THE RADIOLOGY of ODONTOGENIC TUMORS Aug
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Benign Cementoblastoma Associated with an Impacted Mandibular Third Molar – Report of an Unusual Case
Case Report Benign Cementoblastoma Associated with an Impacted Mandibular Third Molar – Report of an Unusual Case Chethana Dinakar1, Vikram Shetty2, Urvashi A. Shetty3, Pushparaja Shetty4, Madhvika Patidar5,* 1,3Senior Lecturer, 4Professor & HOD, Department of Oral Pathology and Microbiology, AB Shetty Memorial Institute of Dental Science, Mangaloge, 2Director & HOD, Nittee Meenakshi Institute of Craniofacial Surgery, Mangalore, 5Senior Lecturer, Department of Oral Pathology and Microbiology, Babu Banarasi Das College of Dental Sciences, Lucknow *Corresponding Author: Email: [email protected] ABSTRACT Cementoblastoma is characterized by the formation of cementum-like tissue in direct connection with the root of a tooth. It is a rare lesion constituting less than 1% of all odontogenic tumors. We report a unique case of a large cementoblastoma attached to the lateral root surface of an impacted permanent mandibular third molar in a 33 year old male patient. The association of cementoblastomas with impacted teeth is a rare finding. Key Words: Odontogenic tumor, Cementoblastoma, Impacted teeth, Third molar, Cementum Access this article online opening limited to approximately 10mm. The swelling Quick Response was firm to hard in consistency and tender on palpation. Code: Website: Lymph nodes were not palpable. www.innovativepublication.com On radiographical examination, it showed a large, well circumscribed radiopaque mass attached to the lateral root surface of impacted permanent right mandibular DOI: 10.5958/2395-6194.2015.00005.3 third molar. The mass displayed a radiolucent area at the other end and was seen occupying almost the entire length of the ramus of mandible. The entire lesion was INTRODUCTION surrounded by a thin, uniform radiolucent line (Fig. -
Glossary for Narrative Writing
Periodontal Assessment and Treatment Planning Gingival description Color: o pink o erythematous o cyanotic o racial pigmentation o metallic pigmentation o uniformity Contour: o recession o clefts o enlarged papillae o cratered papillae o blunted papillae o highly rolled o bulbous o knife-edged o scalloped o stippled Consistency: o firm o edematous o hyperplastic o fibrotic Band of gingiva: o amount o quality o location o treatability Bleeding tendency: o sulcus base, lining o gingival margins Suppuration Sinus tract formation Pocket depths Pseudopockets Frena Pain Other pathology Dental Description Defective restorations: o overhangs o open contacts o poor contours Fractured cusps 1 ww.links2success.biz [email protected] 914-303-6464 Caries Deposits: o Type . plaque . calculus . stain . matera alba o Location . supragingival . subgingival o Severity . mild . moderate . severe Wear facets Percussion sensitivity Tooth vitality Attrition, erosion, abrasion Occlusal plane level Occlusion findings Furcations Mobility Fremitus Radiographic findings Film dates Crown:root ratio Amount of bone loss o horizontal; vertical o localized; generalized Root length and shape Overhangs Bulbous crowns Fenestrations Dehiscences Tooth resorption Retained root tips Impacted teeth Root proximities Tilted teeth Radiolucencies/opacities Etiologic factors Local: o plaque o calculus o overhangs 2 ww.links2success.biz [email protected] 914-303-6464 o orthodontic apparatus o open margins o open contacts o improper -
Misdiagnosis of Osteosarcoma As Cementoblastoma from an Atypical Mandibular Swelling: a Case Report
ONCOLOGY LETTERS 11: 3761-3765, 2016 Misdiagnosis of osteosarcoma as cementoblastoma from an atypical mandibular swelling: A case report ZAO FANG1*, SHUFANG JIN1*, CHENPING ZHANG1, LIZHEN WANG2 and YUE HE1 1Department of Oral Maxillofacial Head and Neck Oncology, Faculty of Oral and Maxillofacial Surgery; 2Department of Oral Pathology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai 200011, P.R. China Received December 1, 2014; Accepted January 12, 2016 DOI: 10.3892/ol.2016.4433 Abstract. Cementoblastoma is a form of benign odontogenic of the lesion with extraction of the associated tooth (2); tumor, with the preferred treatment consisting of tooth extrac- however, certain patients may decide against surgery, under- tion and follow-up examinations, while in certain cases, going follow-up alone. Osteosarcoma is a non-hematopoietic, follow-up examinations without surgery are performed. malignant tumor of the bone, with the neoplastic cells of the Osteosarcoma of the jaw is a rare, malignant, mesenchymal lesion producing osteoid (3). This form of tumor is character- tumor, associated with a high mortality rate and low incidence ized by high malignancy, metastasis and mortality rates (4). of metastasis. Cementoblastoma and osteosarcoma of the jaw The tumors are most prevalently located in the metaphyseal are dissimilar in terms of their histological type and prognosis; region of long bones, particularly in the knee and pelvis (5). however, there are a number of covert associations between Osteosarcoma of the jaw is rare, accounting for 5-13% of all them. The present study describes the case of a 20-year-old osteosarcoma cases (6), the majority of which are located in female with an unusual swelling in the left mandible that the mandible. -
Benign Cementoblastoma Associated with an Unerupted Third Molar - a Case Report
CORE Metadata, citation and similar papers at core.ac.uk Provided by Directory of Open Access Journals BENIGN CEMENTOBLASTOMA ASSOCIATED WITH AN UNERUPTED THIRD MOLAR - A CASE REPORT J.Dinakar* M.S.Senthil Kumar** Shiju Mathew Jacob*** *Professor & HOD, Department of Oral Pathology, ** Reader, *** Lecturer, Department of Oral Surgery, Sri Ramakrishna Dental College and Hospital, Coimbatore, Tamilnadu, India. ABSTRACT: Cementoblastoma is a rare odontogenic tumor derived from odontogenic ectomesenchyme of cementoblast origin that forms cementum layer on the roots of a tooth. A case report is presented of a patient treated with surgical excision of Cementoblastoma associated with an unerupted infected right lower third molar tooth. Key words: Cementoblastoma, Odontogenic tumour, unerupted third molar. The cell of origin is cementoblast. INTRODUCTION: Clinically it causes bony expansion. The commonest site is the posterior region of Cementoblastoma is an odontogenic the mandible. In the radiograph it is seen tumor of ectomesenchymal origin. It is as large radiopaque mass associated with also called cementoma. They are large the root of the tooth. We report a case of bulbous mass of cementum or cementum- Benign Cementoblastoma from Sri like tissue on roots of teeth. Ramakrishna Dental College & Hospital, Coimbatore. restriction in opening the mouth and intra oral examination reveals a partially CASE REPORT: erupted third molar tooth with pus discharge. A panoramic radiograph A 41 year old man presented to our showed a radio-opaque, dense, department with a complaint of pain and amorphous, irregularly shaped mass swelling in the right lower half of the face. measuring 2.2 x 1.5cm attached with the Patient gave history of intermittent pain third molar (Fig 1,1a). -
Ameloblastoma of the Maxillary Sinus 11 Years After Extirpation of Extensive Dentigerous Cysts and Dystopic Wisdom Tooth
in vivo 24: 567-570 (2010) Ameloblastoma of the Maxillary Sinus 11 Years after Extirpation of Extensive Dentigerous Cysts and Dystopic Wisdom Tooth REINHARD E. FRIEDRICH1 and JOZEF ZUSTIN2 1Oral and Maxillofacial Surgery, and 2Pathology, Eppendorf University Hospital, University of Hamburg, Germany Abstract. We present the case of a 36-year-old patient with bone is depicted on adequate radiographs. The tumor replaces ameloblastoma of the maxillary sinus. The history of the the bone by small, radiographically well-defined areas often patient was extraordinary with respect to the diagnosis of an resulting in a honey comb-like translucency (2). This feature is extensive odontogenic cyst of this sinus with a maxillary supported by the insufficient regeneration of bone that might wisdom tooth located far from the region of origin. Both cyst result in osseous expansion of the affected site (8). Association and tooth had been completely extirpated more than 10 years of ameloblastoma with dentigerous cysts is well-documented, prior to the current tumor diagnosis. Diagnosis of in particular the development of ameloblastoma in a ameloblastoma was based on routinely processed specimen and histologically proven cyst with the retained tooth inside the supported by immunohistochemical markers. Localization and bone, and in keratocystic odontogenic tumor (12-14). The extension of both cyst and neoplasm support the assumption amount of tumor inside a dentigerous cyst might vary that both entities arose from the same area. Long-term follow- considerably. On the other hand the association of dentigerous up is recommended in the treatment of odontogenic cysts. cysts with ameloblastomas was called into question (15). -
Odontogenic Keratocyst with Ameloblastomatous Dentistry Section Transformation: a Rare Case Report
Case Report DOI: 10.7860/JCDR/2020/43336.13636 Odontogenic Keratocyst with Ameloblastomatous Dentistry Section Transformation: A Rare Case Report METEHAN KESKIN1, NILÜFER ÖZKAN2, NIHAT AKBULUT3, MEHMET CIHAN BEREKET4 ABSTRACT Odontogenic Keratocysts (OKC) are a developmental odontogenic cysts arising from remnants of the dental lamina. They differ from other odontogenic cysts due to their aggressive growth behaviour and high recurrence rates. Malignant or benign transformation may develop from their epithelium. Ameloblastomatous transformation of OKC is an extremely rare case. Such lesions have been described as combined or hybrid odontogenic lesions. In this case report, a 22-year-old patient presented with an unusual lesion in the mandible showing histological features of both OKC and ameloblastoma, and review of the available literature regarding the combined lesions. Keywords: Combined lesion, Hybrid lesion, Marginal resection, Mandible CASE REPORT corrugated parakeratosis, approximately 4-6 cell layers and palisaded A systemically healthy 22-year-old male patient was referred to basal cell layer resembling the OKC [Table/Fig-2a]. Some areas Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, inside the cyst wall showed stellate reticulum-like epithelial cells and Ondokuz Mayıs University, Turkey with painless swelling in the a basal cell layer of tall columnar cells with palisaded, revers polarised left lower jaw for 2 months. Three weeks before the first visit, the nuclei resembling the ameloblastomatous epithelium [Table/Fig-2b]. patient was prescribed antibiotics by another dental clinic because The lesion was diagnosed as Odontogenic Keratocyst (OKC) with of swelling in the left side of the jaw. On extraoral examination, a ameloblastomatous transformation. -
Parotid Adenoid Cystic Carcinoma: a Case Report and Review of The
ancer C C as & e y Ilson et al., Oncol Cancer Case Rep 2015,1:1 g R o e l p o o c r t n Oncology and Cancer Case O ISSN: 2471-8556 Reports ResearchCase Report Article OpenOpen Access Access Parotid Adenoid Cystic Carcinoma: A Case Report and Review of the Literature Sepúlveda Ilson1*, Frelinghuysen Michael2, Platín Enrique3, Ortega Pablo4 and Delgado Carolina5 1Maxillofacial-Head and Neck Radiologist, ENT-Head and Neck Surgery Service, General Hospital of Concepcion, Chile 2Physician, Radiation Oncologist, Oncology Service, General Hospital of Concepcion, Chile 3Professor of Oral and Maxillofacial Radiology, University of North Carolina School of Dentistry, Chapel Hill, NC, USA 4Physician, Otolaryngologist, ENT-Head and Neck Surgery Service, General Hospital of Concepcion, Chile 5Physician Pathologist, Pathology Department, General Hospital of Concepción, University of Concepcion School of Medicine, Concepcion, Chile Abstract We report on a patient who presented to the ENT service with swelling of the right side of the parotid gland. The swelling had been present for four years. Imaging studies revealed an expansive process confined to the superficial right parotid lobule. The affected area was well delineated with irregular enhancement post intravenous contrast media administration. Surgical biopsy concluded the presence of Adenoid Cystic Carcinoma. The patient was treated with adjuvant radiation therapy and follow up exams confirm there is no evidence of recurrence. Introduction Adenoid cystic carcinoma (ACC) is malignant epithelial tumors that most commonly occur between the 5th and 6th decades of life. It is a slowly growing but highly invasive cancer with a high recurrence rate. This tumor has the propensity for perineural invasion. -
Maxillary Ameloblastoma: a Review with Clinical, Histological
in vivo 34 : 2249-2258 (2020) doi:10.21873/invivo.12035 Review Maxillary Ameloblastoma: A Review With Clinical, Histological and Prognostic Data of a Rare Tumor ZOI EVANGELOU 1, ATHINA ZARACHI 2, JEAN MARC DUMOLLARD 3, MICHEL PEOC’H 3, IOANNIS KOMNOS 2, IOANNIS KASTANIOUDAKIS 2 and GEORGIA KARPATHIOU 1,3 Departments of 1Pathology and Otorhinolaryngology, and 2Head and Neck Surgery, University Hospital of Ioannina, Ioannina, Greece; 3Department of Pathology, University Hospital of Saint-Etienne, Saint-Etienne, France Abstract. Diagnosis of odontogenic tumors can be neoplasms, diagnosis could be straightforward. In locations challenging due to their rarity and diverse morphology, but outside the oral cavity or when rare histological variants are when arising near the tooth, the diagnosis could be found, suspecting the correct diagnosis can be challenging. suspected. When their location is not typical, like inside the This is especially true for maxillary ameloblastomas, which paranasal sinuses, the diagnosis is less easy. Maxillary are rare, possibly leading to low awareness of this neoplasm ameloblastomas are exceedingly rare with only sparse at this location and often show non-classical morphology, information on their epidemiological, histological and genetic thus, rendering its diagnosis more complicated. characteristics. The aim of this report is to thoroughly review Thus, the aim of this review is to define and thoroughly the available literature in order to present the characteristics describe maxillary ameloblastomas based on the available of this tumor. According to available data, maxillary literature after a short introduction in the entity of ameloblastomas can occur in all ages but later than mandible ameloblastoma. ones, and everywhere within the maxillary region without necessarily having direct contact with the teeth. -
Odontogenic Tumors
4/26/20 CONTEMPORARY MANAGEMENT OF ODONTOGENIC TUMORS RUI FERNANDES, DMD, MD,FACS, FRCS(ED) PROFESSOR UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE- JACKSONVILLE 1 2 Benign th 4 Edition Odontogenic 2017 Tumors Malignant 3 4 BENIGN ODONTOGENIC TUMORS BENIGN ODONTOGENIC TUMORS • EPITHELIAL • MESENCHYMAL • AMELOBLASTOMA • ODONTOGENIC MYXOMA • CALCIFYING EPITHELIAL ODONTOGENIC TUMOR • ODONTOGENIC FIBROMA • PINDBORG TUMOR • PERIPHERAL ODONTOGENIC FIBROMA • ADENOMATOID ODONTOGENIC TUMOR • CEMENTOBLASTOMA • SQUAMOUS ODONTOGENIC TUMOR • ODONTOGENIC GHOST CELL TUMOR 5 6 1 4/26/20 BENIGN ODONTOGENIC TUMORS MALIGNANT ODONTOGENIC TUMORS • PRIMARY INTRAOSSEOUS CARCINOMA • MIXED TUMORS • CARCINOMA ARISING IN ODONTOGENIC CYSTS • AMELOBLASTIC FIBROMA / FIBRO-ODONTOMA • AMELOBLASTIC FIBROSARCOMA • ODONTOMA • AMELOBLASTIC SARCOMA • CLEAR CELL ODONTOGENIC CARCINOMA • ODONTOAMELOBLASTOMA • SCLEROSING ODONTOGENIC CARCINOMA New to the Classification • PRIMORDIAL ODONTOGENIC TUMOR New to the Classification • ODONTOGENIC CARCINOSARCOMA 7 8 0.5 Cases per 100,000/year Ameloblastomas 30%-35% Myxoma AOT 3%-4% Each Ameloblastic fibroma CEOT Ghost Cell Tumor 1% Each 9 10 Courtesy of Professor Ademola Olaitan AMELOBLASTOMA • 1% OF ALL CYSTS AND TUMORS • 30%-60% OF ALL ODONTOGENIC TUMORS • 3RD TO 4TH DECADES OF LIFE • NO GENDER PREDILECTION • MANDIBLE 80% • MAXILLA 20% 11 12 2 4/26/20 AMELOBLASTOMA CLASSIFICATION AMELOBLASTOMA HISTOLOGICAL CRITERIA • SOLID OR MULTI-CYSTIC Conventional 2017 • UNICYSTIC 1. PALISADING NUCLEI 2 • PERIPHERAL 2. REVERSE POLARITY 3. VACUOLIZATION OF THE CYTOPLASM 4. HYPERCHROMATISM OF BASAL CELL LAYER 1 3 4 AmeloblAstomA: DelineAtion of eArly histopathologic feAtures of neoplasiA Robert Vickers, Robert Gorlin, CAncer 26:699-710, 1970 13 14 AMELOBLASTOMA CLASSIFICATION OF 3677 CASES AMELOBLASTOMA SLOW GROWTH – RADIOLOGICAL EVIDENCE Unicystic Peripheral 6% 2% Solid 92% ~3 yeArs After enucleAtion of “dentigerous cyst” P.A . -
ODONTOGENIC TUMORS: WHERE ARE WE in 2017? Odontojen Tümörler
S10 J Istanbul Univ Fac Dent 2017;51(3 Suppl 1):S10-S30. http://dx.doi.org/10.17096/jiufd.52886 INVITED REVIEW ODONTOGENIC TUMORS: WHERE ARE WE IN 2017? Odontojen Tümörler: 2017 Yılında Neredeyiz? John M WRIGHT 1, Merva SOLUK-TEKKEŞIN 2 Received: 05/07/2017 Accepted:04/08/2017 ABSTRACT ÖZ Odontogenic tumors are a heterogeneous group of Odontojen tümörler, klinik davranışlarına ve lesions of diverse clinical behavior and histopathologic histopatolojik özelliklerine göre hamartomdan maligniteye types, ranging from hamartomatous lesions to malignancy. kadar değişen heterojen bir grup lezyondur. Bu tümörler, Because odontogenic tumors arise from the tissues which dişleri oluşturan dokulardan köken aldığı için çenelere make our teeth, they are unique to the jaws, and by extension özgüdür ve genellikle diş hekimliğini ilgilendirir. Odontojen almost unique to dentistry. Odontogenic tumors, as in normal tümörler normal odontogenezis sürecinde olduğu gibi odontogenesis, are capable of inductive interactions between odontojen ektomezenkim ve epitel arasındaki karşılıklı odontogenic ectomesenchyme and epithelium, and the indüksiyon mekanizmasıyla ortaya çıkar ve bu tümörlerin classification of odontogenic tumors is essentially based sınıflamasında bu indüksiyon mekanizması baz alınır. on this interaction. The last update of these tumors was Odontojen tümörlerle ilgili en son güncelleme 2017 published in early 2017. According to this classification, yılının başında yapılmıştır. Bu sınıflamaya göre; iyi huylu benign odontogenic tumors are classified -
Ameloblastic Fibroma: a Case Report
Oral Pathology in linical and Laboratorial 251 Research in Dentistry Ameloblastic fibroma: a case report • Eloisa Muller de Carvalho Department of Radiology, School of Dentistry, São Paulo University, São Paulo, Brazil • Fernando Kendi Horikawa Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil • Leticia Guimaraes Department of Oral Pathology, School of Dentistry, University of São Paulo, São Paulo, Brazil • Stephanie Kenig Viveiros Department of Oral Pathology, School of Dentistry, University of São Paulo, São Paulo, Brazil • Celso Augusto Lemos Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, Brazil • Juliane Piragine Araujo Department of Radiology, School of Dentistry, University of São Paulo, São Paulo, Brazil ABSTRACT | Ameloblastic fibroma is a rare benign odontogenic tumor in which both epithelial and ectomesenchymal components are neoplastic. A 24-year-old male patient was referred to the Stomatology Department with difficulty to chew and swelling in the right posterior region of the mandible. The panoramic radiograph showed a well-circumscribed, uni- locular radiolucent lesion with partially radiopaque borders involving first and second unerupted molars. Computed tomography imaging presented a hypodense image with well-delimited isodense content, bulging and rupture of corti- cal bones. The patient underwent an incisional biopsy. Microscopically, the lesion was composed of many mesenchymal tissue cells in strand form, arranged in cords, islands and nests of odontogenic epithelium; the diagnostic was amelo- blastic fibroma. The patient was referred to the hospital for enucleation and curettage of the lesion and extraction of the associated teeth. After 8 months of follow-up, no recurrence was observed. -
An Extrafollicular Adenomatoid Odontogenic Tumor Mimicking a Periapical Cyst
Hindawi Case Reports in Radiology Volume 2018, Article ID 6987050, 5 pages https://doi.org/10.1155/2018/6987050 Case Report An Extrafollicular Adenomatoid Odontogenic Tumor Mimicking a Periapical Cyst Farzaneh Mosavat ,1 Roxana Rashtchian,1 Negar Zeini ,1 Daryoush Goodarzi Pour,1 Shabnam Mohammed Charlie,1 and Nazanin Mahdavi2 1 Oral and Maxillofacial Radiology Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran 2Oral and Maxillofacial Pathology Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran Correspondence should be addressed to Negar Zeini; [email protected] Received 4 April 2017; Accepted 13 July 2017; Published 1 January 2018 Academic Editor: Soon Tye Lim Copyright © 2018 Farzaneh Mosavat et al. Tis is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Adenomatoid odontogenic tumor (AOT) is a rare noninvasive odontogenic tumor that occurs mostly in the second decade of life. Based on its tooth association, AOT can be classifed into three categories of follicular, extrafollicular, and peripheral types; the follicular classifcation is considered as the most common type of AOT. Tis study reported a large extrafollicular case of AOT in a 40-year-old female. She was asymptomatic and tumor was detected accidentally by her dental practitioner. Since the panoramic radiograph showed a well-defned unilocular radiolucent lesion, we observed radiopaque spots within the lesion by using cone beam computed tomography. Te extrafollicular type can mimic a periapical radiolucent lesion. 1. Introduction attached to the gingival structures [9].