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获得性呼吸纤毛超微结构改变与临床疾病。综述。

Acquired ultrastructural alterations of respiratory cilia and clinical disease. A review.

作者信息

Ballenger J J

机构信息

Division of Otolaryngology/Head and Neck Surgery, Evanston Hospital, Illinois.

出版信息

Ann Otol Rhinol Laryngol. 1988 May-Jun;97(3 Pt 1):253-8. doi: 10.1177/000348948809700308.

DOI:10.1177/000348948809700308
PMID:3288074
Abstract

Efficient cleansing of the upper and lower respiratory surfaces by the mucociliary apparatus is essential to health. Failure of the cleansing allows contaminants prolonged residence on the mucosal respiratory surfaces and thus penetration into the mucosa and possibly inauguration of disease. For some years, genetic ultrastructural ciliary alterations have been recognized, with symptoms dating from early life. It is only in recent years, however, that evidence has shown that ultrastructural ciliary alterations can be acquired later in life and that these alterations in turn lead to a deterioration of efficient ciliary cleansing. A discussion of the ultrastructure of the normal mammalian cilium will be given, as well as a listing of the genetic ciliary disease and their characteristic morphologic alterations. A more complete review will be made in regard to acquired ciliary defects, their cause, the ultrastructural changes, and the relation to clinical disease.

摘要

黏液纤毛装置对上、下呼吸道表面进行有效清洁对健康至关重要。清洁功能失效会使污染物长时间停留在呼吸道黏膜表面,进而穿透黏膜并可能引发疾病。多年来,人们已经认识到遗传导致的超微结构纤毛改变,症状始于早年。然而,直到最近才有证据表明,超微结构纤毛改变可能在生命后期出现,而这些改变反过来又会导致有效纤毛清洁功能的恶化。本文将讨论正常哺乳动物纤毛的超微结构,以及遗传性纤毛疾病及其特征性形态学改变。还将更全面地综述获得性纤毛缺陷、其病因、超微结构变化以及与临床疾病的关系。

相似文献

1
Acquired ultrastructural alterations of respiratory cilia and clinical disease. A review.获得性呼吸纤毛超微结构改变与临床疾病。综述。
Ann Otol Rhinol Laryngol. 1988 May-Jun;97(3 Pt 1):253-8. doi: 10.1177/000348948809700308.
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Secondary ciliary dyskinesia in upper respiratory tract.上呼吸道的继发性纤毛运动障碍
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[Survey of diseases in the mucociliary system. Cilia are the first defense organs of the respiratory tract].[黏液纤毛系统疾病调查。纤毛是呼吸道的第一道防御器官]
Lakartidningen. 1995 Aug 30;92(35):3097-102, 3105.
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Aplasia of respiratory tract cilia.
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[What is established in the immotile cilia syndrome?].[不动纤毛综合征中确立了什么?]
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Ultrastructural ciliary defects in children with recurrent infections of the lower respiratory tract.患有下呼吸道反复感染儿童的超微结构纤毛缺陷
Pediatr Pulmonol. 1991;10(1):11-7. doi: 10.1002/ppul.1950100104.
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Ciliary dyskinesia and ultrastructural abnormalities in respiratory disease.呼吸系统疾病中的纤毛运动障碍和超微结构异常。
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Ciliary abnormalities in children (hockey-stick cilia). Study by scanning electron microscope. Report on three paediatric cases.儿童睫状体异常(曲棍球棒状睫状体)。扫描电子显微镜研究。三例儿科病例报告。
Acta Otorhinolaryngol Belg. 1984;38(3):337-44.
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[How useful is the ultrastructural study of the cilia of the respiratory tract in the diagnosis of an immotile cilia syndrome?].[呼吸道纤毛超微结构研究在诊断纤毛不动综合征中具有多大作用?]
Schweiz Med Wochenschr. 1984 May 5;114(18):610-9.

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2
Retinitis pigmentosa and the question of photoreceptor connecting cilium defects.视网膜色素变性与光感受器连接纤毛缺陷问题
Graefes Arch Clin Exp Ophthalmol. 1995 May;233(5):275-83. doi: 10.1007/BF00177649.
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Ultrastructure and mucociliary transport of bronchial respiratory epithelium in intubated patients.
Intensive Care Med. 1995 Jun;21(6):482-9. doi: 10.1007/BF01706201.
4
Regeneration of respiratory epithelia in the rat after free grafting.大鼠游离移植后呼吸道上皮的再生
Eur Arch Otorhinolaryngol. 1992;249(7):359-63. doi: 10.1007/BF00192254.