Coating the acrylic resin dentures with Adper Single Bond Adhesive was effective in reducing C. albicans adhesion to dentures, while coating with 2-Octyl Cyanoacrylate adhesive completely inhibited such adhesion.
Thyroglossal duct cysts (TDCs) with ambiguous epithelial lining are the most common midline cervical anomaly encountered in children. To histopathologically study the epithelial lining of 32 thyroglossal duct cysts in relation to their locations. A total of 32 cases of thyroglossal duct cysts were collected for this study. The samples were classified into 3 groups as follows: (1) above the hyoid bone; (2) at the level of hyoid bone; (3) below the hyoid bone. All samples were H&E stained. Seventeen TDCs (53 %) were found above the hyoid bone, 6 (18.8 %) were found at the level of hyoid bone and 9 (28.1 %) were found below the hyoid bone. Of the 32 total cases, 6 (18.8 %) were lined with stratified squamous epithelium (SSE), 17 (53 %) were lined with pseudostratified ciliated epithelium (PSCE), 3 (9.4 %) were lined with stratified cuboidal epithelium (SCE), and 6 (18.8 %) exhibited both SSE and PSCE. Pseudostratified ciliated epithelium was dominant in the region superior to the hyoid bone, whereas SCE was detected only in TDCs at the level of hyoid bone. These differences were statistically significant (P = 0.0001). Different types of epithelial lining were detected in the study samples of TDCs. A statistically significant correlation was found between the type of epithelium detected and the location of the TDC at the time of diagnosis.
Background:
Oral cancer is usually diagnosed at advanced stages. The pattern of keratin expression in normal epithelia and the change in their expression in premalignant lesions and carcinomas have suggested the possibilities of improving diagnosis. The aim of this study is to determine the use of acidic cytokeratins (CKs) as biomarkers of histopathological progression in oral carcinogenesis.
Materials and Methods:
A total of 50 paraffin blocks of histological specimens diagnosed as hyperplastic epithelium, dysplastic epithelium, well-differentiated squamous cell carcinoma (SCC) and poorly-differentiated SCC (10 specimens each) were included in this study, in addition to 10 normal oral mucosal samples. All samples were stained immunohistochemically with CKs (10-ab1, 14, 16-ab1, 18-dc10 and 19-abs10) using Ventana Medical Systems (Arizona-USA). The expression of CKs antigen was evaluated as absent, mild, moderate and severe.
Results:
CK10-ab1 was found to be positive in the suprabasal layers of all specimens in normal and hyperplastic epithelium, while it was moderate in dysplastic epithelium and mild in well-differentiated SCC. CK10-ab1 was negative in all samples with poorly-differentiated SCC (
P
< 0.005). CK14 was positive in all specimens of all groups whereas CK16-ab1 was negative in all specimens of all groups. The stain of CKs 18-dc10 and 19-abs10 was restricted to the basal cells only in normal, hyperplastic and dysplastic epithelium, while it was mild in well-differentiated and poorly-differentiated SCC (
P
< 0.01).
Conclusion:
CK10-ab1 disappeared gradually with the progression of malignant changes of squamous cells whereas CKs 18-dc10 and 19-abs10 increased gradually at the same time. Such changes in the protein mapping of squamous cells need more investigation for a better understanding of oral SCC.
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