Abstract:
Tracheobronchopathia osteochondroplastica (TO) is an orphan disease of the tracheobronchial tree without any known etiological attributes. There are several case reports published on this condition, yet the available information about the TO is discrete and of little clinical value. This scoping review is the first large-scale review on TO that collates individual patient data from the published case reports and descriptively analyses the clinicopathological features of this unique condition along with its management approaches and therapeutic outcomes. The objective was to synthesize comprehensive literature review on TO that can aid clinical practice and further research. An electronic search conducted in five large databases, including PubMed, EMBASE, CINAHL, CENTRAL, and Web of Science, for the published articles of TO yielded 1072 items. After screening, the individual patient data of 371 TO cases from 228 eligible articles were included and analysed in this scoping review.
UNASSIGNED: The online version contains supplementary material available at 10.1007/s12070-023-03998-6.
摘要:
气管支气管病(TO)是气管支气管树的孤儿疾病,没有任何已知的病因。在这种情况下有几份病例报告发表,然而关于TO的现有信息是离散的,几乎没有临床价值.本范围审查是对TO进行的首次大规模审查,该审查从已发表的病例报告中整理了个体患者数据,并描述性地分析了这种独特状况的临床病理特征及其管理方法和治疗结果。目的是综合有关TO的综合文献综述,以帮助临床实践和进一步研究。在五个大型数据库中进行的电子搜索,包括PubMed,EMBASE,CINAHL,中部,和WebofScience,对于TO的已发表文章,产生了1072个项目。筛选后,本范围审查纳入并分析了228篇符合条件的文献中的371例TO患者的个体数据.
■在线版本包含补充材料,可在10.1007/s12070-023-03998-6获得。