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不动纤毛综合征患者支气管上皮的变化。

Changes in the bronchial epithelia in patients with immotile cilia syndromes.

作者信息

Biczysko Wiesława, Marszałek Andrzej, Seget Monika, Breborowicz Anna, Goździk Joanna, Sierakowska-Urbańska Grazyna

机构信息

Department of Clinical Pathomorphology, University of Medical Sciences, Poznań, Poland.

出版信息

Folia Morphol (Warsz). 2003 Nov;62(4):393-5.

Abstract

Immotile cilia syndromes is a cause of recurrent infection of the airways and recurrent bronchopneumonias. Among the ciliary abnormalities are found changes in the structure of the microtubules, unco-ordinated ciliary movements caused by the absence of inner or outer or both dynein arms, and abnormalities of the kinetosomes and/or rete ridges. In patients with ciliary dyskinaesia bronchitis occurs early in life (during infancy) and usually has a recurrent tendency, so that bronchial biopsy is frequently undergone for diagnostic purposes. In this study we include 127 bronchial biopsies from patients (from 2 months to 49 years) unsuccessfully treated for recurrent respiratory tract infections. When performing regular diagnostic procedures on the light and electron microscopic level, we have looked for cilia abnormalities and also focused on changes within the mucosa and submucosa. The most common abnormality recorded was absence of the inner dynein arms, but in 40 cases neither of the dynein arms were present. Only a few patients had classical Kartagener's syndrome. Special attention is drawn to biopsies from elderly patients, in whom long-standing infections were followed by extensive damage to the bronchial epithelium, including even a total absence of ciliated cells. In some cases enhanced regenerative processes and some foci of squamous metaplasia were found. In two cases even foci of low-grade dysplasia were diagnosed.

摘要

不动纤毛综合征是气道反复感染和反复支气管肺炎的一个病因。在纤毛异常中可发现微管结构的改变、因缺少内或外动力蛋白臂或两者均缺如导致的不协调纤毛运动,以及动基体和/或网状嵴的异常。在纤毛运动障碍患者中,支气管炎在生命早期(婴儿期)就会出现,且通常有复发倾向,因此经常进行支气管活检以用于诊断。在本研究中,我们纳入了127例因反复呼吸道感染治疗无效的患者(年龄从2个月至49岁)的支气管活检标本。在进行光镜和电镜水平的常规诊断检查时,我们查找了纤毛异常情况,同时也关注了黏膜和黏膜下层的变化。记录到的最常见异常是缺少内动力蛋白臂,但有40例患者内、外动力蛋白臂均缺如。只有少数患者患有典型的卡塔格内综合征。特别值得注意的是老年患者的活检标本,在这些患者中,长期感染后支气管上皮出现广泛损伤,甚至包括纤毛细胞完全缺失。在一些病例中发现再生过程增强以及一些鳞状化生灶。在两例病例中甚至诊断出了低度发育异常灶。

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