Kang Suzie Hyeona, Piltcher Otávio Bejzman, Dalcin Paulo de Tarso Roth
Programa de Pós-Graduação em Ciências Pneumológicas, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Int Forum Allergy Rhinol. 2014 Mar;4(3):223-31. doi: 10.1002/alr.21266. Epub 2014 Jan 10.
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.
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.
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.
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.
几乎所有囊性纤维化(CF)患者在计算机断层扫描(CT)中均显示上呼吸道受累。鼻窦病理学已成为一个具有挑战性的问题,因为几乎没有研究可指导适当的管理。本研究的目的是提供有关CF患者鼻窦CT表现的信息,主要是成年患者。
我们使用以下数据库对关于CF患者鼻窦CT表现的描述性研究进行了文献综述:MEDLINE、EMBASE、科学网、拉丁美洲和加勒比地区卫生科学数据库、科学电子图书馆在线和考克兰图书馆。
本综述纳入了18篇文章。大多数研究在方法学方面存在很大差异。CT扫描中报告的最常见表现为鼻窦混浊、额窦和蝶窦发育不全或发育不良、鼻窦发育不足以及鼻外侧壁内侧膨出。
关于CF成年人群鼻窦CT改变的研究很少。许多研究报告了CF上呼吸道的特定病理特征,这有助于诊断疑难病例。