Choanal atresia: Histochemical, immunohistochemical and ultrastructure study of the nasal mucosa
Abstract Objectives To study the nasal mucosal changes in cases with choanal atresia at the light and electron microscope and to compare the results with the normal side in unilateral cases. Study design Cross sectional study. Setting Tertiary University hospital, departments of Otolaryngology and p...
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Veröffentlicht in: | International journal of pediatric otorhinolaryngology 2015-02, Vol.79 (2), p.170-174 |
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Zusammenfassung: | Abstract Objectives To study the nasal mucosal changes in cases with choanal atresia at the light and electron microscope and to compare the results with the normal side in unilateral cases. Study design Cross sectional study. Setting Tertiary University hospital, departments of Otolaryngology and pathology. Methods Sixteen patients diagnosed to have choanal atresia (seven bilateral and nine unilateral); ranging in age from 3 days to 9 years; were included in this study. During surgical repair, a biopsy of the inferior turbinate mucosa was taken. Biopsy from patent side in unilateral choanal atresia was also taken (as a control). Then biopsies were subjected to histopathological, histochemical, immunohistochemical and ultrastructure studies. Results The nasal mucosa in choanal atresia side (weather unilateral or bilateral) showed distorted cilia, marked increase of mucous submucosal glands associated with marked reduction of goblet cell density and lymphocytic cellular infiltration. The patent side (control) showed normal respiratory epithelium with obviously noted intra-epithelial goblet cells. Submucosal glands were less in number and activity than in the atretic side. Conclusions Choanal atresia showed a condition of the nasal mucous membrane with characteristic excessive nasal tenacious secretion; mostly actively secreted besides some effect of lack of drainage due to interrupted cilia. Further studies are required to evaluate the impact of atresia repair on detected features. |
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ISSN: | 0165-5876 1872-8464 |
DOI: | 10.1016/j.ijporl.2014.11.035 |