Caruso Giuseppi, Gelardi Matteo, Passali Giulio C, de Santi Maria M
Ear, Nose, and Throat Department, University of Siena, Siena, Italy.
Am J Rhinol. 2007 Nov-Dec;21(6):702-5. doi: 10.2500/ajr.2007.21.3107.
Primary ciliary dyskinesia (PCD) is a congenital, clinically and ultrastructurally heterogeneous disease caused by abnormal structure and/or function of cilia. Kartagener's syndrome is one subgroup of PCD. Acquired ciliary dyskinesia is frequent, generally being associated with or following respiratory tract infections.
From January 2003 to April 2006, nasal mucociliary transport time was measured in 64 patients and specimens obtained by nasal scraping were examined by transmission electron microscope (TEM).
The 64 nasal scrapings led to the diagnosis of 11 (17.2%) cases of PCD and 51 (79.7%) cases of secondary ciliary disorder. In two cases (3.1%) no clear diagnosis was possible.
Nasal scraping is an easy, cheap, and efficient tool for detecting ciliary abnormalities by TEM and for distinguishing acquired and congenital modifications.
原发性纤毛运动障碍(PCD)是一种由纤毛结构和/或功能异常引起的先天性疾病,在临床和超微结构上具有异质性。卡塔格内综合征是PCD的一个亚组。获得性纤毛运动障碍很常见,通常与呼吸道感染有关或继发于呼吸道感染。
2003年1月至2006年4月,对64例患者测量鼻黏膜纤毛转运时间,并通过透射电子显微镜(TEM)检查鼻刮片获取的标本。
64份鼻刮片诊断出11例(17.2%)PCD和51例(79.7%)继发性纤毛疾病。2例(3.1%)无法明确诊断。
鼻刮片是一种简便、廉价且高效的工具,可通过TEM检测纤毛异常,并区分获得性和先天性改变。