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1.
Dentomaxillofac Radiol ; 53(7): 439-446, 2024 Oct 01.
Article in English | MEDLINE | ID: mdl-38937280

ABSTRACT

OBJECTIVES: To develop and validate a modified deep learning (DL) model based on nnU-Net for classifying and segmenting five-class jaw lesions using cone-beam CT (CBCT). METHODS: A total of 368 CBCT scans (37 168 slices) were used to train a multi-class segmentation model. The data underwent manual annotation by two oral and maxillofacial surgeons (OMSs) to serve as ground truth. Sensitivity, specificity, precision, F1-score, and accuracy were used to evaluate the classification ability of the model and doctors, with or without artificial intelligence assistance. The dice similarity coefficient (DSC), average symmetric surface distance (ASSD), and segmentation time were used to evaluate the segmentation effect of the model. RESULTS: The model achieved the dual task of classifying and segmenting jaw lesions in CBCT. For classification, the sensitivity, specificity, precision, and accuracy of the model were 0.871, 0.974, 0.874, and 0.891, respectively, surpassing oral and maxillofacial radiologists (OMFRs) and OMSs, approaching the specialist. With the model's assistance, the classification performance of OMFRs and OMSs improved, particularly for odontogenic keratocyst (OKC) and ameloblastoma (AM), with F1-score improvements ranging from 6.2% to 12.7%. For segmentation, the DSC was 87.2% and the ASSD was 1.359 mm. The model's average segmentation time was 40 ± 9.9 s, contrasting with 25 ± 7.2 min for OMSs. CONCLUSIONS: The proposed DL model accurately and efficiently classified and segmented five classes of jaw lesions using CBCT. In addition, it could assist doctors in improving classification accuracy and segmentation efficiency, particularly in distinguishing confusing lesions (eg, AM and OKC).


Subject(s)
Cone-Beam Computed Tomography , Deep Learning , Cone-Beam Computed Tomography/methods , Humans , Sensitivity and Specificity , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/classification , Radiographic Image Interpretation, Computer-Assisted/methods , Jaw Diseases/diagnostic imaging , Jaw Diseases/classification
2.
Dentomaxillofac Radiol ; 53(5): 316-324, 2024 Jun 28.
Article in English | MEDLINE | ID: mdl-38627247

ABSTRACT

OBJECTIVES: Preoperative diagnosis of oral ameloblastoma (AME) and odontogenic keratocyst (OKC) has been a challenge in dentistry. This study uses radiomics approaches and machine learning (ML) algorithms to characterize cone-beam CT (CBCT) image features for the preoperative differential diagnosis of AME and OKC and compares ML algorithms to expert radiologists to validate performance. METHODS: We retrospectively collected the data of 326 patients with AME and OKC, where all diagnoses were confirmed by histopathologic tests. A total of 348 features were selected to train six ML models for differential diagnosis by a 5-fold cross-validation. We then compared the performance of ML-based diagnoses to those of radiologists. RESULTS: Among the six ML models, XGBoost was effective in distinguishing AME and OKC in CBCT images, with its classification performance outperforming the other models. The mean precision, recall, accuracy, F1-score, and area under the curve (AUC) were 0.900, 0.807, 0.843, 0.841, and 0.872, respectively. Compared to the diagnostics by radiologists, ML-based radiomic diagnostics performed better. CONCLUSIONS: Radiomic-based ML algorithms allow CBCT images of AME and OKC to be distinguished accurately, facilitating the preoperative differential diagnosis of AME and OKC. ADVANCES IN KNOWLEDGE: ML and radiomic approaches with high-resolution CBCT images provide new insights into the differential diagnosis of AME and OKC.


Subject(s)
Ameloblastoma , Cone-Beam Computed Tomography , Machine Learning , Odontogenic Cysts , Humans , Cone-Beam Computed Tomography/methods , Ameloblastoma/diagnostic imaging , Ameloblastoma/surgery , Ameloblastoma/pathology , Odontogenic Cysts/diagnostic imaging , Odontogenic Cysts/surgery , Retrospective Studies , Female , Male , Diagnosis, Differential , Adult , Middle Aged , Algorithms , Adolescent , Aged , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/surgery , Radiographic Image Interpretation, Computer-Assisted/methods , Radiomics
3.
Dentomaxillofac Radiol ; 53(7): 497-500, 2024 Oct 01.
Article in English | MEDLINE | ID: mdl-39087565

ABSTRACT

INTRODUCTION: Medication-related osteonecrosis of the jaw (MRONJ) and jaw metastasis might share similar clinical and radiographic characteristics, with both demonstrating F-18 fluorodeoxyglucose (FDG) uptake on PET-CT. Prostate-specific membrane antigen (PSMA) PET-CT is used to demonstrate prostate cancer dissemination. Unlike FDG PET-CT, PSMA PET-CT is more specific to cancer than to inflammation. Therefore, we hypothesized that it might be a useful tool to differentiate between MRONJ and jaw metastasis. METHODS: All files of prostate cancer patients diagnosed with MRONJ and with available PSMA PET-CT studies were retrieved. A similar number of solid cancer patients with MRONJ and with available FDG PET-CT studies served as a second study group. All studies were reviewed by 2 blinded co-investigators (L.D. and M.F.). RESULTS: Seventeen patients who underwent PSMA PET-CT (24 studies) and 15 patients who underwent FDG PET-CT (29 studies) met the inclusion criteria. All patients with FDG PET-CT studies showed pathological uptake at the site of MRONJ in at least one of their studies versus only 23.5% of patients in the PSMA PET-CT group (P < .001). FDG PET-CT studies showed pathological uptake in 89.6% of the studies compared with only 20.8% in the PSMA PET-CT group (P < .001). The mean standardized uptake value (SUVmax) and the mean uptake volume in the FDG PET-CT group were significantly higher compared with the PSMA PET-CT group (P < .001 and P < .005, respectively). The interclass correlation coefficient for all parameters was higher than 0.95. CONCLUSIONS: PSMA PET-CT is useful to differentiate between MRONJ and jaw metastasis.


Subject(s)
Bisphosphonate-Associated Osteonecrosis of the Jaw , Fluorodeoxyglucose F18 , Positron Emission Tomography Computed Tomography , Prostatic Neoplasms , Radiopharmaceuticals , Humans , Positron Emission Tomography Computed Tomography/methods , Male , Aged , Diagnosis, Differential , Prostatic Neoplasms/pathology , Prostatic Neoplasms/diagnostic imaging , Bisphosphonate-Associated Osteonecrosis of the Jaw/diagnostic imaging , Middle Aged , Jaw Neoplasms/diagnostic imaging , Aged, 80 and over , Retrospective Studies , Antigens, Surface
4.
J Transl Med ; 17(1): 56, 2019 02 27.
Article in English | MEDLINE | ID: mdl-30813941

ABSTRACT

BACKGROUND: Osteosarcoma (OS) is the most common cancer of bone. Jaw osteosarcoma (JOS) is rare and it differs from other OS in terms of the time of occurrence (two decades later) and better survival. The aim of our work was to develop and characterize specific mouse models of JOS. METHODS: Syngenic and xenogenic models of JOS were developed in mice using mouse (MOS-J) and human (HOS1544) osteosarcoma cell lines, respectively. An orthotopic patient-derived xenograft model (PDX) was also developed from a mandibular biopsy. These models were characterized at the histological and micro-CT imaging levels, as well as in terms of tumor growth and metastatic spread. RESULTS: Homogeneous tumor growth was observed in both the HOS1544 and the MOS-J JOS models by injection of 0.25 × 106 and 0.50 × 106 tumor cells, respectively, at perimandibular sites. Histological characterization of the tumors revealed features consistent with high grade conventional osteosarcoma, and the micro-CT analysis revealed both osteogenic and osteolytic lesions. Early metastasis was encountered at day 14 in the xenogenic model, while there were no metastatic lesions in the syngenic model and in the PDX models. CONCLUSION: We describe the first animal model of JOS and its potential use for therapeutic applications. This model needs to be compared with the usual long-bone osteosarcoma models to investigate potential differences in the bone microenvironment.


Subject(s)
Jaw Neoplasms/pathology , Osteosarcoma/pathology , Xenograft Model Antitumor Assays , Animals , Cell Line, Tumor , Cell Proliferation , Female , Humans , Jaw Neoplasms/diagnostic imaging , Lung Neoplasms/secondary , Mandible/diagnostic imaging , Mandible/pathology , Mice, Inbred C57BL , Mice, SCID , Osteosarcoma/diagnostic imaging , Tumor Burden , X-Ray Microtomography
5.
J Oral Pathol Med ; 47(2): 192-197, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29121421

ABSTRACT

BACKGROUND: Glandular odontogenic cyst (GOC) demonstrates a significant predilection toward localized biologic aggressiveness and recurrence. GOC shares certain histopathologic features with intraosseous mucoepidermoid carcinoma (IMEC). The current investigation evaluates a group of recurrent, biologically aggressive GOCs to determine whether any cases demonstrated unique histologic features or mastermind-like2 (MAML2) rearrangements common to IMEC. METHODS: Microscopic slides from 11 previously diagnosed GOCs were stained with hematoxylin and eosin and assessed by 2 study participants for 10 classic histopathologic features required to establish a diagnosis of GOC. Cases were evaluated utilizing break-apart fluorescent in situ hybridization (FISH) analysis for the presence of MAML2 gene rearrangements. Clinical and demographic data on all patients were recorded. RESULTS: The mean age for patients included in the study was 55.27 years with a range of 36 to 72 years. The most common presenting symptom was a jaw expansion, and all cysts presented initially as a unilocular or multilocular radiolucency. Cysts displayed a minimum of 6 of 10 histologic parameters necessary for a diagnosis of GOC. One case demonstrated MAML2 rearrangements by FISH. That case also showed marked ciliation of cyst-lining epithelial cells and extensive mucous-secreting goblet cell proliferation. CONCLUSION: Findings in the current study are in concert with previous investigations, and although this study finds only limited molecular evidence to support the premise that recurrent biologically aggressive GOCs are a precursor to IMEC, detection of MAML2 rearrangements in 1 case suggests that such a theoretic transition, while rare, is possible.


Subject(s)
Carcinoma, Mucoepidermoid/genetics , Carcinoma, Mucoepidermoid/pathology , DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Gene Rearrangement , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , Odontogenic Cysts/genetics , Odontogenic Cysts/pathology , Transcription Factors/genetics , Transcription Factors/metabolism , Adult , Aged , Biomarkers, Tumor/genetics , Epithelial Cells/pathology , Female , Humans , In Situ Hybridization, Fluorescence , Jaw Diseases/genetics , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/genetics , Keratins/metabolism , Male , Mandible/diagnostic imaging , Mandible/pathology , Maxilla/diagnostic imaging , Maxilla/pathology , Middle Aged , Neoplasm Recurrence, Local/genetics , Odontogenic Cysts/diagnostic imaging , Radiography , Trans-Activators
6.
Oral Dis ; 24(3): 307-316, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28142213

ABSTRACT

Ameloblastoma is a benign odontogenic tumor of epithelial origin. It is locally aggressive with unlimited growth capacity and has a high potential for malignant transformation as well as metastasis. Ameloblastoma has no established preventive measures although majority of patients are between ages 30 and 60 years. Molecular and genetic factors that promote oncogenic transformation of odontogenic epithelium to ameloblastoma are strongly linked to dysregulation of multiple genes associated with mitogen-activated protein kinase, sonic hedgehog, and WNT/ß-catenin signaling pathways. Treatment of ameloblastoma is focused on surgical resection with a wide margin of normal tissue because of its high propensity for locoregional invasion; but this is often associated with significant patient morbidity. The relatively high recurrence rate of ameloblastoma is influenced by the type of molecular etiological factors, the management approach, and how early the patient presents for treatment. It is expected that further elucidation of molecular factors that orchestrate pathogenesis and recurrence of ameloblastoma will lead to new diagnostic markers and targeted drug therapies for ameloblastoma.


Subject(s)
Ameloblastoma , Jaw Neoplasms , Ameloblastoma/diagnostic imaging , Ameloblastoma/etiology , Ameloblastoma/pathology , Ameloblastoma/therapy , Humans , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/etiology , Jaw Neoplasms/pathology , Jaw Neoplasms/therapy , Neoplasm Recurrence, Local
7.
Oral Dis ; 24(1-2): 63-66, 2018 Mar.
Article in English | MEDLINE | ID: mdl-29480593

ABSTRACT

Ameloblastoma are the most common odontogenic tumor. As they usually do not form metastasis, they are considered as benign tumors with a locally invasive growth pattern and destruction of the jaws and the surrounding tissue (Oral Diseases, 23, 2017, 199). This article focuses on clinical, radiological, and therapeutic findings, which may influence diagnosis and treatment of ameloblastoma in the future.


Subject(s)
Ameloblastoma/genetics , Ameloblastoma/therapy , Jaw Neoplasms/genetics , Jaw Neoplasms/therapy , Molecular Targeted Therapy , Ameloblastoma/diagnostic imaging , Ameloblastoma/pathology , Humans , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/pathology
8.
J Oral Maxillofac Surg ; 76(11): 2348-2359, 2018 11.
Article in English | MEDLINE | ID: mdl-29859157

ABSTRACT

PURPOSE: The aims of this study were to describe the clinical and radiologic features of 383 fibro-osseous lesions (FOLs) from an oral pathology reference service in Brazil and to compare the findings with previous studies. The hypothesis of the study was that the most common type of FOL would differ from other investigations. MATERIALS AND METHODS: We conducted a descriptive and retrospective study with review of the records of the clinical and biopsy services (1990 to 2015). All records of the patients included showed a definitive diagnosis of FOL. The primary outcome variable was the type of FOL, and the predictor variables were gender, age, ethnicity, location, and clinical and radiologic characteristics. Descriptive analyses and χ2 tests were performed. The P value was set at .05. RESULTS: From the 27,998 records available, 383 showed FOLs, with 187 (48.8%) being cemento-osseous dysplasias (CODs), 103 (26.9%) being fibrous dysplasias (FDs), and 93 (24.3%) being ossifying fibromas (OFs). The mean age of the patients was 38.5 ± 17.5 years. CODs presented a predilection for female gender (n = 314, 82.0%), African descent (n = 134, 71.6%), and the mandible (n = 248, 64.6%). The most common radiologic feature was a mixed radiolucent-radiopaque image (n = 149, 51.7%). FDs and OFs were commonly diagnosed during the first and second decades of life (P < .001), whereas CODs were more frequently diagnosed beyond the third decade (P < .001). Secondary osteomyelitis was more significantly observed in CODs (P < .001) than in FDs and OFs. Swelling was more frequently reported for FDs and OFs than for CODs (P < .001). CONCLUSIONS: CODs were the most frequently observed FOLs in this Brazilian population. Female patients, patients of African descent, and patients with mandibular localization were most commonly affected by these conditions. The most common type of FOL differed from that in similar case reports or series from various geographic locations. It is believed that the data source (clinical and/or biopsy services) can directly influence the outcome.


Subject(s)
Cementoma/pathology , Fibroma, Ossifying/pathology , Fibrous Dysplasia of Bone/pathology , Jaw Diseases/pathology , Jaw Neoplasms/pathology , Adolescent , Adult , Brazil , Cementoma/diagnostic imaging , Child , Diagnosis, Differential , Female , Fibroma, Ossifying/diagnostic imaging , Fibrous Dysplasia of Bone/diagnostic imaging , Humans , Jaw Diseases/diagnostic imaging , Jaw Neoplasms/diagnostic imaging , Male , Middle Aged , Radiography, Panoramic , Retrospective Studies
9.
J Xray Sci Technol ; 26(1): 133-140, 2018.
Article in English | MEDLINE | ID: mdl-29480235

ABSTRACT

Cone beam computed tomography (CBCT) has obvious advantages over regular radiography in diagnosis of complex diseases. Objective of this study is to report a case of a mandibular jaw ameloblastoma recurring cyst, which represents a benign tumor of odontogenic epithelium, using CBCT imaging technology. CBCT examination of the patient suffering with recurrent lower jaw cyst (relapsing four years after surgery) showed a decrease in irregular bone density and appearance of a honeycomb pattern (3.5 cm×2.5 cm×1.8 cm) in the right lower jaw. This suggests that the lesion is more likely to be an ameloblastoma. Preoperative tissue biopsy and pathological examination of surgical sample confirmed the diagnosis. Surgical resection of the diseased tissue and autogenous bone grafting in the mandible was performed. Postoperative CBCT examination showed that the bone defect healed well, without recurrence of the tumor 22 months postoperatively. In conclusion, the rotated 3D CBCT images clearly displays the exact size, location, borders and internal changes of the tumor in the jaw cyst itself and the adjacent tissues. Thus, the dental CBCT allows clinicians to better evaluate lesions, leading to better treatment outcomes.


Subject(s)
Ameloblastoma/diagnostic imaging , Cone-Beam Computed Tomography/methods , Imaging, Three-Dimensional/methods , Jaw Neoplasms/diagnostic imaging , Adult , Ameloblastoma/surgery , Female , Humans , Jaw Neoplasms/surgery , Mandible/diagnostic imaging , Mandible/surgery , Tooth/diagnostic imaging , Tooth/surgery
10.
Mod Pathol ; 30(s1): S96-S103, 2017 01.
Article in English | MEDLINE | ID: mdl-28060370

ABSTRACT

Odontogenic cysts and osseous lesions are often seen as challenging diagnostic lesions but the majority of them are easily classified. This article outlines the diagnostic features required for separating the most common of odontogenic cysts and select osseous lesions of the jaws. Clinical and radiographic findings of these jaw lesions often lead to a differential diagnosis that only the histologic findings will clarify. Dentigerous cyst, keratocystic odontogenic tumor, and certain ameloblastomas that have cystic change, may have identical radiographic findings, with only separation by their specific histologic features leading to the significantly different treatments required for each. Conversely, some cystic lesions can appear histologically identical and cannot be diagnosed without the radiographic findings. Certain osseous lesions of the jaws are particularly problematic for diagnosis without the appropriate radiographic findings, and the diagnosis should probably not be attempted on the histologic findings alone. This article will integrate the necessary clinical, radiographic, and histologic findings required to address the most common odontogenic lesions.


Subject(s)
Jaw Cysts/diagnosis , Jaw Neoplasms/diagnosis , Odontogenic Tumors/diagnosis , Diagnosis, Differential , Humans , Jaw Cysts/diagnostic imaging , Jaw Cysts/pathology , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/pathology , Odontogenic Tumors/diagnostic imaging , Odontogenic Tumors/pathology
11.
Am J Emerg Med ; 35(5): 805.e1-805.e2, 2017 May.
Article in English | MEDLINE | ID: mdl-28041759

ABSTRACT

Numb chin syndrome (NCS) is a rare yet potentially ominous sensory neuropathy in the distribution of the mental or inferior alveolar nerve characterized by unilateral hypoesthesia over the lower lip, chin and occasionally gingival mucosa. Recognizing NCS is clinically important as this may be a subtle sign of occult malignancy progression or heralding the relapses. It may also occur in benign disease, both systemic and dental in origin. Current expert opinion is that patients with NCS without apparent cause should be assumed to have a malignant etiology until proven otherwise Lossos and Siegal (1992) [1]. Here we report a relapse of Non-Hodgkin lymphoma with NCS with no evidence of metastasis.


Subject(s)
Chin/pathology , Hypesthesia/diagnostic imaging , Jaw Neoplasms/secondary , Lymphoma, Non-Hodgkin/pathology , Diagnosis, Differential , Disease Progression , Humans , Hypesthesia/pathology , Jaw Neoplasms/diagnostic imaging , Lymphoma, Non-Hodgkin/complications , Lymphoma, Non-Hodgkin/diagnostic imaging , Male , Middle Aged , Recurrence , Syndrome
12.
J Craniofac Surg ; 28(5): 1197-1205, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28538076

ABSTRACT

Cysts and tumors are common lesions in the jaws. To be able to retain a good volume of the alveolar ridge during healing as well as strengthening the angle and body of the mandible and provide an instant improved support for adjacent teeth, reliable long-term bone regeneration is needed. The purpose of this prospective study was to promote bone regeneration by filling bony defects in the upper or lower jaw with granules of the bioactive glass S53P4 (BAG), which have osteostimulative and antimicrobial properties.The authors treated 20 patients (21 defects) surgically; benign tumors, cysts, or infection related to impacted teeth in the maxilla or mandible. The tumor or cyst was removed or enucleated and thorough cleaning of the infected area was performed. The bone cavity was filled with granules of the BAG S53P4 despite signs of chronic infection in the area at the time of surgery. The patients were followed up for an average of 34 months clinically and with cone beam computerized tomography for 28 months. In 20 defects the final outcome was successful. Despite infection at the time of surgery in 65% of the patients, no material associated infection was seen during the follow-up. The BAG S53P4 granules were radiologically remodeled into bone after 2 years follow-up. The use of granules of the BAG S53P4 in the treatment of large bone defects provides infection-free reliable bone regeneration despite chronic infection at the time of surgery, which improves the prognosis of adjacent teeth.


Subject(s)
Ameloblastoma/diagnostic imaging , Ameloblastoma/surgery , Bone Substitutes , Dentigerous Cyst/surgery , Glass , Jaw Cysts/surgery , Jaw Neoplasms/surgery , Mandible/surgery , Maxilla/surgery , Osteomyelitis/surgery , Tooth, Impacted/surgery , Adult , Cone-Beam Computed Tomography , Dentigerous Cyst/diagnostic imaging , Female , Follow-Up Studies , Humans , Jaw Cysts/diagnostic imaging , Jaw Neoplasms/diagnostic imaging , Male , Mandible/diagnostic imaging , Maxilla/diagnostic imaging , Middle Aged , Osteomyelitis/diagnostic imaging , Postoperative Complications/diagnostic imaging , Tooth, Impacted/diagnostic imaging , Young Adult
13.
Rev Med Liege ; 72(7-8): 344-348, 2017 Jul.
Article in French | MEDLINE | ID: mdl-28795546

ABSTRACT

Ameloblastoma is an odontogenic tumour that represents 1 % of oral tumours but 10 % of odontogenic tumours. Ameloblastoma is characterized by low and noiseless growth, that explains a lot of advanced forms. The tumour is known as benign with local malignity due to its locally invasive behaviour and its recurrence. The treatment choice remains complicated because of recurring nature and large resection in vital anatomical areas. The therapeutic approach will be based on size, anatomical localisation, histologic variants and anatomical complications. The treatment options should be discussed with the patient because of possible important morphological and functional sequelae.


L'améloblastome est une tumeur odontogène qui représente 1 % des tumeurs orales, mais 10 % des tumeurs odontogènes. L'améloblastome se caractérise par une croissance lente à bas bruit, ce qui peut expliquer la fréquence de formes étendues. La tumeur est dite bénigne à malignité locale, suite à son comportement invasif localement et sa forte propension à la récidive. La décision du type de traitement reste compliquée étant donné son caractère récidivant et ses difficultés de résection large dans des zones anatomiques vitales. L'approche thérapeutique se basera sur la taille et la localisation ainsi que sur ses variantes histologiques et ses complications anatomiques. Elle sera discutée avec le patient car ce dernier peut subir des séquelles morphologiques et fonctionnelles importantes.


Subject(s)
Ameloblastoma/diagnostic imaging , Central Nervous System Cysts/complications , Eye Abnormalities/complications , Fingers/abnormalities , Jaw Neoplasms/diagnostic imaging , Skin Abnormalities/complications , Ameloblastoma/pathology , Ameloblastoma/surgery , Humans , Jaw Neoplasms/pathology , Jaw Neoplasms/surgery , Male , Young Adult
14.
J Oral Pathol Med ; 45(8): 599-604, 2016 Sep.
Article in English | MEDLINE | ID: mdl-26822069

ABSTRACT

BACKGROUND: Odontogenic myxoma is a benign, locally aggressive neoplasm of the jaws. Prevalence rates range between 0.5% and 17.7% of odontogenic tumours. There are few reports in the literature on this lesion in African populations, and therefore, this study aimed to report on odontogenic myxoma in a South African population over a 40-year period. METHODS: The clinical records and orthopantomograms of 29 histopathologically diagnosed odontogenic myxoma were retrospectively analysed. Details of age, gender, ethnic origin and clinical, histological as well as radiological features were recorded. RESULTS: The ages of patients ranged from 7 to 44 years with a mean of 21.3 years. The male-to-female ratio was 1:2.6 with the majority of patients being of mixed race and Africans. Clinically, 31% complained of pain while 58.6% had a history of swelling. The majority of odongenic myxomas (62.1%) were located in the mandible with the posterior region being most commonly affected. Multilocular lesions (69.2%) were more common and were significantly larger than unilocular lesions (P < 0.05). The outline of these tumours was mostly well-defined (84.6%) with different degrees of cortication. Only one tumour caused tooth resorption, while 20 cases (76.9%) caused tooth displacement. Six tumours expanded into the maxillary sinus, and 14 tumours caused expansion of the mandible. CONCLUSIONS: Odontogenic myxomas have variable clinical, radiological and histological features. Most of these features in this population were similar to other populations. It is mandatory to use conventional radiographs along with histopathological examination to aid in arriving at an accurate diagnosis.


Subject(s)
Jaw Neoplasms/pathology , Myxoma/pathology , Odontogenic Tumors/pathology , Adolescent , Adult , Child , Female , Humans , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/epidemiology , Male , Mandible/diagnostic imaging , Mandibular Neoplasms/diagnostic imaging , Mandibular Neoplasms/epidemiology , Mandibular Neoplasms/pathology , Maxillary Neoplasms/diagnostic imaging , Maxillary Neoplasms/epidemiology , Maxillary Neoplasms/pathology , Myxoma/diagnostic imaging , Myxoma/epidemiology , Odontogenic Tumors/diagnostic imaging , Odontogenic Tumors/epidemiology , Prevalence , Retrospective Studies , South Africa/epidemiology , Young Adult
15.
J Oral Maxillofac Surg ; 74(5): 973-81, 2016 May.
Article in English | MEDLINE | ID: mdl-26679553

ABSTRACT

PURPOSE: Primary Ewing sarcoma of the jaw is rare. The aim of this study was to describe new cases of primary Ewing sarcoma of the jaw and investigate reported prognostic factors of Ewing sarcoma in this series and treatment outcome. MATERIALS AND METHODS: Six patients with primary Ewing sarcoma of the jaw were treated at the Memorial Sloan Kettering Cancer Center (MSKCC) from 1992 through 2013. Clinical data, pathology reports, treatment prescribed, treatment regimens, outcome, and follow-up information were reviewed. RESULTS: Five of 6 patients were female and 5 cases were in the mandible. No patient presented with metastatic disease at diagnosis. All cases were positive for CD99, and 3 patients with genetic confirmation were positive for EWS-FLI1 fusion or EWSR1 gene rearrangement. All patients received induction multiagent chemotherapy and surgical resection and 2 patients received adjuvant radiotherapy. Total (grade IV) or nearly total (grade III) tumor necrosis in 3 of 5 patients (60%) assessed for histologic response to chemotherapy indicated intense sensitivity. All patients were alive and free of disease, with no history of local recurrence, at a median follow-up period of 6.5 years. CONCLUSION: Patients with primary Ewing sarcoma of the jaw have a good prognosis and metastasis is an uncommon occurrence at initial presentation.


Subject(s)
Bone Neoplasms/diagnosis , Jaw Neoplasms/diagnosis , Sarcoma, Ewing/diagnosis , Adolescent , Bone Neoplasms/therapy , Child , Child, Preschool , Female , Humans , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/therapy , Male , Prognosis , Retrospective Studies , Sarcoma, Ewing/diagnostic imaging , Sarcoma, Ewing/therapy , Survival Analysis , Tomography, X-Ray Computed , Treatment Outcome , Young Adult
16.
Am J Otolaryngol ; 37(4): 362-4, 2016.
Article in English | MEDLINE | ID: mdl-27038821

ABSTRACT

OBJECTIVES: The aims of this study are to describe the radiological appearance of two common odontogenic lesions (keratocystic odontogenic tumor and ameloblastoma) arising in the same patient simultaneously with their radiological differences and histological correlates, and to describe challenges in radiological diagnosis. DESIGN: Single case report. SETTING: Tertiary referral center. PARTICIPANTS: Forty-one year-old African-American male patient. MAIN OUTCOME MEASURE: Lesion appearance on computed tomography (CT) scan and pathological correlates. RESULTS: A 41year-old African-American male presented with asymptomatic right maxillary swelling. A CT scan of the maxillofacial skeleton showed and expansile and cystic lesion of the right hemimaxilla with trabecular osseous expansion, and a left cystic lesion in the left hemimaxilla expanding into the pterygopalatine fossa. Biopsy confirmed the suspected diagnoses of right ameloblastoma and left keratocystic odontogenic tumor. CONCLUSION: Although they are among the most common odontogenic tumors, the presence of concurrent ameloblastoma and KOT is an exceedingly rare occurrence in the same patient. The appearance on CT scan may help in distinguishing ameloblastoma from KOT by looking at bone expansion and high density areas, although the gold standard diagnostic test remains open biopsy.


Subject(s)
Ameloblastoma/diagnostic imaging , Jaw Neoplasms/diagnostic imaging , Odontogenic Tumors/diagnostic imaging , Adult , Diagnosis, Differential , Humans , Male , Tomography, X-Ray Computed
17.
Clin Radiol ; 70(1): 25-36, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25439185

ABSTRACT

During the last decade much has changed in our understanding of fibro-osseous lesions (FOLs) of the jaws with regards to their imaging, their nomenclature and classification, and their potential impact on the overall health of the patient. The changes in nomenclature, classification, and the FOLs' potential association with important syndromes are discussed with the assistance of a flowchart. The lesions, fibrous dysplasia (FD), ossifying fibroma (OF), and osseous dysplasia (OD), though with similar histopathology, have very different clinical and radiological presentations, behaviour, and treatment outcomes. FD of the jaw, which though becoming inactive, does not involute and therefore requires life-long review to monitor for occasional reactivation. OF is completely removed surgically as it has a propensity to recur. No treatment is generally required for an OD unless it is infected or displays expansion. Lesions outside the jaws associated with FOLs of the jaws are identified. Radiology remains central to the diagnosis of FOLs of the jaw, because the pathologist is still not able to distinguish between them. The advent of cone-beam computed tomography (CBCT) with its better radiation dose reduction, accessibility, and spatial resolution has transformed imaging of FOLs. Their presentations on CBCT and the clinical indications for its use are discussed.


Subject(s)
Cone-Beam Computed Tomography/methods , Fibroma, Ossifying/diagnostic imaging , Fibrous Dysplasia of Bone/diagnostic imaging , Jaw Neoplasms/diagnostic imaging , Diagnosis, Differential , Humans , Risk Factors
18.
Clin Radiol ; 70(4): 335-50, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25559378

ABSTRACT

There is a wide range of pathological conditions that affect the mandible. Although some lesions demonstrate characteristic imaging features, many of the pathological processes encountered in the mandible often exhibit similar imaging appearances resulting in uncertainty for the reporting radiologist. Many mandibular lesions remain impossible to distinguish without histological analysis. Therefore, this review aims to reassure the radiologist that although imaging findings may not always lead to a specific diagnosis, they narrow the differential diagnosis and guide further work-up. In this regard, we aim to provide a clinically useful framework and approach for radiologists to use when they encounter lesions within the mandible.


Subject(s)
Jaw Cysts/diagnostic imaging , Jaw Neoplasms/diagnostic imaging , Mandible/diagnostic imaging , Diagnosis, Differential , Humans , Magnetic Resonance Imaging , Odontogenic Tumors/diagnostic imaging , Tomography, X-Ray Computed/methods
20.
Vet Radiol Ultrasound ; 55(2): 147-58, 2014.
Article in English | MEDLINE | ID: mdl-24102949

ABSTRACT

Odontogenic neoplasms are locally invasive oral tumors in dogs. The purpose of this retrospective study was to describe CT characteristics for varying histopathologic types of canine odontogenic neoplasms. A board-certified veterinary radiologist who was unaware of histologic findings reviewed and scored imaging studies. A total of 29 dogs were included in the study. Twenty-three of these dogs had concurrent dental radiographs. The most common CT characteristics for all tumor types were a direct association with or in the region of multiple teeth in 96.4% (27/28), contrast enhancement in 96.3% (26/27), alveolar bone lysis in 93.1% (27/29), and mass-associated tooth displacement in 85.2% (23/27). Mass-associated cyst-like structures were identified in 53.6% (15/28) and were only present in tumors containing odontogenic epithelium. Canine acanthomatous ameloblastomas (n = 15) appeared as extra-osseous (10/15) or intra-osseous (5/15) masses. Intra-osseous canine acanthomatous ameloblastomas were more likely to have mass-associated cyst-like structures and were subjectively more aggressive when compared with extra-osseous canine acanthomatous ameloblastomas. Amyloid-producing odontogenic tumors (n = 3) had subjectively uniform CT imaging characteristics and consisted of round soft tissue and mineral attenuating masses with multiple associated cyst-like structures. Fibromatous epulides of periodontal ligament origin (n = 4) were contrast enhancing extra-osseous masses that were rarely referred for CT examinations and 25% (1/4) were not visible with CT. Other odontogenic tumors were less represented or had more variable CT imaging characteristics. Mass-associated tooth destruction was appreciated more often with dental radiographs and extra-oral tumor extension was identified more often with CT.


Subject(s)
Dog Diseases/diagnostic imaging , Jaw Neoplasms/veterinary , Odontogenic Tumors/veterinary , Ameloblastoma/classification , Ameloblastoma/diagnostic imaging , Ameloblastoma/pathology , Ameloblastoma/veterinary , Animals , Dog Diseases/classification , Dog Diseases/pathology , Dogs , Female , Jaw Neoplasms/classification , Jaw Neoplasms/diagnostic imaging , Jaw Neoplasms/pathology , Male , Odontogenic Tumors/classification , Odontogenic Tumors/diagnostic imaging , Odontogenic Tumors/pathology , Retrospective Studies , Tomography, X-Ray Computed/veterinary
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