Complete Ciliary Aplasia; a Rare Form of Primary Ciliary Dyskinesia
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Case report
VOLUME: 11 ISSUE: 3
P: 121 - 123
September 2010

Complete Ciliary Aplasia; a Rare Form of Primary Ciliary Dyskinesia

Turk Thorac J 2010;11(3):121-123
1. Atatürk Chest Disease and Chest Surgery Hospital, Department of Pulmonary Disease, Ankara, Turkey
2. Ankara University, Faculty of Medicine, Department of Histology and Embryology, Ankara, Turkey
No information available.
No information available
Accepted Date: 18.07.2019
Online Date: 18.07.2019
Publish Date: 18.07.2019
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Abstract

Abstract

This report describes the ultrastructural alterations observed in the bronchial mucosa of a 29-year old male patient suffering from chronic upper and lower respiratory tract infections since his childhood and operated due to bronchiectasis and sinusitis. Electron microscopic evaluation of the bronchial biopsy specimens revealed ciliated cells appeared to be replaced by columnar cells lacking cilia and basal bodies, and bearing on their surface ciliumlike projections without any internal axonemal structure. These ultrastructural features are consistent with complete ciliary aplasia which is a rare form of primary ciliary dyskinesia. (Tur Toraks Der 2010; 11: 121-3)

Keywords:
Ciliary aplasia, dyskinesia, bronchiectasis