山东大学学报 (医学版) ›› 2022, Vol. 60 ›› Issue (12): 58-62.doi: 10.6040/j.issn.1671-7554.0.2022.0386
• • 上一篇
梁子婷1*,许长娟1*,曾荣1,张锦涛1,曾庆师2,董亮1,3
LIANG Ziting1*, XU Changjuan1*, ZENG Rong1, ZHANG Jintao1, ZENG Qingshi2, DONG Liang1,3
摘要: 目的 分析儿童异基因造血干细胞移植(allo-HSCT)术后并发闭塞性细支气管炎综合征(BOS)的临床特征。 方法 收集2014年8月至2021年3月于山东省千佛山医院住院行allo-HSCT后确诊BOS的9例患儿的病历资料,回顾性分析9例患儿的临床症状、胸部高分辨CT、肺功能、诊断以及治疗。 结果 9例患儿allo-HSCT术后出现BOS的时间为(9.3±4.4)个月,主要临床表现为干咳、气喘。BOS在胸部高分辨CT中的主要表现为支气管壁增厚、支气管扩张和马赛克征等。肺功能改变以阻塞性通气功能障碍同时伴有弥散功能下降为主。allo-HSCT后BOS的治疗主要以免疫抑制剂和糖皮质激素为主,9 例患儿治疗后均好转。 结论 BOS是儿童行allo-HSCT治疗后发生在肺部的排异表现,其临床表现、肺功能以及胸部CT表现缺乏特异性。BOS会造成肺部不可逆性损害,移植后患儿需规律行肺功能检查以早诊断、早治疗。
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