Takahashi N, Maruta A, Hashimoto C, Kato K, Tanabe J, Kodama F, Omine M
Division of Hematology, Department of Internal Medicine, Showa University Fujigaoka Hospital.
Rinsho Ketsueki. 2000 Nov;41(11):1158-63.
A 45-year-old man was diagnosed as having Ph1+ acute lymphocytic leukemia (ALL) in February 1997. Complete remission was achieved by chemotherapy. Allogeneic BMT from his HLA-identical sister was performed on June 11, 1997. Engraftment was relatively quick, but acute GVHD (grade I) developed. The patient was discharged on day 113. Seven months after BMT, in January 1998, exertional dyspnea developed gradually. Chest X-ray examination showed diffuse interstitial pneumonia, for which corticosteroid was started immediately. The symptoms and signs gradually improved. However, on the 20th hospital day (February 23), bilateral subcutaneous emphysema developed in the neck and supraclavicular region. Chest X-ray and CT examinations showed pneumomediastinum without pneumothorax. The pneumomediastinum and subcutaneous emphysema gradually subsided after 3 weeks of bed rest. Subcutaneous emphysema and pneumomediastinum are relatively rare complications of allogeneic BMT.
一名45岁男性于1997年2月被诊断为Ph1+急性淋巴细胞白血病(ALL)。通过化疗实现了完全缓解。1997年6月11日接受了来自其 HLA 匹配姐姐的异基因骨髓移植。植入相对较快,但发生了急性移植物抗宿主病(I级)。患者于第113天出院。骨髓移植七个月后,即1998年1月,逐渐出现劳力性呼吸困难。胸部X线检查显示弥漫性间质性肺炎,立即开始使用皮质类固醇治疗。症状和体征逐渐改善。然而,在住院第20天(2月23日),颈部和锁骨上区域出现双侧皮下气肿。胸部X线和CT检查显示纵隔气肿,无气胸。卧床休息3周后,纵隔气肿和皮下气肿逐渐消退。皮下气肿和纵隔气肿是异基因骨髓移植相对罕见的并发症。