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1.
Pan Afr Med J ; 33: 18, 2019.
Article in English | MEDLINE | ID: mdl-31312334

ABSTRACT

INTRODUCTION: odontogenic tumors originate from neoplastic transformation of the remnants of tooth forming apparatus. There are varying degrees of inductive interactions between odontogenic ectomesenchyme and epithelium during odontogenesis, leading to lesions that vary from benign to malignant. Malignant odontogenic tumours (MOTs) are very rare and are classified according to embryonic tissue of origin. Recently, there has been a few changes to the classification of MOTs according to the World Health Organization's (WHO) classification in 2017. This study aims to evaluate and reclassify MOTs, using a multi-centre approach in some major tertiary dental hospitals in Nigeria. METHODS: this study reviewed the clinicopathological data on 63 cases of MOT diagnosed over 25 years in five major tertiary dental hospitals in Nigeria. All MOT cases were reclassified according to the recent revision to the 2017 WHO classification of odontogenic tumours. RESULTS: from a total of 10,446 biopsies of oral and jaw lesions seen at the 5 study centres over the 25-year study period, 2199 (21.05%) cases were found to be odontogenic tumours (OTs), of which 63 were MOT. MOTs constituted 0.60% of the total biopsy cases and 2.86% of OTs. Odontogenic carcinomas presented with a mean age higher than odontogenic sarcomas. According to our 2017 WHO reclassification of MOTs, odontogenic carcinomas, ameloblastic carcinomas and primary intraosseous carcinomas were found to be the top three lesions, respectively. Carcinosarcomas were found to be extremely rare. CONCLUSION: using a multi-centre approach is a robust way to reduce diagnostic challenges associated with rare maxillofacial lesions such as MOTs.


Subject(s)
Ameloblastoma/epidemiology , Carcinosarcoma/epidemiology , Jaw Neoplasms/epidemiology , Odontogenic Tumors/epidemiology , Adolescent , Adult , Age Factors , Aged , Ameloblastoma/diagnosis , Ameloblastoma/pathology , Biopsy/methods , Carcinosarcoma/diagnosis , Carcinosarcoma/pathology , Child , Child, Preschool , Female , Humans , Jaw Neoplasms/diagnosis , Jaw Neoplasms/pathology , Male , Middle Aged , Nigeria/epidemiology , Odontogenic Tumors/diagnosis , Odontogenic Tumors/pathology , Retrospective Studies , Young Adult
2.
Afr Health Sci ; 19(1): 1677-1686, 2019 Mar.
Article in English | MEDLINE | ID: mdl-31148998

ABSTRACT

INTRODUCTION: Ameloblastoma is the most common odontogenic tumour in Nigeria. A definite geographic variation has been observed in the frequency of odontogenic tumors from different parts of the world. However, there is no study on the regional variations in Nigeria. Hence, this study was designed to document the ethnic and geographical distribution of jaw ameloblastoma in Nigeria. METHODS: Archival data on ameloblastoma from 10 health facilities were obtained. Global Moran's I detected geographic clustering in its distribution while Local Getis Ord indicated the location of ameloblastoma clusters. Chi-square tested associations between variables at 0.05 level of significance. RESULTS: A total of 1,246 ameloblastoma cases were recorded in Nigeria. Besides substantial state variations, a South-North gradient was noticed in its distribution. Significant positive spatial autocorrelation was observed in the three major groups while ameloblastoma hotspots were found in the SouthWestern and Northwestern Nigeria. The Igbos had a higher prevalence of ameloblastoma outside their home region than within. CONCLUSION: The study hypothesized that the geographical distribution of ameloblastoma in Nigeria is the result of all or one of the following: the country's tropical climate, migration patterns and health seeking behavior. Hopefully, these claims should lead to further enquiry on the underlying causes.


Subject(s)
Ameloblastoma/ethnology , Ethnicity/statistics & numerical data , Jaw Neoplasms/ethnology , Adolescent , Adult , Aged , Ameloblastoma/pathology , Cluster Analysis , Female , Hospitals, Teaching , Humans , Jaw Neoplasms/pathology , Male , Middle Aged , Nigeria/epidemiology , Prevalence , Spatial Analysis
3.
J Oral Pathol Med ; 48(5): 358-364, 2019 May.
Article in English | MEDLINE | ID: mdl-30839136

ABSTRACT

The present systematic review sought to evaluate the effects of Sodium Lauryl Sulfate (SLS)-free compared to SLS-containing dentifrices on (Recurrent) aphthous stomatitis (RAS) in patients with this condition. Cochrane, Medline (PubMed) and Embase databases, and some trial registries were searched through December 2017. There was no language, nor publication year restrictions. We included double-blinded randomized controlled trials that compared the effects of dentifrices with and without SLS on RAS in humans. Data extraction was compliant with PRISMA guidelines and the Cochrane Handbook for Systematic Reviews of Interventions. PROSPERO 2018:CRD42018086001. Four trials were included in this review (all crossover studies; n = 124 participants) and two contributed to the main meta-analysis based on the random-effect model. SLS-free dentifrice, when compared to SLS-containing statistically significantly, reduced the number of ulcers, duration of ulcer, number of episodes, and ulcer pain. Sensitivity analysis of the four studies as parallel-group trials shows a consistent direction of effect in favor of SLS-free dentifrice usage. In conclusion, the qualitative and quantitative synthesis of the eligible trials for this review showed that use of SLS-free consistently reduced all four parameters of ulcers measured. The available evidence suggests that patients with RAS may benefit from using SLS-free dentifrices for their daily oral care. However, future well-designed trials are still required to strengthen the current body of evidence.


Subject(s)
Dentifrices/adverse effects , Sodium Dodecyl Sulfate/adverse effects , Stomatitis, Aphthous/chemically induced , Stomatitis, Aphthous/drug therapy , Dentifrices/therapeutic use , Humans , Randomized Controlled Trials as Topic , Recurrence , Sodium Dodecyl Sulfate/therapeutic use
4.
Arch Oral Biol ; 98: 61-67, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30465934

ABSTRACT

OBJECTIVES: Ameloblastoma is an aggressive odontogenic jaw neoplasm. Its unlimited growth confers high potential for malignant transformation and recurrence. It is unclear why ameloblastoma is highly recurrent despite surgical resection with a wide margin of normal tissue. While canonical autophagy can be used to degrade and eliminate damaged cellular components, it is also a protective mechanism that provides energy and vital metabolites for cell survival. We used ameloblastoma-derived cells to test the hypothesis that autophagic processes play a role in survival and reactivation of ameloblastoma. METHODS: Primary epithelial (EP-AMCs) and mesenchymal (MS-AMCs) ameloblastoma-derived cells were established from tissue samples of solid multicystic ameloblastoma. Clonogenic capacity and basal autophagic capacity were assessed in ameloblastoma-derived cells relative to human odontoma-derived cells (HODCs) and maxilla-mesenchymal stem cells (MX-MSCs). Ability of ameloblastoma-derived cells to survive and form new ameloblastoma was assessed in mouse tumor xenografts. RESULTS: EP-AMCs were highly clonogenic (p < 0.0001) and demonstrated enhanced basal levels of autophagic proteins microtubule-associated protein 1-light chain 3 (LC3) (p < 0.01), p62 (Sequestosome 1, SQSTM1) (p < 0.01), and the LC3-adapter, melanoregulin (MREG) (p < 0.05) relative to controls. EP-AMCs xenografts regenerated solid ameloblastoma-like tumor with histological features of columnar ameloblast-like cells, loose stellate reticulum-like cells and regions of cystic degeneration characteristic of follicular variant of solid multicystic ameloblastoma. The xenografts also displayed stromal epithelial invaginations strongly reactive to LC3 and p62 suggestive of epithelial-mesenchymal transition and neoplastic odontogenic epithelium. CONCLUSIONS: EP-AMCs exhibit altered autophagic processes that can support survival and recurrence of post-surgical ameloblastoma cells.


Subject(s)
Ameloblastoma , Autophagy/physiology , Cell Survival , Odontogenic Tumors , Adaptor Proteins, Vesicular Transport , Ameloblastoma/pathology , Ameloblasts/metabolism , Ameloblasts/pathology , Animals , Carrier Proteins/metabolism , Disease Models, Animal , Epithelial-Mesenchymal Transition , Epithelium/metabolism , Female , Heterografts , Humans , Intracellular Signaling Peptides and Proteins , Mesenchymal Stem Cells , Mice , Microtubule-Associated Proteins/metabolism , Neoplasm Recurrence, Local , Sequestosome-1 Protein/metabolism , Xenograft Model Antitumor Assays
5.
Article in English | MEDLINE | ID: mdl-30126803

ABSTRACT

OBJECTIVES: Ameloblastoma is a benign, slow-growing, locally invasive epithelial tumor of odontogenic origin, with unlimited growth capacity and a strong tendency to recur. This multicentric study analyzed ameloblastoma diagnosed in Nigeria among different ethnic groups. STUDY DESIGN: This retrospective study included ameloblastoma cases diagnosed from 1964 to 2017 at 10 hospitals or medical centers in Nigeria. Age, sex, tribe, and location of the ameloblastoma in the jaw were analyzed. Associations between variables were tested by using χ2 and Fisher's exact test. RESULTS: A total of 1246 ameloblastoma cases were recorded (mean patient age 32.51 ± 14.54 years; range 4-86 years; male-to-female ratio 1.2:1). Approximately 60% of ameloblastoma cases occurred in young adults (age range 18-40 years). Ninety-eight lesions were located in the maxilla and 1103 in the mandible; the posterior mandible was the most common site (31.3% on the right and 26.5% on the left, respectively), followed by the anterior (26.0%) mandible. No significant differences were noted in the distribution of ameloblastoma within the tribes with respect to age (P = .92) and sex (P = .71). CONCLUSIONS: The mandible is a common site of ameloblastoma in patients in Nigeria, and in most cases, it occurs in young adults. Early presentation, diagnosis, and treatment are important to reduce postoperative disfigurement and morbidity.


Subject(s)
Ameloblastoma/ethnology , Jaw Neoplasms/ethnology , Adolescent , Adult , Aged , Aged, 80 and over , Ameloblastoma/pathology , Child , Child, Preschool , Female , Humans , Jaw Neoplasms/pathology , Male , Middle Aged , Nigeria/epidemiology , Retrospective Studies
6.
Pan Afr Med J ; 31: 25, 2018.
Article in English | MEDLINE | ID: mdl-30918552

ABSTRACT

INTRODUCTION: Dermatofibrosarcoma protuberance (DFSP) is in general a rare low grade malignant sarcoma and possesses a tendency for local recurrence. It has a site predilection for the trunk. Occurrence in the facial area is extremely rare. Ample knowledge of its clinical, histological and biologic characteristics is vital for accurate and prompt recognition. METHODS: Over 13 years, clinicohistologic information of cases was retrieved. Histological and immunohistochemical re-evaluation were performed to re-confirm diagnosis. Data collected and analyzed with SPSS Statistics version 20 were presented as frequency tables, charts and proportions as appropriate. RESULTS: Of 191 soft tissue sarcomas, a total of 28 cases were diagnosed as DFSP (14.7%). Facial types occurred in 3 cases (1.6%). Tumour had age and site predilections for the 4th decade and trunk respectively. There was an equal gender distribution among cases. Most common clinical presentation was in form of painless protruding nodular mass. General histologic presentation revealed cellular lesions composed of spindle to oval neoplastic cells arranged in a storiform pattern. Mitotic figures were rare. All cases showed positive expressions to CD34. CONCLUSION: Facial DFSP is rare among Nigerians. Its clinical appearance may mimic other common benign lesions of the head and neck region often resulting in misdiagnoses. A comprehensive knowledge of its clinical and histologic presentations and biologic behavior, combined with its identification with the aid of advanced histologic and radiographic techniques results in prompt confirmatory diagnosis. Appropriate treatment should include adequate surgical excision techniques combined with adjuvant radiotherapy or chemotherapy.


Subject(s)
Dermatofibrosarcoma/epidemiology , Facial Neoplasms/epidemiology , Skin Neoplasms/epidemiology , Soft Tissue Neoplasms/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Antigens, CD34/genetics , Child , Dermatofibrosarcoma/diagnosis , Dermatofibrosarcoma/pathology , Facial Neoplasms/diagnosis , Facial Neoplasms/pathology , Female , Humans , Infant , Male , Middle Aged , Nigeria/epidemiology , Sex Distribution , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , Soft Tissue Neoplasms/diagnosis , Soft Tissue Neoplasms/pathology , Young Adult
7.
Article in English | AIM (Africa) | ID: biblio-1266969

ABSTRACT

Objective: Chondromas are benign intraosseous cartilaginous tumors composed of mature hyaline cartilage; they may however arise from the soft tissue in rare cases without bone or joint involvement and are called extra skeletal or soft tissue chondromas. Extra skeletal chondromas (ESC) are commonly seen in the hands and feet but rarely in the oral cavity. We report a rare case of extra skeletal chondroma of the gingiva in a 31-year-old male patient following trauma to the anterior maxillary soft and hard tissues.Case Description: This is a case of a 31year old hypertensive patient with 3weeks history of gingival swelling in relation to the upper incisors which were fractured following an injury sustained from a motorbike fall. Clinical examination revealed a firm, non-tender localized gingival enlargement adjacent to the palatal surfaces of the maxillary incisors which had a lobulated appearance, with areas of inflammation that bled on gentle probing. The palatal gingival swelling was excised under local anesthesia, while gingivoplasty was performed on the labial gingiva of the same teeth. A periodontal dressing was placed on the surgical sites and removed at one-week review. Histopathologic examination of the palatal swelling revealed connective tissue that was densely infiltrated by mixed inflammatory cells. In some areas, there was focal chondroid tissue with chondrocytes of varying sizes in a chondromyxoid matrix.Conclusion: A rare case of extra skeletal chondroma is reported, we encourage report of more cases with long term follow-up in multicenter study among Nigerians, to ascertain the prevalence, gender, site of ESC in this population


Subject(s)
Gingivoplasty , Nigeria
8.
Contemp Clin Dent ; 8(4): 565-570, 2017.
Article in English | MEDLINE | ID: mdl-29326507

ABSTRACT

BACKGROUND: Long-term treatment of common chronic cardiac conditions such as hypertension with calcium channel blockers (CCBs) has long been associated with gingival hyperplasia. This oral side effect may affect esthetics and function, yet often overlooked and therefore underreported among Nigerians. AIM: This study aimed to determine the association of CCBs with gingival overgrowth (GO) in hypertensive patients. METHODS: This was a hospital-based, case-control study conducted among 116 hypertensive patients (58 CCB and 58 non-CCB age-matched controls) attending the medical outpatient clinic of a tertiary health institution in Lagos, Nigeria. Data collection tools included interviewer-administered questionnaires and periodontal examination. Sociodemographic details, medical history, and periodontal indices (gingival index, plaque index, class of GO according to drug-induced GO [DIGO] Clinical Index) were recorded. RESULTS: The mean age was 59.4 ± 12.6 years, females representing 50.9%. In the CCB group, 39 (67.2%) participants were on amlodipine and 19 (32.8%) were on nifedipine. The mean duration of CCB use was 55.6 ± 53 months. DIGO was higher in CCB (36.2%) than that in non-CCB participants (17.2%) (χ2 = 4.4, P = 0.036). The risk of GO was higher in CCB users (odds ratio [OR] 2.7, [95% confidence interval (CI)]: 1.1-6.5). Amlodipine users had higher DIGO (37.5%) than that of nifedipine users (21.1%) (OR 2.3, [95% CI]: 1.0-5.3). The predominant class of DIGO among the CCB users was Class 2 DIGO Clinical Index (90.5%). CONCLUSION: The study reveals that the risk of GO is nearly three times in CCB than that of non-CCB users and twice higher in amlodipine than nifedipine users in Nigeria.

9.
Pan Afr Med J ; 24: 102, 2016.
Article in English | MEDLINE | ID: mdl-27642441

ABSTRACT

INTRODUCTION: Adenomatoid odontogenic tumor (AOT) is a benign lesion originating from the dental lamina or its remnants. It is a relatively uncommon neoplasm representing about 3% of all odontogenic tumors. The aim of this study was to examine the clinical and radiological characteristics of AOTs in five major tertiary centres in Nigeria. METHODS: Archival hospital-based data stores of five tertiary health facilities in Nigeria were accessed. Case files and biopsy records were retrieved to obtain relevant information. Data was collected according to a proforma for standardization and entered into and analysed using SPSS for Windows (version 20.0; SPSS Inc. Chicago, IL). RESULTS: 61 (4.5%) cases of AOT were documented. The age range was 8-46 years with a mean age of 20.4±9.9 years. Male: Female ratio was 1:1.3. The anterior maxilla had 34 (55.8%) cases and the anterior mandible had 20 (32.8%) cases. 40 (65.6%) follicular cases, 20 (32.8%) extra-follicular cases and 1(1.6%) extra-osseous case were found. 31 cases (61.1%) were associated with impacted teeth and the upper canine was involved in 19 (57.6%) cases. CONCLUSION: This study showed AOT to be more common in the maxilla, more in females, most often associated with impacted canines, however, the suggestion of AOT being a "Two third tumour" was not observed in this study.


Subject(s)
Ameloblastoma/epidemiology , Mandibular Neoplasms/epidemiology , Maxillary Neoplasms/epidemiology , Adolescent , Adult , Ameloblastoma/pathology , Biopsy , Child , Female , Humans , Male , Mandibular Neoplasms/pathology , Maxillary Neoplasms/pathology , Middle Aged , Nigeria/epidemiology , Retrospective Studies , Sex Distribution , Young Adult
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