• Title/Summary/Keyword: Odontogenic Tumor

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A CASE OF ODONTOGENIC MYXOMA RELATED TO BOTH IMPACTED CANINE TEETH IN THE MANDIBLE (소아에서 하악 양측 매복 견치와 연관된 치성 점액종)

  • Choi, Se-Hoon;Jeong, Jong-Cheol;Song, Min-Soek;Seo, Ji-Hoon;Kim, Soeng-Boem;Jun, Chang-Hun
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제29권1호
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    • pp.64-67
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    • 2003
  • Odontogenic myxoma is a rare tumor which occurs almost exclusively in the jaws, and seems to be of odontogenic origin. Clinically this tumor tends to appear in the second and third decades of life, and most of the lesions are located in the premolar - molar region. It is characterized grossly by mucoid or gelatinous gray-whitish tissue that replaces the cancellous bone and expands the cortex. It is invasive locally and has a high recurrence rate ranging from 10% to 33%. Radiographically, the appearance of this tumor is varied, but usually appears as a unilocular or multilocualr radioluscency of varying size. We experienced a rare case of odontogenic myxoma 12 years old patient related to mandibular bilateral impacted canines in the mandible, so we report this case with literature.

Cases report of ossifying fibroma showing various radiographic appearances in posterior mandible (하악골 후방부위에서 다양한 방사선학적 소견을 보이는 골화성섬유종의 증례보고)

  • Lee, Byung-Do;Oh, Seung-Hwan;Son, Hyun-Jin
    • Imaging Science in Dentistry
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    • 제40권1호
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    • pp.53-58
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    • 2010
  • Common radiographic appearances of ossifying fibroma (OF) are well demarcated margin, radiolucent or mixed lesion. Lesions for the radiographic differential diagnosis with OF include fibrous dysplasia, focal cemento-osseous dysplasia. Other confusing lesions might be the mixed lesions such as calcifying odontogenic cyst, adenomatoid odontogenic tumor, calcifying epithelial odontogenic tumor, and benign cementoblastoma. We reported three cases of OF in posterior mandible. These cases showed a little distinguished radiographic features of OF and diagnosed from a combination of clinical, radiographic, and histopathologic information. We need to further refine radiographic and histopathological features of OF and other confusing lesions with literatures review because some cases of these lesions are not easily differentiated radiographically and histopathologically.

Ameloblastic fibro-odontoma of the mandible (하악에 발생된 법랑모세포섬유치아종)

  • Kang Hyung-Wuk;Hwang Eui-Hwan;Lee Sang-Rae
    • Imaging Science in Dentistry
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    • 제33권1호
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    • pp.59-62
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    • 2003
  • Ameloblastic fibro-odontoma is an extremely rare odontogenic tumor composed of proliferating ectodermal and mesenchymal components of odontogenic tissue, containing hard tooth structure. It occurs predominantly in children and young adults. The mandibular molar-ramus area is the most frequently observed location, presenting radiographically as a well-circumscribed and radiolucent-radiopaque tumor. A case involving a 24-year-old woman presenting with a large ameloblastic fibro-odontoma of the posterior mandible is reported. This case is of radiologic interest because two distinct calcification patterns were observed.

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Recurrent odontogenic fibroma in a Formosan rock macaque (Macaca cyclopis)

  • Yeonsu Oh;Jongwoog Choi;Ho-Seong Cho
    • Korean Journal of Veterinary Service
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    • 제47권1호
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    • pp.49-53
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    • 2024
  • The animal in this case report was a 10-year-old male Taiwanese monkey (Macaca cyclopis) kept at a zoo of South Korea. Over the last three years, a cauliflower-shaped masses have been noted on the gingiva near the incisor and molar teeth on right maxilla. Consequently, this monkey have undergone surgical removal of the mass annually. Grossly masses showed pinkish color. Histopathological findings, typical spindle cell tumor composed of collagen fibers. Infiltration by plasma cells and lymphocytes is found unrelated to ulceration of the surface epithelium. This is the first report of peripheral odontogenic fibroma in a Formosan rock macaque.

Calcifying epithelial odontogenic tumor associated with the left mandibular first premolar: a case report and literature review

  • Kim, Won-Ki;Kim, Min-Soo;Lee, Eui-Mook;Cha, Jae-Won;Choi, Bo-Young;Kim, Bong-Chul;Min, Seung-Ki;Lee, Jun
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제38권3호
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    • pp.166-170
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    • 2012
  • Calcifying epithelial odontogenic tumor (CEOT) is a rarely reported benign tumor, accounting for 0.4-3% of all odontogenic tumors. Approximately 150 cases have been reported in the literature between 1958 and 2003. The age range of CEOT varies from 8 to 92 years with mean of 36.9 years, and the occurrence of the lesion in both genders is almost equal. It has 2 clinico-topographic variants: the intraosseous (94%) and the extraosseous (6%) type. The intraosseous type has a predilection for mandible (maxilla : mandible ratio of 1 : 2). The intraosseous CEOT commonly associated with non-erupted teeth accounts for more than half (52%) of the cases and usually appears as painless swelling that causes bony expansion. The location of diffused round-shaped calcifying material is inside the connective tissue stroma and epithelial islands. The tumors tend to be located toward the tooth crown, which usually has a unilocular radiolucent region containing variant radiopaque materials radiologically. In this paper, we report a case of CEOT occurring in the left mandibular first premolar of a 23-year-old female and present a brief review of the literature.

Peripheral odontogenic myxoma in a 12-year-old girl: a rare entity

  • Kanitkar, Sampada;Kamat, Mamata;Tamagond, Sridevi;Varekar, Aniruddha;Datar, Uma
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제43권3호
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    • pp.178-181
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    • 2017
  • Peripheral odontogenic myxoma is a rare odontogenic tumor representing an extra osseous counterpart of central odontogenic myxoma. It is commonly seen in gingiva between the 3rd and 4th decades of life and appears predominantly in females. Compared to central odontogenic myxoma, it is a less aggressive, slow-growing lesion with a low recurrence rate. However, close postoperative follow-up is required because of the unlimited growth potential of incompletely removed lesions. It shares many features with other soft tissue myxoid proliferations occurring in the oral cavity and hence needs to be differentiated from them. Very few cases of peripheral odontogenic myxomas have been reported and, to the best of our knowledge, no case has been reported in a pediatric patient. We present an unusual case of peripheral odontogenic myxoma occurring in a 12-year-old girl located in the anterior mandibular gingiva, with an emphasis on differential diagnosis.

Clinical study of keratocystic odontogenic tumors

  • Tomomatsu, Nobuyoshi;Uzawa, Narikazu;Michi, Yasuyuki;Kurohara, Kazuto;Okada, Norihiko;Amagasa, Teruo
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제38권1호
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    • pp.55-63
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    • 2012
  • The odontogenic keratocyst (OKC) was originally classified as a developmental cyst, and OKCs were histologically divided into orthokeratotic (O-OKCs) and parakeratotic (P-OKCs) types. Clinical features differ between O-OKCs and P-OKCs with P-OKCs having a tendency to recur after surgical treatment. According to the revised histopathological classification of odontogenic tumors by the World Health Organization (2005), the term keratocystic odontogenic tumor (KCOT) has been adopted to describe P-OKCs. In this retrospective study, we examined 186 KCOTs treated at the Maxillofacial Surgery Department of the Tokyo Medical and Dental University Hospital from 1981 through 2005. The patients ranged in age from 7 to 85 years (mean, 32.7) and consisted of 93 males and 93 females. The most frequently treated areas were the mandibular molar region and ramus. The majority of KCOTs in the maxillary region were treated by enucleation and primary closure. The majority of KCOTs in the mandibular region were enucleated, and the wound was left open. Marginal resection was performed in the 4 patients with large lesions arising in the mandible. In patients who were followed for more than a year, recurrences were observed in 19 of 120 lesions (15.8%). The recurrences were found at the margins of the primary lesion in contact with the roots of the teeth or at the upper margins of the mandibular ramus. Clinicians should consider aggressive treatment for KCOTs because the recurrence rate of P-OKCs is higher than that of other cyst types such as O-OKCs, dentigerous cysts, primordial cysts that were non-keratinized, and slightly keratinized stratified squamous epithelium. Although more aggressive treatment is needed for KCOTs as compared to other cystic lesions, it is difficult to make a precise diagnosis preoperatively on the basis of clinical features and X-ray imaging. Therefore, preoperative biopsy is necessary for selecting the appropriate treatment for patients with cystic lesions.

ODONTOGENIC FIBROMYXOMA;A CASE REPORT (치성섬유점액종;증례보고)

  • Kim, Su-Gwan;Kim, Woon-Kyu;Jang, Hyun-Seon
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제22권4호
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    • pp.464-468
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    • 2000
  • Odontogenic fibromyxomas are extremely rare benign odontogenic tumors that probably arise from interstitial portion of jaw bone. The plain X-ray showed osteolytic destructive lesions in the molar root area. CT scans demonstrated osteolytic expansile lesions with mild enhancement of the solid portion of the mass. Histologically, the tumor is composed of fibrous tissue and myxoid tissues. In this paper a case of odontogenic fibromyxoma of the maxilla and a review of the literature is presented.

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Diagnostic considerations in central odontogenic fibroma of the maxilla: 2 case reports

  • Seo, Yu-Kyeong;Kang, Ju Hee;Lee, Sae Rom;Choi, Yong-Suk;Hwang, Eui-Hwan;Oh, Song Hee
    • Imaging Science in Dentistry
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    • 제49권3호
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    • pp.229-234
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    • 2019
  • Central odontogenic fibroma (COF) is defined as a fibroblastic odontogenic tumor characterized by varying density of the tooth epithelium. It is an extremely rare benign neoplasm that occurs in the maxilla and the mandible; only a few reports of COF are available in the literature. Diagnosis of the lesion based only on the radiological features of COF is difficult due to variation in the findings regarding this condition. This report describes 2 clinical cases of middle-aged women with COF. Clinical examination revealed palatal mucosal depression; additionally, oral examination, as well as panoramic radiographs, intraoral radiographs, and computed tomography scans, revealed severe root resorption. This report highlights the clinical and radiological imaging features of COF, with the goal of enabling straightforward differential diagnosis of the lesion by the clinician and thereby appropriate treatment of the patient.

GLANDULAR ODONTOGENIC CYST : REPORT OF THREE CASES (선양치성낭 (Glandular odontogenic cyst) 3예)

  • Oh, Min-Sung;Yoon, Jung-Hoon;Kim, Hyung-Jun;Cha, In-Ho
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제27권2호
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    • pp.174-177
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    • 2001
  • Glandular odontogenic cyst(GOC) is a rare cyst of odontogenic origin, first described in 1988 by Gardner et al. Three glandular odontogenic cysts are presented which were experienced in the Dept. of Oral and Maxillofacial surgery, Yonsei University. The clinical characteristics, radiologic and histopathologic features, and method of treatment are discussed. One occured in the anterior maxilla, others in the mandible body area. One in the anterior maxilla showed swelling and tenderness, others not. All the lesion presented radiographically unilocular radiolucent lesion. Histopathologically, those were lined by nonkeratinizing stratified squamous epithelium of varying thickness showing plaque-like or spherical thickening. Partially, eosinophilic cuboidal cells lined the intraepithelial microcysts. Also, ciliated cuboidal cells and mucinous cells were observed. The cysts were treated by enucleation.

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