37 research outputs found

    Odontogenic keratocysts in Nevoid basal cell carcinoma syndrome: a case report

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    Nevoid basal cell carcinoma syndrome, a rare autosomal dominant disorder, comprises a number of abnormalities such as multiple nevoid basal cell carcinomas, skeletal abnormalities and multiple odontogenic keratocysts. Considering the rarity of this syndrome, we present a 12-year-old boy affected by this syndrome. He had multiple okcs, calcification of falx cerebri, bifid ribs, frontal bossing and hypertelorism. Characteristic cutaneous manifestation (nevoid basal cell carcinoma) was not present in this patient. The jaw cysts were treated with marsupialization then enucleation. The dental clinician may be the first to encounter and identify this syndrome, when the multiple cystlike radiolucencies are discovered on panoramic view

    Evaluation of the Relationship Between the Invasion Depth of Oral Squamous Cell Carcinoma and Clinicopathological Parameters

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    Background: This study aimed cohort study aimed to evaluate the relationship between the depth of invasion (DOI) and the lymphocytic host response (LHR) in oral squamous cell carcinoma (OSCC) biopsies with various clinicopathological characteristics of the disease.Materials and Method: Eighty-seven OSCC biopsy samples were obtained and key patient data such as clinical stage, grading, nodal involvement, overall survival (OS), and disease-free survival (DFS) were collected. DOI was measured from the basement membrane to the deepest invasion point, classifying samples into low risk (DOI 4 mm) categories. Additionally, LHR in the DOI was categorized as mild, moderate, or severe. The Chi-squared and Fisher’s exact test and Kaplan-Meier analysis were used for data analysis. The significance level was set at 0.05.Results: The findings revealed that 43.7% of patients fell into the low-risk DOI category, while 56.3% were in the high-risk group. LHR levels varied, with 36.8% mild, 18.4% moderate, and 44.8% severe. Most patients were in stage IV (31%) and grade I (60.9%). A significant relationship was found between the high-risk DOI group and several factors: disease stage (p < 0.001), grading (p = 0.021), five-year OS (p=0.001), five-year DFS (p < 0.001), and lymph node involvement (p < 0.001). Moreover, a significant relationship existed between LHR and the disease stage (p = 0.003) and lymph node involvement (p = 0.001).Conclusion: Incorporating DOI into routine histopathological reports could be beneficial in predicting OSCC prognosis, especially in early stages. This underscores the importance of histopathological evaluations in OSCC treatment planning, highlighting the value of DOI and LHR in understanding the disease's clinicopathological aspects

    Evaluation of the diagnostic value of a Modified Liquid-Based Cytology using OralCDx Brush in early detection of oral potentially malignant lesions and oral cancer

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    Objectives: To determine diagnostic value of modified Liquid Based Brush Biopsy technique. Study design: 26 oral premalignant and malignant lesions in 25 patients (12 females; 54.23±19.77 years and 13 males; 53.77±15.43 years) underwent Modified (Liquid Based) Brush Biopsy and scalpel biopsy simultaneously from the same area. Results: There were 16 positive and 10 negative brush biopsy results, with no inadequate readings. Histological findings were compatible with oral leukoplakia(n=5)with dysplasia, Oral lichen planus and lichenoid reaction(n=7) (with or without dysplasia)oral squamous cell carcinoma(n=11),verrucous carcinoma(n=1) and granular cell tumors( n=2). Sensitivity, specificity, positive predictive value, negative predictive value, positive diagnostic likelihood ratio(LR+) and negative diagnostic likelihood ratio(LR-) were 88.8%,100%,100% , 80%, infinity and 0.11 respectively(no false positive results). Conclusion: It is the first attempt to do LBC (liquid based cytology) with a specialized oral brush. Our results show that modified technique is a useful tool for screening of oral premalignant and malignant lesions

    Human Pulp Response to Direct Pulp Capping and Miniature Pulpotomy with MTA after Application of Topical Dexamethasone: A Randomized Clinical Trial

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    Introduction: The aim of this randomized clinical trial was to compare the histologic pulp tissue response to one-step direct pulp capping (DPC) and miniature pulpotomy (MP) with mineral trioxide aggregate (MTA) after application of dexamethasone in healthy human premolars. Methods and Materials: Forty intact premolars from 10 orthodontic patients, were randomly chosen for DPC (n=20) or MP (n=20). In 10 teeth from each group, after exposure of the buccal pulp horn, topical dexamethasone was applied over the pulp. In all teeth the exposed/miniaturely resected pulp tissue was covered with MTA and cavities were restored with glass ionomer. Teeth vitality was evaluated during the next 7, 21, 42, and 60 days. Signs and/or symptoms of irreversible pulpitis or pulp necrosis were considered as failure. According to the orthodontic schedule, after 60 days the teeth were extracted and submitted for histological examination. The Kruskal-Wallis and Fisher’s exact tests were used for statistical analysis of the data (P=0.05). Results: Although dexamethasone specimens showed less inflammation, calcified bridge, pulpal blood vasculature, collagen fibers and granulation tissue formation were not significantly different between the groups (P&gt;0.05). Conclusion: Topical dexamethasone did not hindered pulp healing but reduced the amount of underlying pulpal tissue inflammation after DPC and MP in healthy human premolars.Keywords: Dexamethasone; Direct Pulp Capping; Mineral Trioxide Aggregate; Miniature Pulpotomy; Vital Pulp Therap

    The expression of heat shock proteins 27 and 105 in squamous cell carcinoma of the tongue and relationship with clinicopathological index

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    Introduction: In oral cavity, the tongue is the most common site prone to development of squamous cell carcinoma (SCC). Considering malignant transformation as a cellular stress, the expression of heat shock proteins (HSPs) may be affected in this process. In this study we assessed the expression of HSP105 and HSP27 as two of the most interested stress proteins and investigated their relationship with grade and stage of the tongue SCC. Material and Methods: Fifty-six specimens including 31 early and 25 advanced tongue SCC were gathered. All specimens were graded histologically from I to III. Sixteen sections of normal oral mucosa were used as control group. The cellularity and intensity of HSP105 and HSP27 expression were studied immunohistochemically in both case and control groups. Results were expressed by histochemical score (HSCORE). Results: Significant differences were observed between expression of HSPs and stage of the disease. From early to advanced stage, the expression of HSP105 and HSP27 increased and decreased, respectively. There was no relationship between histological grade of lesion and HSCORE of HSP105 expression (P=0.5), although, HSP27 expression had reverse relationship with the SCC histological grade. Conclusion: HSP27 and HSP105 may be indicated for prognostic purposes in evaluation of tongue SCC. HSP 27 may be used for more accurate microscopic grading of tongue SCC. Increased expression of HSP105 in advanced stage may lead to using this protein for immunotherapy of tongue SCC. © Medicina Oral S. L

    Extragingival pyogenic granuloma: a case report

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    The pyogenic granuloma is thought to represent an exuberant tissue response to local irritation or trauma

    T-Cell Lymphoma of Palate with Nose and Maxillary Sinus Involvement: A Case Report

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    Oral cavity T-cell lymphoma occurs rarely. This case reportdescribes a patient with such a tumor. The case was a 75 yearsold man presented with a painless swelling on his hard palatemucosa. He had suffered from nose- bleeding and nasal obstruction.Pathology revealed the presence of a T-cell lymphomatumor in the palate. Though rare, the signs and symptomsof the case suggest that T-cell lymphoma should be consideredin the differential diagnosis of oral cavity lesions
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