The early events in the healing of laser-produced tympanic membrane perforation
Abstract Conclusion: An immense keratinocyte activity with high cell turnover produced keratin that was delivered to span the perforation. The perforation size did not define the time to closure. Objectives: Most tympanic membrane perforations heal spontaneously, whereas a fraction remains patent. A...
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Published in | Acta oto-laryngologica Vol. 131; no. 5; pp. 480 - 487 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Stockholm
Informa Healthcare
01.05.2011
Taylor & Francis Informa |
Subjects | |
Online Access | Get full text |
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Summary: | Abstract
Conclusion: An immense keratinocyte activity with high cell turnover produced keratin that was delivered to span the perforation. The perforation size did not define the time to closure. Objectives: Most tympanic membrane perforations heal spontaneously, whereas a fraction remains patent. A simple, nonsurgical cure for chronic perforations is required. Better understanding of the healing processes might enable the development of a simple medical cure. Therefore the structural events of the healing process were investigated, as well as its dynamics, by comparing perforation size with time to closure. Methods: Twenty-four Sprague-Dawley rats were myringotomized with a KTP laser. Different perforation sizes were produced. The 'early closing picture' was assessed with otomicroscopy and light and transmission electron microscopy at between 1 h and 2 weeks after myringotomy and perforation size was monitored until closure. Results: In all, 40% of the perforations were closed after 8 days and 89% at 12 days. The closing time did not directly correlate with perforation size. A wave of keratinocytes migrates towards the perforation site and disintegrates to form a keratin mass that eventually spans the perforation. A less intense activity is present near the annulus. The origin of the epithelial migration is probably regenerative centers. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0001-6489 1651-2251 1651-2251 |
DOI: | 10.3109/00016489.2010.533696 |