keyword
https://read.qxmd.com/read/24950870/-oral-and-stomatological-pathology-case-6-ameloblastic-fibroma
#41
JOURNAL ARTICLE
Michel Wassef
No abstract text is available yet for this article.
June 2014: Annales de Pathologie
https://read.qxmd.com/read/24574665/ameloblastic-fibrosarcoma-report-of-a-case
#42
JOURNAL ARTICLE
Akindayo O Akinyamoju, Adeola A Olusanya, Bukola F Adeyemi, B Kolude
Ameloblastic fibrosarcoma (AFS) is a rare odontogenic malignancy with benign epithelial and malignant ectomesenchymal components. About 66 cases have been reported in the medical literature. We therefore report an additional case as well as a review of literature to add to the existing knowledge on this rare lesion.
September 2013: Journal of Oral and Maxillofacial Pathology: JOMFP
https://read.qxmd.com/read/23878574/ameloblastic-fibrosarcoma-of-the-upper-jaw-report-of-a-rare-case-with-long-term-follow-up
#43
Maryam Khalili, Pouyan Amini Shakib
Ameloblastic fibrosarcoma (AFS) is a rare malignant mixed odontogenic tumor which is usually considered as the malignant counterpart of ameloblastic fibroma. Only mesenchymal component represents sarcomatous alterations and ameloblast-like epithelial nest remains bland in AFS. Here, we report a case of AFS in a 26-year-old man in the maxilla, which was regarded as an uncommon location for this tumor. After 2 years follow up, no evidence of recurrence was noted. We also emphasize on comprehensive clinical, radiographic, and histopathologic evaluation of such patients rather than immunohistochemical staining to make an accurate diagnosis...
January 2013: Dental Research Journal
https://read.qxmd.com/read/23845294/ameloblastic-fibrosarcoma-a-rare-malignant-odontogenic-tumor
#44
JOURNAL ARTICLE
S M Gilani, A Raza, B M Al-Khafaji
INTRODUCTION: Ameloblastic fibrosarcoma (AFS) is a rare malignant odontogenic tumor. It can arise de novo, however one-third of cases may arise from a recurrent ameloblastic fibroma, in which case they appear to present at an older age. CASE REPORT: A 16-year-old female presented with one month history of right mandibular mass. Computerized tomography (CT) scan showed a large destructive mass. A biopsy of the mass was performed. Histologically, it consisted of a mixed epithelial-mesenchymal odontogenic neoplasm composed of benign islands of well-differentiated ameloblastic epithelium within a malignant fibrous stroma consisting of spindle cells or fibroblasts with a brisk mitotic activity...
February 2014: European Annals of Otorhinolaryngology, Head and Neck Diseases
https://read.qxmd.com/read/23762647/recurrent-ameloblastic-fibroma-report-of-a-rare-case
#45
JOURNAL ARTICLE
Ravikumar S Kulkarni, Amitabh Sarkar, Sandeep Goyal
Ameloblastic fibroma (AF) is an uncommon mixed neoplasm of odontogenic origin frequently seen in the second decade of life. It mainly presents as an intrabony lesion but can even occur peripherally. Histologically, our case showed hypercellular areas, an uncommon feature seen in typical AF. Whether this benign lesion is treated by mode of enucleation and curettage or by extensive surgery is still a topic of debate. An extensive surgical treatment is suggested as the initial approach due to its high recurrence rate (18%) and the greater chances of recurrent AFs transforming into ameloblastic fibrosarcoma (45%), together with a long-term followup...
2013: Case Reports in Dentistry
https://read.qxmd.com/read/23730931/malignant-odontogenic-tumors-a-multicentric-latin-american-study-of-25-cases
#46
REVIEW
M Martínez Martínez, A Mosqueda-Taylor, R Carlos, W Delgado-Azañero, O P de Almeida
OBJECTIVE: The aim of this study was to show the epidemiological features of 25 malignant odontogenic tumors (MOT) in Latin America. MATERIALS AND METHODS: We retrieved 25 cases of MOT out of 2142 odontogenic tumors, from four oral diagnostic centers in Latin America, and described the main clinical and pathological characteristics. RESULTS: A total of 19 cases were carcinomas, including eight ameloblastic carcinomas, five primary intra-osseous squamous cell carcinomas, three clear cell odontogenic carcinomas and three ghost cell odontogenic carcinomas...
May 2014: Oral Diseases
https://read.qxmd.com/read/22924135/ameloblastic-fibroodontoma-of-the-mandible-with-normal-karyotype-in-a-pediatric-patient
#47
JOURNAL ARTICLE
Esther Manor, Elena Kan, Lipa Bodner
Background. Ameloblastic fibroodontoma (AFO) is a rare mixed odontogenic tumor with epithelial and mesenchymal components. AFO presents as a painless swelling in the mandible or maxilla. Radiographs show a well-defined radiolucent area containing various amounts of radiopaque material of irregular size and form. The common treatment is enucleation. It is not an aggressive tumor but recurrence and malignant transformation are possible. Methods. An AFO of the mandible of a 3-year-old female is reported. Panoramic radiograph and CT scan revealed a unilocular lesion with radiopaque center and radiolucent margins...
2012: Case Reports in Dentistry
https://read.qxmd.com/read/22557908/aggressive-atypical-ameloblastic-fibrodentinoma-report-of-a-case
#48
JOURNAL ARTICLE
Girish B Giraddi, Vipul Garg
Ameloblastic fibroma and related lesions constitute a group of lesions, which range in biologic behaviour from true neoplasms to hamartomas. This group of lesions is also sometimes referred to as mixed odontogenic tumors and usually includes ameloblastic fibroma, ameloblastic fibrodentinoma and ameloblastic fibro-odontoma. Despite numerous efforts however, there is still considerable confusion concerning the nature and interrelationship of these mixed odontogenic tumors and related lesions. The malignant counterpart of these lesions namely aameloblastic fibrosarcoma, ameloblastic dentinosarcoma and ameloblastic odontosarcoma respectively are said to arise secondarily in their benign counterpart or de novo...
January 2012: Contemporary Clinical Dentistry
https://read.qxmd.com/read/22542333/ameloblastic-fibrosarcoma-of-the-mandible-treatment-long-term-follow-up-and-subsequent-reconstruction-of-a-case
#49
JOURNAL ARTICLE
Roseanna Noordhoek, Marvin E Pizer, Daniel M Laskin
No abstract text is available yet for this article.
December 2012: Journal of Oral and Maxillofacial Surgery
https://read.qxmd.com/read/22177804/ameloblastic-fibrosarcoma-report-of-a-case-study-of-immunophenotype-and-comprehensive-review-of-the-literature
#50
REVIEW
Jonathan Lai, Nick Blanas, Kevin Higgins, Hagen Klieb
No abstract text is available yet for this article.
August 2012: Journal of Oral and Maxillofacial Surgery
https://read.qxmd.com/read/22082131/loss-of-heterozygosity-loh-in-tumour-suppressor-genes-in-benign-and-malignant-mixed-odontogenic-tumours
#51
JOURNAL ARTICLE
Clarice F Galvão, Carolina C Gomes, Marina G Diniz, Pablo A Vargas, Alfredo M B de Paula, Adalberto Mosqueda-Taylor, Adriano M Loyola, Ricardo S Gomez
Although molecular alterations are reported in different types of odontogenic tumours, their pathogenesis remains to be established. Loss of heterozygosity (LOH) studies allow the identification of minimal regions of deletions of known or putative tumour suppressor genes, the losses of which may promote neoplastic growth. The purpose of this study was to investigate LOH in a set of odontogenic mixed tumours. Tumour suppressor gene loci on 3p, 9p, 11p, 11q and 17p chromosomes were analysed in five samples of ameloblastic fibroma (AF), three samples of ameloblastic fibro-odontoma (AFO) and three samples of ameloblastic fibrosarcoma (AFS)...
May 2012: Journal of Oral Pathology & Medicine
https://read.qxmd.com/read/22029985/case-records-of-the-massachusetts-general-hospital-case-33-2011-a-56-year-old-man-with-hypophosphatemia
#52
JOURNAL ARTICLE
Clemens Bergwitz, Michael T Collins, Ravi S Kamath, Andrew E Rosenberg
Presentation of Case. Dr. Eric Hesse (Harvard School of Dental Medicine): A 56-year-old man was seen in the outpatient endocrinology and oral-surgery clinics of this hospital because of recurrent hypophosphatemia. The patient had been well until 19 years earlier, when rib pain developed and a left..
October 27, 2011: New England Journal of Medicine
https://read.qxmd.com/read/22009005/ameloblastic-fibrosarcoma-of-the-mandible-report-of-2-chemosensitive-pediatric-cases
#53
JOURNAL ARTICLE
Charlotte Demoor-Goldschmidt, Veronique Minard-Colin, Elizabeth Cassagneau, Stephane Supiot, Odile Oberlin, Cedric D'hautuille, Nadege Corradini
Ameloblastic fibrosarcoma (AFS) is a rare malignant odontogenic tumor. We report 2 pediatric cases of AFS from 2 different centers but reviewed by the same pathologist, which were unusual in that they were chemosensitive. Management was wide surgical resection, chemotherapy, and adjuvant radiotherapy. One case was a local AFS recurrence after incomplete surgery and the other was an AFS that was overlooked during earlier diagnosis of an ameloblastic fibroma. Both tumors responded very well to preoperative chemotherapy, with a reduction in tumor size and histologically proven decrease in viable tumor cell number...
March 2012: Journal of Pediatric Hematology/oncology
https://read.qxmd.com/read/21761578/ameloblastic-fibrosarcoma-a-cytologist-s-perspective
#54
JOURNAL ARTICLE
Nalini Gupta, Adarsh Barwad, Rajiv Kumar, Rijuneeta, Kim Vaiphei
Fine-needle aspiration cytology of a case of ameloblastic fibrosarcoma (AFS), an unusual odontogenic tumor related to ameloblastoma (AB), was performed in a 25-year-old female with a 1 cm swelling in the left lower orbital region along with involvement of zygomatic region. Aspiration of the tumor yielded a cellular sample composed predominantly of mesenchymal element and few clusters representing epithelial component showing tall columnar cells with peripheral palisading. Detailed cytomorphological features of AFS are discussed along with differential diagnosis from other tumors such as AB, desmoplastic AB, odontogenic fibroma, ameloblastic fibrodentinoma and ameloblastic fibro-odontoma, ameloblastic fibroma...
August 2011: Diagnostic Cytopathology
https://read.qxmd.com/read/21735142/a-previously-unreported-malignancy-of-the-thyroid
#55
JOURNAL ARTICLE
Bulent Cetin, Suleyman Buyukberber, Senem Senturk, Omer Uluoglu, Ugur Coskun, Mustafa Benekli
Ameloblastic fibrosarcoma or ameloblastic sarcoma is an extremely rare odontogenic neoplasm. We report a case of an ameloblastic fibrosarcoma arising from thyroid gland in a 44 year-old woman. Following total thyroidectomy, a histopathologic, immunohistologic, and genotypic examination revealed ameloblastic fibrosarcoma. The tumor was composed of odontogenic epithelium, resembling that of ameloblastoma, and a mesenchymal part exhibiting features of fibrosarcoma. To our review, our case represents the first report of ameloblastic fibrosarcoma of the thyroid gland...
September 2012: Medical Oncology
https://read.qxmd.com/read/21086277/differential-diagnosis-of-pediatric-tumors-of-the-nasal-cavity-and-paranasal-sinuses-a-45-year-multi-institutional-review
#56
MULTICENTER STUDY
F Christopher Holsinger, Adam C Hafemeister, M John Hicks, Marcelle Sulek, Winston W Huh, Ellen M Friedman
We conducted a retrospective case-series review to identify the various diagnoses of neoplasms of the nasal cavity and paranasal sinuses in a pediatric population. Our study group was made up of 54 children-23 boys and 31 girls, aged 8 months to 16 years (mean: 9 yr). All patients had been diagnosed with a tumor of the nasal cavity or paranasal sinuses between Jan. 1, 1955, and Dec. 31, 1999, at one of four university-based, tertiary care referral centers. We compiled data on tumoral characteristics (location, size, and histopathology), morbidity and mortality, and rates of recurrence...
November 2010: Ear, Nose, & Throat Journal
https://read.qxmd.com/read/21074695/immunoexpression-of-ki67-proliferative-cell-nuclear-antigen-and-bcl-2-proteins-in-a-case-of-ameloblastic-fibrosarcoma
#57
JOURNAL ARTICLE
Hélder Antônio Rebelo Pontes, Flávia Sirotheau Corrêa Pontes, Brunno Santos de Freitas Silva, Sérgio Elias Vieira Cury, Felipe Paiva Fonseca, Rodrigo Alves Salim, Décio dos Santos Pinto Júnior
Ameloblastic fibrosarcoma (AFS), regarded as the malignant counterpart of the benign ameloblastic fibroma, is an extremely rare odontogenic neoplasm with only 68 cases reported in the English literature up to 2009. It is composed of a benign odontogenic epithelium, resembling that of ameloblastoma, and a malignant mesenchymal part exhibiting features of fibrosarcoma. Due to the rarity of the lesion, little is known about its molecular pathogenesis; therefore, in the current study, we sought to evaluate the immunoexpression of Ki67, proliferative cell nuclear antigen, and Bcl-2 proteins in AFS, comparing the results obtained with its benign counterpart, as well as to report a new case of this rare entity affecting a 19-year-old female patient...
December 2010: Annals of Diagnostic Pathology
https://read.qxmd.com/read/19884826/ameloblastic-fibrosarcoma-involving-the-anterior-and-middle-skull-base-with-intradural-extension
#58
REVIEW
Bharat Guthikonda, Ehab Y Hanna, Roman J Skoracki, Sujit S Prabhu
Ameloblastic fibrosarcoma is a malignant odontogenic tumor that rarely affects the skull base and surrounding regions. We present a case of a 48-year-old man with histologically confirmed malignant transformation of a benign ameloblastic fibroma 10 years after initial presentation of a localized facial mass. The ameloblastic fibrosarcoma extended from the facial region to the orbit, anterior and middle fossa skull base, the infratemporal fossa, and the cavernous sinus. Progressive proptosis with complete monocular vision loss was the presenting symptom...
November 2009: Journal of Craniofacial Surgery
https://read.qxmd.com/read/19716496/rapid-sarcomatous-transformation-of-an-ameloblastic-fibroma-of-the-mandible-case-report-and-literature-review
#59
REVIEW
Aisha Kousar, Mervyn M Hosein, Zubair Ahmed, Khurram Minhas
Ameloblastic fibrosarcoma (AFS) is a rare malignant odontogenic tumour regarded as the malignant counterpart of ameloblastic fibroma. It is characterized by a benign epithelial component within a malignant fibrous stroma. AFS is a locally aggressive neoplasm with extremely low potential for metastasis. We report an extremely rare, rapidly progressive, and fatal case originating in the posterior mandible of a 20-year old female patient. Initially histopathologically diagnosed as a benign lesion, it rapidly recurred with apparent transformation into a high-grade sarcoma over a period of 6 months...
September 2009: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
https://read.qxmd.com/read/18392827/-malignant-odontogenic-tumors
#60
REVIEW
G Jundt, P A Reichart
Malignant odontogenic tumors are extremely rare. As with benign odontogenic tumors, malignant epithelial odontogenic tumors or odontogenic carcinomas are distinguished from the even rarer mesenchymal ones, the odontogenic sarcomas. The existence of odontogenic carcinosarcomas is not yet acknowledged by the World Health Organization. Odontogenic carcinomas comprise ameloblastic carcinoma (AmCa), primary intraosseous carcinoma (PIOC), clear cell odontogenic carcinoma, odontogenic ghost cell carcinoma (OGCC), and the special case of metastasizing ameloblastoma...
May 2008: Der Pathologe
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