
Center for Hematopoietic Disorders, Ohta Nishinouchi Hospital.
Rinsho Ketsueki. 1993 Sep;34(9):1033-8.
A 46-year-old woman with acute promyelocytic leukemia (APL) was treated with all-trans retinoic acid (ATRA) and chemotherapy according to the AML-92, M3 regimen of the Japan Adult Leukemia Study Group (JALSG). Between days 7 and 18 of therapy, she suffered chest discomfort, fever, cough, dyspnea and general fatigue. A chest roentogenogram showed bilateral interstitial infiltrates. Her leukocyte count began to increase rapidly to 6,400/microliters on day 14. Marked hypoxia (PO2 35.9 mmHg) suggested occurrence of retinoic acid (RA) syndrome. She underwent endotracheal intubation and mechanical ventilation with administration of methyl-prednisolone (m-PSL) pulse therapy. Her symptoms promptly abated. Therapy with ATRA was continued and her leukocyte count reached 44,800/microliters on day 19 of therapy. She achieved complete remission on day 48.
一名46岁的急性早幼粒细胞白血病(APL)女性患者,按照日本成人白血病研究组(JALSG)的AML-92、M3方案,接受了全反式维甲酸(ATRA)和化疗。在治疗的第7天至第18天期间,她出现了胸部不适、发热、咳嗽、呼吸困难和全身乏力。胸部X线片显示双侧间质性浸润。她的白细胞计数在第14天开始迅速增加至6400/微升。明显的低氧血症(PO2 35.9 mmHg)提示维甲酸(RA)综合征的发生。她接受了气管插管和机械通气,并给予甲泼尼龙(m-PSL)冲击治疗。她的症状迅速缓解。继续使用ATRA治疗,在治疗的第19天,她的白细胞计数达到44800/微升。她在第48天实现了完全缓解。