Histopathologic alterations of nasal epithelium in chronic respiratory patients
Abstract
The epithelial lining of the respiratory airways and mucociliary transport play an important role in the primary defense mechanism of the respiratory system. Conditions that disrupt epithelium integrity or impair mucociliary clearance lead or favor chronic respiratory disease. In the present study we analyzed the nasal epithelium of 33 chronic respiratory patients using high-resolution histology and scanning electron microscopy. All the biopsies analyzed showed some degree of epithelial abnormality, and in no case the normal ciliated columnar pseudostratified epithelium was observed. In 17 patients, ciliated epithelia showing different types of alterations were recognized, whereas in the remaining 16 cases, ciliated cells were completely substituted by non-ciliated cell types, such as basal, goblet and squamous cells. In 27% of patients, epithelial alterations were seen in patients diagnosed of primary ciliary diskinesia, whereas in 52% of the cases, they appeared associated with secondary ciliary alterations or lack of cilia. In the remaining 21% of cases, disrupted epithelia were observed in patients with normal ciliary ultrastructure. These observations indicate that epithelial alterations may be the consequence of primary ciliary disorders or result from the sustained injury provoked by several chronic respiratory diseases, such as pneumonia, bronchitis, rhinitis, sinusitis and asthma. Considering that chronic inflammation and infection delay regeneration of the normal epithelium, early diagnosis is recommended to avoid installation of irreversible non-ciliated epithelial morphologies.
References
2) Mygind N, Pedersen N, Nielsen MH. Morphology of the upper airway epithelium. In: Proctor DF, Andersen I., eds. The nose: upper airway physiology and atmospheric environment. New York: Elsevier; 1982: 71-97.
3) Boysen M. The surface structure of the human nasal mucosa. I. Ciliated and metaplastic epithelium in normal individuals. A correlated study by scanning/transmission electron and light microscopy. Virchows Arch B Cell Pathol Incl Mol Pathol 1982; 40(3): 279-94.
4) Schrodter S, Biermann E, Halata Z. Histological evaluation of age-related changes in human respiratory mucosa of the middle turbinate. Anat Embryol (Berl) 2003; 207(1): 19-27.
5) Cowan MJ, Gladwin MT, Shelhamer JH. Disorders of ciliary motility. Am J Med Sci 2001; 321(1): 3-110.
6) Afzelius BA. Genetics and pulmonary medicine. Immotile cilia syndrome: past, present and prospects future. Thorax 1998; 53(10): 894-7.
7) Jorgensen F, Petruson B, Hansson HA. Extensive variations in nasal mucosa in infants with and without recurrent acute otitis media. A scanning electron-microscopic study. Arch Otolaryngol Head Neck Surg 1989; 115(5): 571-80.
8) Gaillard D, Jouet JB, Egreteau L, Plotkowski L, Zahm JM, Benali R, et al. Airway epithelial damage and inflammation in children with recurrent bronchitis. Am J Respir Crit Care Med 1994; 150(3): 810-7.
9) Chapelin C, Coste A, Gilain L, Poron F, Verra F, Escudier E. Modified epithelial cell distribution in chronic airways inflammation. Eur Respir J 1996; 9(12):2474-8.
10) Muller KM, Schmitz I. Chronic bronchitis – alterations of the bronchial mucosa. Wiad Lek 1997; 50(10-12): 252-66.
11) Al-Rawi MM, Edelstein DR, Erlandson RA. Changes in nasal epithelium in patients with severe chronic sinusitis: a clinicopathologic and electron microscopic study. Laryngoscope 1998; 108(12): 1816-23.
12) Boysen M, Reith A. Surface structures in normal, metaplastic and dysplastic nasal mucosa of nickel workers. A SEM and post SEM histopathological study. Scan Electron Microsc 1980; 3: 35-41.
13) Gulisano M, Pacini P, Merceddu S, Orlandini GE. Scanning electron microscopic evaluation of the alterations induced by polluted air in the rabbit bronchial epithelium. Anat Anz 1995; 177(2): 125-31.
14) Wright JL, Churg A. Smoking cessation decreases the number of metaplastic secretory cells in the small airways of the Guinea pig. Inhal Toxicol 2002; 14(11): 1153-9.
15) Brauer MM, Viettro L. Aportes de la microscopía electrónica de transmisión al diagnóstico de la disquinesia ciliar. Rev Méd Urug 2003; 19(2): 140-8.
16) Gulisano M, Pacini S, Ruggiero M, Pacini A, Delrio AN, Pacini P. In vitro effects of some differentiation inductors in metaplastic epithelium of human nasal cavity. Cell Tissue Res 1996; 285(1): 119-25.
17) Toskala E, Nuutinen J, Rautiainen M. Scanning electron microscopy findings of human respiratory cilia in chronic sinusitis and in recurrent respiratory infections. J Laryngol Otol 1995; 109(6):5 09-14.
18) Joki S, Toskala E, Saano V, Nuutinen J. Correlation between ciliary beat frequency and the structure of ciliated epithelia in pathological human nasal mucosa. Laryngoscope 1998; 108(3): 426-30.
19) Biedlingmaier JF, Trifillis A Comparison of CT scan and electron microscopic findings on endoscopically harvested middle turbinates. Otolaryngol Head Neck Surg 1998; 118(2): 165-73.
20) Trevisani L, Sartori S, Bovolenta MR, Mazzoni M, Pazzi P, Putinati S, et al. Structural characterization of the bronchial epithelium of subjects with chronic bronchitis and in asymptomatic smokers. Respiration 1992; 59(2): 136-44.
21) Harkema JR, Wagner JG. Non-allergic models of mucous cell metaplasia and mucus hypersecretion in rat nasal and pulmonary airways. Novartis Found Symp 2002; 248:181-97.
22) Lin CY, Cheng PH, Fang SY. Mucosal changes in rhinitis medicamentosa. Ann Otol Rhinol Laryngol 2004; 113(2): 147-51.
23) Pacini P, Gulisano M, Dallai S, Polli G, Gheri G. The human nasal mucous membrane during chronic inflammation, before and after muco-active therapy: a study using scanning electron microscopy. Ital J Anat Embryol 1993; 98(4): 231-41.
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