Suppr超能文献

64例原发性纤毛运动障碍成人鼻窦疾病的批判性评估

Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia.

作者信息

Bequignon Emilie, Dupuy Laurence, Zerah-Lancner Francoise, Bassinet Laurence, Honoré Isabelle, Legendre Marie, Devars du Mayne Marie, Escabasse Virginie, Crestani Bruno, Maître Bernard, Escudier Estelle, Coste André, Papon Jean-François

机构信息

AP-HP, Hôpital Henri-Mondor⁻A Chenevier et Hôpital intercommunal, Services d'ORL et de Pneumologie, Créteil 94010, France.

INSERM, U955, Créteil 94010, France.

出版信息

J Clin Med. 2019 May 7;8(5):619. doi: 10.3390/jcm8050619.

Abstract

To date, no study precisely described ear, nose and throat (ENT) disease in adults with primary ciliary dyskinesia (PCD) and its relationship with ciliary function/ultrastructure. A retrospective study of standardized ENT data (exam, audiogram, sinus Computed tomography (CT), and bacteriology) was conducted in 64 adults with confirmed PCD who were followed in two ENT reference centers. Rhinorrhoea and hearing loss were the main symptoms. Symptom scores were higher in older patients. Nasal endoscopy was abnormal in all patients except one, showing nasal polyps in one-third of the patients and stagnant nasal mucus secretions in 87.5% of the patients. Sinus CT opacities were mainly incomplete and showed one-third of the patients with sinus hypoplasia and/or agenesis. Middle meatus mainly grew , and . Otitis media with effusion (OME), which is constant in childhood, was diagnosed in less than one-quarter of the patients. In two-thirds of the patients, audiogram showed hearing loss that was sensorineural in half of the patients. ENT disease severity was not correlated with ciliary function and ultrastructure, but the presence of OME was significantly associated with a forced expiratory volume (FEV1) < 70%. Rhinosinusitis is the most common clinical feature of PCD in adults, while OME is less frequent. The presence of active OME in adults with PCD could be a severity marker of lung function and lead to closer monitoring.

摘要

迄今为止,尚无研究精确描述原发性纤毛运动障碍(PCD)成年患者的耳鼻喉(ENT)疾病及其与纤毛功能/超微结构的关系。对64例确诊为PCD的成年患者进行了一项关于标准化耳鼻喉数据(检查、听力图、鼻窦计算机断层扫描(CT)和细菌学)的回顾性研究,这些患者在两个耳鼻喉参考中心接受随访。鼻漏和听力损失是主要症状。老年患者的症状评分更高。除1例患者外,所有患者的鼻内镜检查均异常,三分之一的患者有鼻息肉,87.5%的患者有鼻黏液分泌停滞。鼻窦CT混浊主要为不完全性,三分之一的患者有鼻窦发育不全和/或发育异常。中鼻道主要生长 , 以及 。儿童期常见的分泌性中耳炎(OME)在不到四分之一的患者中被诊断出。三分之二的患者听力图显示有听力损失,其中一半患者为感音神经性听力损失。耳鼻喉疾病的严重程度与纤毛功能和超微结构无关,但OME的存在与用力呼气量(FEV1)<70%显著相关。鼻窦炎是成年PCD患者最常见的临床特征,而OME则较少见。成年PCD患者中活动性OME的存在可能是肺功能的严重程度标志物,需要密切监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a5e/6571605/cd605917e9fb/jcm-08-00619-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验