Sinonasal alterations in computed tomography scans in cystic fibrosis: a literature review of observational studies

被引:14
作者
Kang, Suzie Hyeona [1 ]
Piltcher, Otavio Bejzman [2 ]
Roth Dalcin, Paulo de Tarso [3 ]
机构
[1] Univ Fed Rio Grande do Sul, Fac Med, Programa Pograd Ciencias Pneumol, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Fac Med, Dept Ophthalmol & Otolaryngol, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Fac Med, Dept Internal Med, Porto Alegre, RS, Brazil
关键词
rhinosinusitis; computed tomography; paranasal sinus disease; cystic fibrosis; upper airway; PARANASAL SINUS DEVELOPMENT; PATHOLOGICAL-CHANGES; CT CHARACTERIZATION; DISEASE; SURGERY; NASAL; PANCREAS; GENOTYPE;
D O I
10.1002/alr.21266
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background Almost all cystic fibrosis (CF) patients reveal upper airway involvement in computed tomography (CT) scans. Sinonasal pathology has become a challenging issue because there are few studies to guide appropriate management. The objective of this study was to provide information about paranasal sinus CT manifestations in CF patients, mainly in adulthood. Methods We performed a literature review of descriptive studies about CT sinonasal findings in CF patients using the following databases: MEDLINE, EMBASE, Web of Science, LILACS, Scielo, and Cochrane. Results Eighteen articles were included in this review. There was a high variability in methodological aspects for most of the studies. The most prevalent findings reported were opacification of sinuses, presence of frontal and sphenoidal aplasia or hypoplasia, underdevelopment of paranasal sinuses, and medial bulging of the lateral nasal wall in CT scans. Conclusion There are few studies in the CF adult population regarding sinonasal CT alterations. Many studies report specific pathological features in CF upper airways that could help in the diagnosis of doubtful cases.
引用
收藏
页码:223 / 231
页数:9
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