This document discusses three odontogenic tumors: adenomatoid odontogenic tumor, calcifying epithelial odontogenic tumor, and odontogenic myxoma. It provides information on the classification, histopathological features, clinical presentation, diagnosis and treatment of each tumor type. The key points are that adenomatoid odontogenic tumor commonly occurs in younger patients, presents as a radiolucent lesion associated with an unerupted tooth, and has a benign clinical course. Calcifying epithelial odontogenic tumor is characterized by islands of epithelial cells surrounded by amyloid-like calcified material. Odontogenic myxoma presents as an expansile radiolucent lesion containing myxoid tissue.
- Adenomatoid odontogenic tumor (AOT) is a rare, benign tumor that occurs mostly in the maxilla near unerupted teeth.
- It affects females more than males on average around 18 years of age. Radiographically, it appears as a well-defined radiolucency that may have faint radiopacities from calcification.
- Microscopically, AOT contains duct-like structures lined with epithelial cells and surrounded by stellate reticulum-like cells. Treatment involves conservative surgical excision due to its slow-growing but progressive nature.
The document provides information about Pindborg tumor, also known as calcifying epithelial odontogenic tumor (CEOT). It defines CEOT as a locally invasive epithelial odontogenic neoplasm characterized by the presence of amyloid material that may become calcified. The document discusses the pathogenesis, histopathological features including epithelial cells, amyloid-like material and calcific deposits, immunohistochemical findings, differential diagnosis and treatment of CEOT. It also mentions the recurrence rate of CEOT is typically 10-15% but can be higher in certain variants.
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Benign, locally aggressive tumor of odontogenic epithelium, Previously called adamantinoma, Second most common odontogenic tumor after odontoma, Mandible is most common site, Usually asymptomatic and can be found incidentally on routine dental examinations
Peripheral and central giant cell granulomaRijuwana77
This document discusses two types of non-epithelial tumours of the oral cavity: peripheral giant cell granuloma and central giant cell granuloma. Peripheral giant cell granuloma originates from the periodontal membrane or alveolar bone and presents as a soft tissue nodule composed of multinucleated giant cells. Central giant cell granuloma is a rare, benign, intraosseous lesion most commonly found in the mandible of young people that causes expansion of the bone and resorption of tooth roots. Both lesions contain proliferation of multinucleated giant cells and other cells and may require surgical excision, with central giant cell granuloma having a higher rate of recurrence.
This document provides information about calcifying odontogenic cysts (COCs). It defines COCs and classifies them according to the WHO. COCs are rare jaw lesions characterized by ghost cells and calcifications. They are thought to arise from odontogenic epithelial remnants. Clinically, they typically present in the second decade of life with lesions more common in the maxilla than mandible. Radiographically, COCs appear well-defined with variable calcifications. Histologically, they contain ghost cells and basal cell layer with hyperchromatic nuclei. Prognosis is generally good when treated with surgical removal.
This document discusses several pathologies that can affect the jaws, including:
1. The adenomatoid odontogenic tumor, which presents as a swelling in young patients around unerupted teeth and consists of epithelial cells and calcifications.
2. The calcifying epithelial odontogenic tumor, which occurs in the mandible or maxilla as a radiolucent lesion containing radiopacities from calcification.
3. Odontomas, which are hamartomas containing dental tissues like enamel and dentin that appear as radiopaque masses and require conservative excision.
This document discusses and compares different types of non-odontogenic (not related to teeth) cysts. It separates them into developmental and inflammatory cysts. Developmental cysts form due to epithelial cell remnants becoming trapped during embryonic development, while inflammatory cysts form due to duct obstruction or trauma. Some examples of developmental cysts mentioned are nasopalatine duct cysts, median palatal cysts, and dermoid cysts. Inflammatory cysts include mucoceles, ranulas caused by salivary gland duct obstruction, and retention cysts of the maxillary sinus. The document provides details on pathogenesis, clinical features, histopathology, diagnosis and treatment of several of these cyst types.
- Adenomatoid odontogenic tumor (AOT) is a rare, benign tumor that occurs mostly in the maxilla near unerupted teeth.
- It affects females more than males on average around 18 years of age. Radiographically, it appears as a well-defined radiolucency that may have faint radiopacities from calcification.
- Microscopically, AOT contains duct-like structures lined with epithelial cells and surrounded by stellate reticulum-like cells. Treatment involves conservative surgical excision due to its slow-growing but progressive nature.
The document provides information about Pindborg tumor, also known as calcifying epithelial odontogenic tumor (CEOT). It defines CEOT as a locally invasive epithelial odontogenic neoplasm characterized by the presence of amyloid material that may become calcified. The document discusses the pathogenesis, histopathological features including epithelial cells, amyloid-like material and calcific deposits, immunohistochemical findings, differential diagnosis and treatment of CEOT. It also mentions the recurrence rate of CEOT is typically 10-15% but can be higher in certain variants.
Odontogenic keratocyst (OKC) is the cyst arising from the cell rests of dental lamina. It can occur anywhere in the jaw, but commonly seen in the posterior part of the mandible. Radiographically, most OKCs are unilocular when presented at the periapex and can be mistaken for radicular or lateral periodontal cyst.
Benign, locally aggressive tumor of odontogenic epithelium, Previously called adamantinoma, Second most common odontogenic tumor after odontoma, Mandible is most common site, Usually asymptomatic and can be found incidentally on routine dental examinations
Peripheral and central giant cell granulomaRijuwana77
This document discusses two types of non-epithelial tumours of the oral cavity: peripheral giant cell granuloma and central giant cell granuloma. Peripheral giant cell granuloma originates from the periodontal membrane or alveolar bone and presents as a soft tissue nodule composed of multinucleated giant cells. Central giant cell granuloma is a rare, benign, intraosseous lesion most commonly found in the mandible of young people that causes expansion of the bone and resorption of tooth roots. Both lesions contain proliferation of multinucleated giant cells and other cells and may require surgical excision, with central giant cell granuloma having a higher rate of recurrence.
This document provides information about calcifying odontogenic cysts (COCs). It defines COCs and classifies them according to the WHO. COCs are rare jaw lesions characterized by ghost cells and calcifications. They are thought to arise from odontogenic epithelial remnants. Clinically, they typically present in the second decade of life with lesions more common in the maxilla than mandible. Radiographically, COCs appear well-defined with variable calcifications. Histologically, they contain ghost cells and basal cell layer with hyperchromatic nuclei. Prognosis is generally good when treated with surgical removal.
This document discusses several pathologies that can affect the jaws, including:
1. The adenomatoid odontogenic tumor, which presents as a swelling in young patients around unerupted teeth and consists of epithelial cells and calcifications.
2. The calcifying epithelial odontogenic tumor, which occurs in the mandible or maxilla as a radiolucent lesion containing radiopacities from calcification.
3. Odontomas, which are hamartomas containing dental tissues like enamel and dentin that appear as radiopaque masses and require conservative excision.
This document discusses and compares different types of non-odontogenic (not related to teeth) cysts. It separates them into developmental and inflammatory cysts. Developmental cysts form due to epithelial cell remnants becoming trapped during embryonic development, while inflammatory cysts form due to duct obstruction or trauma. Some examples of developmental cysts mentioned are nasopalatine duct cysts, median palatal cysts, and dermoid cysts. Inflammatory cysts include mucoceles, ranulas caused by salivary gland duct obstruction, and retention cysts of the maxillary sinus. The document provides details on pathogenesis, clinical features, histopathology, diagnosis and treatment of several of these cyst types.
This document discusses odontomas, which are benign odontogenic tumors composed of dental tissue like enamel, dentin, and pulp. There are two main types: compound odontomas, which appear like small tooth structures, and complex odontomas, which have a disorganized appearance. Odontomas are usually asymptomatic and discovered incidentally on x-rays during dental exams. On x-rays, they appear as radiopaque masses surrounded by a radiolucent rim. Treatment involves simple surgical removal, with an excellent prognosis and no recurrence.
The document discusses several types of odontogenic tumors that can occur in the jaws. It focuses on describing ameloblastoma, adenomatoid tumor, and calcifying epithelial odontogenic tumor. Ameloblastoma is a benign but locally aggressive tumor arising from odontogenic epithelium. It commonly presents as a painless swelling in the mandible and radiographs show multilocular radiolucency. Histologically there are follicular or plexiform patterns. Adenomatoid tumor is a rare benign tumor associated with impacted teeth. Calcifying epithelial odontogenic tumor is a rare, locally aggressive tumor that can be mistaken for carcinoma, presenting with calcified masses visible on radiographs.
This document discusses odontogenic keratocysts (OKCs), a type of jaw cyst. It covers the classification, causes, histopathology, clinical features, radiographic features, differential diagnosis, treatment principles, and surgical treatment options for OKCs. OKCs most commonly occur in the mandibular molar and ramus areas and are often radiolucent and multilocular in appearance on radiographs. Treatment options include wide surgical excision or marsupialization to prevent recurrence of these cysts which have a high rate of recurrence compared to other jaw cysts.
This document discusses red and white lesions of the oral cavity, focusing on oral candidiasis. It describes the various types of oral candidiasis including pseudomembranous, erythematous, chronic plaque-type, and median rhomboid glossitis. Predisposing factors, clinical findings, diagnosis, treatment with antifungal medications or surgery, and prognosis are summarized for each type. Chronic hyperplastic candidiasis may require long-term antifungal therapy or surgery due to risk of recurrence. Overall prognosis is generally good if predisposing factors can be addressed.
The document discusses the classification of odontogenic cysts. It describes several classification systems proposed over time, including Robinson's classification from 1945, Thoma-Robinson-Bernier classification from 1960, Pindborg and Kramer's classification from 1971, and the WHO classification from 1971 and its update in 1992. The WHO classifications categorize cysts as developmental or inflammatory, and further divide developmental cysts into odontogenic and non-odontogenic types. Shafer's classification also categorizes cysts based on etiology as developmental or inflammatory, and further divides them based on the tissue of origin.
This document discusses radicular cysts, which are the most common inflammatory cysts in the oral cavity. Radicular cysts arise from epithelial residues in the periodontal ligament as a result of periapical periodontitis following pulp necrosis. They are usually asymptomatic but can cause swelling and bone resorption as they expand. The cyst forms from the proliferation of epithelial cell rests in the granulation tissue surrounding the apex of an infected tooth. Histologically, they are lined by stratified squamous epithelium and surrounded by fibrous connective tissue that may contain cholesterol crystals. Treatment involves root canal therapy or extraction with curettage of the cyst lining.
This document discusses fibro-osseous lesions, which replace normal bone with fibrous tissue containing newly formed mineralized structures. It describes several types of fibro-osseous lesions including fibrous dysplasia, cemento-osseous dysplasias like periapical cemental dysplasia, and fibro-osseous neoplasms like ossifying fibroma. For each type, it covers definitions, clinical features, radiographic appearances, differential diagnosis, and treatment approaches.
Calcifying epithelial odontogenic tumor is a rare, aggressive but benign odontogenic tumor accounting for 1% of all odontogenic tumors. It was first recognized by Pindborg and is of epithelial origin. Intraosseous tumors are more common than extraosseous tumors. Radiographically, it appears as a radiolucency that may contain small radiopacities. Surgical removal by enucleation is the treatment of choice, with recurrence rates of 10-15%.
The document discusses different types of cysts that can occur in the oral and maxillofacial region. It defines cysts and classifies them based on their origin and location. It provides details on the pathogenesis, clinical features, radiographic appearance and histology of specific cysts such as dentigerous cysts and odontogenic keratocysts. Dentigerous cysts are defined as cysts originating from the separation of the dental follicle from around the crown of an unerupted tooth. Odontogenic keratocysts are distinctive cysts that arise from cell rests of the dental lamina and have more aggressive behavior than other cysts. Complications of cysts include recurrence, development of
Radicular cysts originate from epithelial cell rests of Malassez and form through three phases: initiation, cyst formation, and growth/enlargement. They are usually painless unless infected and associated with nonvital teeth. Calcifying odontogenic cysts contain ghost cells, which represent abnormal keratinization and have an affinity for calcification. They may also induce dental tissue formation. Keratocystic odontogenic tumors initiate from dental lamina proliferation and enlarge through factors like osmolality, inflammatory exudate, glycosaminoglycans, and collagenolytic/bone resorbing molecules. Their thin fragile linings and intrinsic growth potential contribute to high recurrence rates.
Oral lichen planus is a chronic inflammatory disease that affects the oral mucosa. It is characterized by white striations (Wickham's striae) and varies in appearance from reticular to erythematous or ulcerative lesions. The cause is unknown but involves a cell-mediated immune response. Treatment focuses on reducing symptoms and includes topical corticosteroids, immunosuppressants, or retinoids. Malignant transformation may rarely occur so follow-up is important.
This document discusses mixed odontogenic tumors and odontogenic sarcomas according to the 2005 WHO classification. It provides details on ameloblastic fibroma, its clinical features, histopathology, radiographic features and differential diagnosis. It also discusses ameloblastic fibro-odontoma and fibro-dentinoma, calcifying cystic odontogenic tumor, complex and compound odontomas, and odontoameloblastoma. The key information provided includes the definitions, epidemiology, clinical and radiographic presentation, histopathology, and differential diagnosis of these odontogenic lesions.
This document discusses various mucocutaneous disorders of the oral cavity, including genodermatoses, infective causes, and non-infective conditions. It provides details on specific diseases such as erythema multiforme, pemphigus, and cicatricial pemphigoid. Erythema multiforme is characterized by target lesions that can involve the oral mucosa. Pemphigus is a chronic blistering disease caused by loss of cell adhesion, while cicatricial pemphigoid involves subepithelial blistering that results in scarring.
This document discusses various types of pseudocysts and true cysts found in the body. It begins by defining the key differences between a true cyst and a pseudocyst. Pseudocysts are lined by granulation and/or fibrous tissue rather than an epithelial cell layer. The document then classifies and describes different types of pseudocysts including traumatic bone cysts, aneurysmal bone cysts, and developmental cysts. It provides details on the etiology, location, patient demographics, clinical presentation, radiographic features, histopathology and treatment for each type.
This document describes a case report of a peripheral ossifying fibroma (POF) in a 22-year-old female patient. POFs are non-neoplastic reactive lesions of the gingiva caused by local irritants like plaque or food impaction. Histopathological examination showed fibrous connective tissue with bony trabeculae and dystrophic calcification, consistent with POF. Treatment involves complete surgical excision to remove the lesion and any remaining irritants in order to reduce the risk of recurrence.
This document discusses classifications and clinical relevance of oral epithelial dysplasia in assessing risk of oral potentially malignant disorders. It describes various classification systems for grading dysplasia including WHO and Ljubljana systems. Key histopathological features of dysplasia are loss of maturation and increased nuclear-cytoplasmic ratio. Higher risk of malignant transformation is seen with factors like female gender, long standing lesions, location on tongue/floor of mouth, large size and presence of dysplasia. Accurate grading helps determine prognosis and clinical management.
The document discusses various periodontal instruments used in dental procedures like probing, scaling, root planing, and surgery. It describes the purpose and usage of different types of probes, scalers, curettes, ultrasonic instruments and other tools. Key details about Gracey curettes, sickle scalers, hoe scalers and techniques like adaptation, angulation and strokes are provided.
Regional odontodysplasia is a developmental anomaly affecting the ectodermal and mesodermal components of tooth development, causing teeth to be small, mottled brown, and hypocalcified. It most commonly impacts the central and lateral incisors. Radiographically, affected teeth appear ghost-like with reduced density and large pulp chambers. While the etiology is uncertain, factors like trauma, infection, and vascular defects have been suggested. Clinical diagnosis is based on irregular tooth shape and brown discoloration, while radiographs reveal a shell-like appearance. Treatment typically involves early extraction and prosthetic replacement, though restorative procedures like root canals may attempt to save affected teeth.
This document provides information on vesiculobulllous lesions, including their classification, pathophysiology, diagnosis, types of pemphigus, clinical features, pathogenesis, histopathology, confirmatory diagnosis, differential diagnosis, and treatment. It discusses conditions like pemphigus vulgaris, pemphigoid, paraneoplastic pemphigus. Pemphigus vulgaris involves autoantibodies against desmogleins 1 and 3, causing blistering in skin and mucosa. Paraneoplastic pemphigus is associated with neoplasms and involves multiple organs. Diagnosis involves biopsy, DIF, and ELISA to detect specific autoantibodies.
The document summarizes information about periapical cysts, also known as radicular cysts or apical cysts. It defines a periapical cyst as an odontogenic cyst derived from cell rests of Malassez that proliferate in response to inflammation from pulpal necrosis. Periapical cysts typically present as round radiolucencies associated with the apex of a non-vital tooth. Histologically, they contain a lumen lined by stratified squamous epithelium and surrounded by a fibrous connective tissue wall. Treatment involves extraction of the involved tooth along with cyst enucleation or marsupialization.
This document provides an overview of odontogenic tumors, including their classification and descriptions of common tumors. It discusses key features of ameloblastoma, including clinical presentation, radiographic appearance and histopathological variants. Unicystic and peripheral ameloblastomas are also described. Other tumors covered include adenomatoid odontogenic tumor, calcifying epithelial odontogenic tumor, and compound and complex odontomas. For each tumor, the summary highlights critical information on classification, clinical features, radiology, histopathology and differential diagnosis.
This document discusses different types of odontogenic tumors. It classifies them into three categories: tumors of odontogenic epithelium, mixed odontogenic tumors, and tumors of odontogenic ectomesenchyme. Key tumors discussed include ameloblastoma, adenomatoid odontogenic tumor (AOT), and calcifying epithelial odontogenic tumor (CEOT). Ameloblastoma is the most common odontogenic tumor and can be solid/multicystic, unicystic, or peripheral. AOT typically occurs in younger females in the anterior maxilla. CEOT accounts for less than 1% of odontogenic tumors and resembles cells of the enamel organ or dental lamina.
This document discusses odontomas, which are benign odontogenic tumors composed of dental tissue like enamel, dentin, and pulp. There are two main types: compound odontomas, which appear like small tooth structures, and complex odontomas, which have a disorganized appearance. Odontomas are usually asymptomatic and discovered incidentally on x-rays during dental exams. On x-rays, they appear as radiopaque masses surrounded by a radiolucent rim. Treatment involves simple surgical removal, with an excellent prognosis and no recurrence.
The document discusses several types of odontogenic tumors that can occur in the jaws. It focuses on describing ameloblastoma, adenomatoid tumor, and calcifying epithelial odontogenic tumor. Ameloblastoma is a benign but locally aggressive tumor arising from odontogenic epithelium. It commonly presents as a painless swelling in the mandible and radiographs show multilocular radiolucency. Histologically there are follicular or plexiform patterns. Adenomatoid tumor is a rare benign tumor associated with impacted teeth. Calcifying epithelial odontogenic tumor is a rare, locally aggressive tumor that can be mistaken for carcinoma, presenting with calcified masses visible on radiographs.
This document discusses odontogenic keratocysts (OKCs), a type of jaw cyst. It covers the classification, causes, histopathology, clinical features, radiographic features, differential diagnosis, treatment principles, and surgical treatment options for OKCs. OKCs most commonly occur in the mandibular molar and ramus areas and are often radiolucent and multilocular in appearance on radiographs. Treatment options include wide surgical excision or marsupialization to prevent recurrence of these cysts which have a high rate of recurrence compared to other jaw cysts.
This document discusses red and white lesions of the oral cavity, focusing on oral candidiasis. It describes the various types of oral candidiasis including pseudomembranous, erythematous, chronic plaque-type, and median rhomboid glossitis. Predisposing factors, clinical findings, diagnosis, treatment with antifungal medications or surgery, and prognosis are summarized for each type. Chronic hyperplastic candidiasis may require long-term antifungal therapy or surgery due to risk of recurrence. Overall prognosis is generally good if predisposing factors can be addressed.
The document discusses the classification of odontogenic cysts. It describes several classification systems proposed over time, including Robinson's classification from 1945, Thoma-Robinson-Bernier classification from 1960, Pindborg and Kramer's classification from 1971, and the WHO classification from 1971 and its update in 1992. The WHO classifications categorize cysts as developmental or inflammatory, and further divide developmental cysts into odontogenic and non-odontogenic types. Shafer's classification also categorizes cysts based on etiology as developmental or inflammatory, and further divides them based on the tissue of origin.
This document discusses radicular cysts, which are the most common inflammatory cysts in the oral cavity. Radicular cysts arise from epithelial residues in the periodontal ligament as a result of periapical periodontitis following pulp necrosis. They are usually asymptomatic but can cause swelling and bone resorption as they expand. The cyst forms from the proliferation of epithelial cell rests in the granulation tissue surrounding the apex of an infected tooth. Histologically, they are lined by stratified squamous epithelium and surrounded by fibrous connective tissue that may contain cholesterol crystals. Treatment involves root canal therapy or extraction with curettage of the cyst lining.
This document discusses fibro-osseous lesions, which replace normal bone with fibrous tissue containing newly formed mineralized structures. It describes several types of fibro-osseous lesions including fibrous dysplasia, cemento-osseous dysplasias like periapical cemental dysplasia, and fibro-osseous neoplasms like ossifying fibroma. For each type, it covers definitions, clinical features, radiographic appearances, differential diagnosis, and treatment approaches.
Calcifying epithelial odontogenic tumor is a rare, aggressive but benign odontogenic tumor accounting for 1% of all odontogenic tumors. It was first recognized by Pindborg and is of epithelial origin. Intraosseous tumors are more common than extraosseous tumors. Radiographically, it appears as a radiolucency that may contain small radiopacities. Surgical removal by enucleation is the treatment of choice, with recurrence rates of 10-15%.
The document discusses different types of cysts that can occur in the oral and maxillofacial region. It defines cysts and classifies them based on their origin and location. It provides details on the pathogenesis, clinical features, radiographic appearance and histology of specific cysts such as dentigerous cysts and odontogenic keratocysts. Dentigerous cysts are defined as cysts originating from the separation of the dental follicle from around the crown of an unerupted tooth. Odontogenic keratocysts are distinctive cysts that arise from cell rests of the dental lamina and have more aggressive behavior than other cysts. Complications of cysts include recurrence, development of
Radicular cysts originate from epithelial cell rests of Malassez and form through three phases: initiation, cyst formation, and growth/enlargement. They are usually painless unless infected and associated with nonvital teeth. Calcifying odontogenic cysts contain ghost cells, which represent abnormal keratinization and have an affinity for calcification. They may also induce dental tissue formation. Keratocystic odontogenic tumors initiate from dental lamina proliferation and enlarge through factors like osmolality, inflammatory exudate, glycosaminoglycans, and collagenolytic/bone resorbing molecules. Their thin fragile linings and intrinsic growth potential contribute to high recurrence rates.
Oral lichen planus is a chronic inflammatory disease that affects the oral mucosa. It is characterized by white striations (Wickham's striae) and varies in appearance from reticular to erythematous or ulcerative lesions. The cause is unknown but involves a cell-mediated immune response. Treatment focuses on reducing symptoms and includes topical corticosteroids, immunosuppressants, or retinoids. Malignant transformation may rarely occur so follow-up is important.
This document discusses mixed odontogenic tumors and odontogenic sarcomas according to the 2005 WHO classification. It provides details on ameloblastic fibroma, its clinical features, histopathology, radiographic features and differential diagnosis. It also discusses ameloblastic fibro-odontoma and fibro-dentinoma, calcifying cystic odontogenic tumor, complex and compound odontomas, and odontoameloblastoma. The key information provided includes the definitions, epidemiology, clinical and radiographic presentation, histopathology, and differential diagnosis of these odontogenic lesions.
This document discusses various mucocutaneous disorders of the oral cavity, including genodermatoses, infective causes, and non-infective conditions. It provides details on specific diseases such as erythema multiforme, pemphigus, and cicatricial pemphigoid. Erythema multiforme is characterized by target lesions that can involve the oral mucosa. Pemphigus is a chronic blistering disease caused by loss of cell adhesion, while cicatricial pemphigoid involves subepithelial blistering that results in scarring.
This document discusses various types of pseudocysts and true cysts found in the body. It begins by defining the key differences between a true cyst and a pseudocyst. Pseudocysts are lined by granulation and/or fibrous tissue rather than an epithelial cell layer. The document then classifies and describes different types of pseudocysts including traumatic bone cysts, aneurysmal bone cysts, and developmental cysts. It provides details on the etiology, location, patient demographics, clinical presentation, radiographic features, histopathology and treatment for each type.
This document describes a case report of a peripheral ossifying fibroma (POF) in a 22-year-old female patient. POFs are non-neoplastic reactive lesions of the gingiva caused by local irritants like plaque or food impaction. Histopathological examination showed fibrous connective tissue with bony trabeculae and dystrophic calcification, consistent with POF. Treatment involves complete surgical excision to remove the lesion and any remaining irritants in order to reduce the risk of recurrence.
This document discusses classifications and clinical relevance of oral epithelial dysplasia in assessing risk of oral potentially malignant disorders. It describes various classification systems for grading dysplasia including WHO and Ljubljana systems. Key histopathological features of dysplasia are loss of maturation and increased nuclear-cytoplasmic ratio. Higher risk of malignant transformation is seen with factors like female gender, long standing lesions, location on tongue/floor of mouth, large size and presence of dysplasia. Accurate grading helps determine prognosis and clinical management.
The document discusses various periodontal instruments used in dental procedures like probing, scaling, root planing, and surgery. It describes the purpose and usage of different types of probes, scalers, curettes, ultrasonic instruments and other tools. Key details about Gracey curettes, sickle scalers, hoe scalers and techniques like adaptation, angulation and strokes are provided.
Regional odontodysplasia is a developmental anomaly affecting the ectodermal and mesodermal components of tooth development, causing teeth to be small, mottled brown, and hypocalcified. It most commonly impacts the central and lateral incisors. Radiographically, affected teeth appear ghost-like with reduced density and large pulp chambers. While the etiology is uncertain, factors like trauma, infection, and vascular defects have been suggested. Clinical diagnosis is based on irregular tooth shape and brown discoloration, while radiographs reveal a shell-like appearance. Treatment typically involves early extraction and prosthetic replacement, though restorative procedures like root canals may attempt to save affected teeth.
This document provides information on vesiculobulllous lesions, including their classification, pathophysiology, diagnosis, types of pemphigus, clinical features, pathogenesis, histopathology, confirmatory diagnosis, differential diagnosis, and treatment. It discusses conditions like pemphigus vulgaris, pemphigoid, paraneoplastic pemphigus. Pemphigus vulgaris involves autoantibodies against desmogleins 1 and 3, causing blistering in skin and mucosa. Paraneoplastic pemphigus is associated with neoplasms and involves multiple organs. Diagnosis involves biopsy, DIF, and ELISA to detect specific autoantibodies.
The document summarizes information about periapical cysts, also known as radicular cysts or apical cysts. It defines a periapical cyst as an odontogenic cyst derived from cell rests of Malassez that proliferate in response to inflammation from pulpal necrosis. Periapical cysts typically present as round radiolucencies associated with the apex of a non-vital tooth. Histologically, they contain a lumen lined by stratified squamous epithelium and surrounded by a fibrous connective tissue wall. Treatment involves extraction of the involved tooth along with cyst enucleation or marsupialization.
This document provides an overview of odontogenic tumors, including their classification and descriptions of common tumors. It discusses key features of ameloblastoma, including clinical presentation, radiographic appearance and histopathological variants. Unicystic and peripheral ameloblastomas are also described. Other tumors covered include adenomatoid odontogenic tumor, calcifying epithelial odontogenic tumor, and compound and complex odontomas. For each tumor, the summary highlights critical information on classification, clinical features, radiology, histopathology and differential diagnosis.
This document discusses different types of odontogenic tumors. It classifies them into three categories: tumors of odontogenic epithelium, mixed odontogenic tumors, and tumors of odontogenic ectomesenchyme. Key tumors discussed include ameloblastoma, adenomatoid odontogenic tumor (AOT), and calcifying epithelial odontogenic tumor (CEOT). Ameloblastoma is the most common odontogenic tumor and can be solid/multicystic, unicystic, or peripheral. AOT typically occurs in younger females in the anterior maxilla. CEOT accounts for less than 1% of odontogenic tumors and resembles cells of the enamel organ or dental lamina.
This document provides information on various odontogenic tumors including:
- Ameloblastoma - A benign but locally aggressive tumor that can cause facial deformities. It has follicular and plexiform histological patterns.
- Calcifying epithelial odontogenic tumor (CEOT) - A locally aggressive tumor consisting of epithelial strands and spheres often accompanied by calcifications. It can be central or peripheral.
- Adenomatoid odontogenic tumor (AOT) - A non-aggressive lesion usually found around crowns of unerupted teeth consisting of epithelial swirls and ducts with calcifications.
The document describes clinical features, radiographic appearances, histological patterns and characteristics of these
1) Ameloblastoma is a benign, locally invasive odontogenic tumor of enamel organ-type tissue that is the second most common odontogenic tumor.
2) It typically presents as a painless swelling in the mandible and is classified based on histological and clinical features into subtypes including follicular, plexiform, unicystic, and peripheral ameloblastoma.
3) Treatment involves surgical resection such as segmental resection for large tumors due to the high recurrence risk with more conservative treatments like curettage or enucleation.
1) Ameloblastoma is a benign, locally invasive odontogenic tumor of enamel organ origin that arises in the jaws. It is classified based on location (central/peripheral), histological subtype (follicular, plexiform, etc.), and clinical behavior (conventional/unicystic).
2) Radiographically, ameloblastoma appears as a multilocular radiolucency with septae, resembling a "soap bubble" or "honeycomb" pattern. Microscopically it consists of islands of odontogenic epithelium resembling dental lamina.
3) Treatment involves wide local excision or segmental resection due to its high recurrence risk. Curettage
This document defines and describes odontogenic tumors, which are neoplasms or tumor-like malformations arising from odontogenic tissues. It classifies various odontogenic tumors based on their origin from odontogenic epithelium, mesenchyme, or mixed tissues. Key tumors discussed include ameloblastoma, adenomatoid odontogenic tumor (AOT), calcifying epithelial odontogenic tumor (CEOT), and ameloblastic fibroma. Clinical features, imaging findings, and histopathological characteristics are provided for each tumor type.
Odontogenic tumors arise from tooth-forming tissues and can be benign or malignant. Ameloblastoma is the most common odontogenic tumor, appearing as a multilocular radiolucency in the mandible of middle-aged patients. It is a benign epithelial tumor consisting of follicles resembling the enamel organ. Other common tumors include ameloblastic fibroma, calcifying epithelial odontogenic tumor, and odontogenic myxoma. These lesions are typically asymptomatic and discovered on routine radiographs.
This document summarizes mixed odontogenic tumors, which contain both odontogenic epithelium and ectomesenchyme. It discusses three main types: ameloblastic fibroma, adenomatoid odontogenic tumor, and odontomas. Ameloblastic fibroma contains odontogenic epithelium and spindled mesenchyme that may resemble dental papilla. It typically occurs in young patients and presents as a painless swelling. Adenomatoid odontogenic tumor is characterized by epithelial duct-like structures and inductive changes in the connective tissue. It has a predilection for the anterior jaws. Odontomas are hamartomas containing fully formed dental tissues. They are the most
Odontogenic tumors arise from tooth-forming tissues and can be divided into three categories: tumors of odontogenic epithelium without mesenchyme, tumors with both epithelium and mesenchyme, and tumors of mesenchyme alone. Ameloblastoma is the most common odontogenic tumor, representing 1% of jaw tumors. It typically presents as a multilocular radiolucency in the mandible and is classified as solid/multicystic, unicystic, or peripheral. Histologically it demonstrates islands of epithelial cells resembling dental lamina. Treatment involves wide local excision due to its persistence and recurrence.
This document discusses various pathologies that can present as pericoronal radiolucencies, including dentigerous cysts, unicystic ameloblastomas, adenomatoid odontogenic tumors, calcifying odontogenic cysts, and ameloblastomas. It provides details on the clinical features, radiographic appearances, and differential diagnosis of these conditions. In particular, it focuses on dentigerous cysts, describing variants such as central, lateral, and circumferential types and emphasizing their association with impacted tooth crowns.
DENTIGEROUS CYST- an odontogenic cyst that surrounds the crown of impacted tooth , develops by fluid accumulation between REE(reduced enamel epithelium) and the enamel surface , resulting in a cyst which the crown located within the lumen.
This document discusses various types of tumors and tumor-like swellings of the jaws, with a focus on ameloblastoma. It defines key terms like tumor, neoplasm, cyst, and classifies odontogenic tumors. It then describes ameloblastoma in detail - the most common odontogenic tumor. It discusses the clinical, radiographic, and histopathological features of various subtypes of ameloblastoma including follicular, plexiform, basal, granular, and desmoplastic. Treatment typically involves wide excision. Unicystic and peripheral variants are also outlined. Rare malignant variants that can metastasize are mentioned.
The document discusses several odontogenic tumors including:
Ameloblastic fibroma is a mixed tumor of odontogenic origin composed of neoplastic epithelium and connective tissue that commonly occurs in children and teenagers. It is often associated with an impacted tooth.
Ameloblastic fibro-odontoma is similar to ameloblastic fibroma but contains neoplastic epithelium, neoplastic myxomatous connective tissue, and foci of enamel and dentin formation.
Odontoma is the most common odontogenic tumor and is considered a hamartoma. It has two types, compound and complex, which are composed of enamel and dentin laid down in an abnormal pattern
This document provides information about ameloblastoma, a benign odontogenic tumor. It discusses the incidence, age, sex, and site prevalence. Typical presentation is a slow-growing, painless swelling of the jaw that causes expansion and thinning of the cortical plates. On radiographs, it appears as a multilocular radiolucency. Histologically, the main subtypes are follicular, plexiform, acanthomatous, and basal cell. Treatment involves complete surgical removal to prevent recurrence, as it is highly radioresistant. Long-term follow-up is necessary given the high recurrence rates with incomplete excision.
There are several subtypes of ameloblastoma including common, unicystic, and peripheral ameloblastomas. Common ameloblastomas typically occur in people aged 20-40 and present as slow-growing lesions in the mandible that cause bone expansion. Unicystic ameloblastomas usually affect younger people aged 16-20 and present as well-defined radiolucencies associated with impacted mandibular third molars. Peripheral ameloblastomas present as nodules in older adults aged 23-82 in the gingiva of the mandible or maxilla. Histologically, the subtypes can be distinguished based on epithelial patterns and features. Treatment involves surgical excision of the lesion and surrounding
The document discusses the management of jaw tumors, including diagnosis, treatment planning, and surgical excision principles. Diagnosis involves history, examination, biopsy, and imaging. Treatment planning considers tumor factors like location, size, and histology. Surgical excision modalities range from conservative enucleation to more aggressive resection, depending on the tumor's aggressiveness, location, size, and duration. The goal is to completely remove the tumor while preserving adjacent structures.
This document discusses various entities that can produce pericoronal radiolucencies, including both those without and with opacities. It describes normal follicular spaces and several pathologies that appear as radiolucencies surrounding unerupted teeth, such as dentigerous cysts, odontogenic keratocysts, and ameloblastic fibromas. It also provides details on inflammatory paradental cysts and pericoronitis. Differential diagnoses and typical management approaches are provided for each condition.
Stem cells can differentiate into other types of cells and divide to produce more stem cells. There are two main types: embryonic stem cells which are pluripotent and can become any cell type but raise ethical issues, and adult stem cells which are multipotent and found in specific tissues where they aid in repair. Stem cell research aims to understand development and treat diseases like Alzheimer's, Parkinson's, diabetes, and spinal cord injuries by replacing damaged cells. Dental stem cells from the pulp have potential for tissue regeneration.
This document discusses methods for decalcifying bone and teeth for histological examination. It begins with an introduction to decalcification and describes the process of removing calcium ions from bone to make it flexible for pathological investigation. It then classifies common decalcifying agents such as acids, chelating agents, and other solutions. The document discusses factors that affect the rate of decalcification and tests used to determine when decalcification is complete. It provides details on processing and staining decalcified bone and teeth. The document concludes with precautions for decalcification and references.
1. Advanced diagnostic techniques such as nucleic acid-based methods like PCR and hybridization methods have overcome limitations of conventional diagnostic methods by being more sensitive, specific, and rapid.
2. PCR exponentially amplifies DNA or RNA sequences, allowing single molecule detection, but cannot differentiate live from dead organisms. Hybridization methods pair complementary nucleic acid strands to detect specific sequences.
3. Other techniques discussed include flow cytometry for analyzing cell properties, Southern blotting for detecting DNA fragments, and ELISA for detecting antibodies or antigens. These techniques have various applications in microbiology, human genetics, forensics, and more.
This document provides information on laboratory diagnosis of fungal infections. It begins with an introduction to mycology and classification of fungi. It then discusses various diagnostic methods for different types of fungal infections, including microscopic examination, culture techniques, biochemical methods, and molecular identification. Specific techniques are described for diagnosing candidiasis, including microscopic morphology, culture characteristics on different media, biochemical profiles, commercially available identification systems, and molecular methods. Sample collection and processing methods are also summarized.
This document discusses oral squamous cell carcinoma (OSCC). It begins with an introduction stating OSCC is the 8th most common cancer in males and 15th in females worldwide. Tobacco, alcohol, HPV infection, iron deficiency, and vitamin deficiencies are identified as risk factors. The document then discusses the pathogenesis of OSCC in more detail for different risk factors. Clinical features, histopathological features, variants of OSCC, and staging are also summarized. References are provided at the end.
This document provides an overview of tuberculosis (TB), including its classification, pathogenesis, forms, diagnosis and treatment. It describes how TB is caused by various mycobacterium species, especially Mycobacterium tuberculosis. TB most commonly affects the lungs but can spread to other organs. Diagnosis involves tests like chest x-rays, sputum smears, cultures and the Mantoux skin test. Treatment involves use of antibiotics like isoniazid, rifampin, pyrazinamide and ethambutol, either as primary treatment or for drug-resistant cases. Immunization with BCG vaccine provides some protection.
Taste is detected by taste buds located in the tongue, soft palate, and throat. Taste buds contain receptor cells that are activated by different tastes like sweet, salty, sour, and bitter. When a taste substance comes in contact with receptor cells, it causes a change in cell permeability that leads to generation of nerve impulses. These impulses travel through cranial nerves to the brainstem and cortex for perception and identification of different tastes. Factors like temperature, hormones, age, and diseases can affect a person's ability to perceive different tastes. Taste helps identify nutritious foods as well as toxic substances.
The periodontal ligament is a specialized connective tissue that connects teeth to the alveolar bone of the jaws. It is composed of cells, collagen fibers, blood vessels and nerves. The collagen fibers are arranged in bundles and attach to both the cementum covering the tooth root and the overlying alveolar bone. The periodontal ligament functions to attach teeth, absorb chewing forces, maintain the position of teeth, and allow limited tooth movement through the remodeling of its collagen fibers.
The glossopharyngeal nerve is the ninth cranial nerve. It is a mixed nerve that originates in the medulla oblongata and exits through the jugular foramen. It carries both sensory and motor fibers and innervates the middle ear, tonsils, back of the tongue, pharynx, and the stylopharyngeus muscle. Damage to the glossopharyngeal nerve can result in loss of sensation in these areas as well as difficulties swallowing and reduced salivation. Glossopharyngeal neuralgia is a condition characterized by severe pain in the throat and ear caused by compression of the nerve.
This document provides an overview of fibro-osseous lesions and focuses on fibrous dysplasia. It discusses the classification, etiology, clinical features, radiographic features, histologic features, treatment and prognosis of fibrous dysplasia. Fibrous dysplasia is a benign bone lesion caused by a mutation in the GNAS1 gene. It can present as monostotic, polyostotic or craniofacial lesions. Radiographically, it appears as radiolucent or radiopaque areas with a "ground glass" appearance. Histologically, it is characterized by fibrous tissue and irregular woven bone trabeculae. Treatment involves surgery or bisphosphonates and the prognosis is generally good
This document discusses various types of cellular adaptations: atrophy, hypertrophy, hyperplasia, metaplasia, dysplasia. Atrophy is a reduction in cell size and number. Hypertrophy is an increase in cell size but not number. Hyperplasia is an increase in cell number. Metaplasia is a change from one adult cell type to another. Dysplasia refers to abnormal cell shapes and sizes that can progress to cancer. Cellular adaptations provide clues for pathologists to diagnose disease.
This document discusses methods for diagnosing dental caries. It begins with definitions of caries and outlines ideal requirements for diagnostic methods. Traditional methods discussed include visual examination, tactile probing, tooth separation, dental floss, and radiography using techniques like intraoral periapical films and bitewing films. Advanced diagnostic tests mentioned include digital radiography, intraoral cameras, laser fluorescence. Recent advances discussed are terahertz imaging, optical coherence tomography, and cone beam computed tomography.
This document discusses dental caries vaccines. It begins by describing primary and secondary immune responses. It then discusses antigenic components of Streptococcus mutans, the main cause of dental caries, including adhesins, glucosyl transferases, and glucan binding proteins. The mechanisms of action and routes of immunization for caries vaccines are presented, including oral, systemic, active gingivo-salivary, and passive routes. Recent advances in caries vaccine development are also summarized, such as sub-unit vaccines, DNA vaccines, plant-derived vaccines, and strain replacement therapy. The conclusion states that as caries vaccines are introduced, the dentist's role will shift from caries management to prevention.
Leonardo DiCaprio Super Bowl: Hollywood Meets America’s Favorite Gamegreendigital
Introduction
Leonardo DiCaprio is synonymous with Hollywood stardom and acclaimed performances. has a unique connection with one of America's most beloved sports events—the Super Bowl. The "Leonardo DiCaprio Super Bowl" phenomenon combines the worlds of cinema and sports. drawing attention from fans of both domains. This article delves into the multifaceted relationship between DiCaprio and the Super Bowl. exploring his appearances at the event, His involvement in Super Bowl advertisements. and his cultural impact that bridges the gap between these two massive entertainment industries.
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Leonardo DiCaprio: The Hollywood Icon
Early Life and Career Beginnings
Leonardo Wilhelm DiCaprio was born in Los Angeles, California, on November 11, 1974. His journey to stardom began at a young age with roles in television commercials and educational programs. DiCaprio's breakthrough came with his portrayal of Luke Brower in the sitcom "Growing Pains" and later as Tobias Wolff in "This Boy's Life" (1993). where he starred alongside Robert De Niro.
Rise to Stardom
DiCaprio's career skyrocketed with his performance in "What's Eating Gilbert Grape" (1993). earning him his first Academy Award nomination. He continued to gain acclaim with roles in "Romeo + Juliet" (1996) and "Titanic" (1997). the latter of which cemented his status as a global superstar. Over the years, DiCaprio has showcased his versatility in films like "The Aviator" (2004). "Start" (2010), and "The Revenant" (2015), for which he finally won an Academy Award for Best Actor.
Environmental Activism
Beyond his film career, DiCaprio is also renowned for his environmental activism. He established the Leonardo DiCaprio Foundation in 1998, focusing on global conservation efforts. His commitment to ecological issues often intersects with his public appearances. including those related to the Super Bowl.
The Super Bowl: An American Institution
History and Significance
The Super Bowl is the National Football League (NFL) championship game. is one of the most-watched sporting events in the world. First played in 1967, the Super Bowl has evolved into a cultural phenomenon. featuring high-profile halftime shows, memorable advertisements, and significant media coverage. The event attracts a diverse audience, from avid sports fans to casual viewers. making it a prime platform for celebrities to appear.
Entertainment and Advertisements
The Super Bowl is not only about football but also about entertainment. The halftime show features performances by some of the biggest names in the music industry. while the commercials are often as anticipated as the game itself. Companies invest millions in Super Bowl ads. creating iconic and sometimes controversial commercials that capture public attention.
Leonardo DiCaprio's Super Bowl Appearances
A Celebrity Among the Fans
Leonardo DiCaprio's presence at the Super Bowl has noted several times. As a high-profile celebrity. DiCaprio attracts
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The notion of Dwayne Johnson kidnapping seems straight out of a Hollywood thriller. Dwayne "The Rock" Johnson, known for his larger-than-life persona, immense popularity. and action-packed filmography, is the last person anyone would envision being a victim of kidnapping. Yet, the bizarre and riveting tale of such an incident, filled with twists and turns. has captured the imagination of many. In this article, we delve into the intricate details of this astonishing event. exploring every aspect, from the dramatic rescue operation to the aftermath and the lessons learned.
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The Origins of the Dwayne Johnson Kidnapping Saga
Dwayne Johnson: A Brief Background
Before discussing the specifics of the kidnapping. it is crucial to understand who Dwayne Johnson is and why his kidnapping would be so significant. Born May 2, 1972, Dwayne Douglas Johnson is an American actor, producer, businessman. and former professional wrestler. Known by his ring name, "The Rock," he gained fame in the World Wrestling Federation (WWF, now WWE) before transitioning to a successful career in Hollywood.
Johnson's filmography includes blockbuster hits such as "The Fast and the Furious" series, "Jumanji," "Moana," and "San Andreas." His charismatic personality, impressive physique. and action-star status have made him a beloved figure worldwide. Thus, the news of his kidnapping would send shockwaves across the globe.
Setting the Scene: The Day of the Kidnapping
The incident of Dwayne Johnson's kidnapping began on an ordinary day. Johnson was filming his latest high-octane action film set to break box office records. The location was a remote yet scenic area. chosen for its rugged terrain and breathtaking vistas. perfect for the film's climactic scenes.
But, beneath the veneer of normalcy, a sinister plot was unfolding. Unbeknownst to Johnson and his team, a group of criminals had planned his abduction. hoping to leverage his celebrity status for a hefty ransom. The stage was set for an event that would soon dominate worldwide headlines and social media feeds.
The Abduction: Unfolding the Dwayne Johnson Kidnapping
The Moment of Capture
On the day of the kidnapping, everything seemed to be proceeding as usual on set. Johnson and his co-stars and crew were engrossed in shooting a particularly demanding scene. As the day wore on, the production team took a short break. providing the kidnappers with the perfect opportunity to strike.
The abduction was executed with military precision. A group of masked men, armed and organized, infiltrated the set. They created chaos, taking advantage of the confusion to isolate Johnson. Johnson was outnumbered and caught off guard despite his formidable strength and fighting skills. The kidnappers overpowered him, bundled him into a waiting vehicle. and sped away, leaving everyone on set in a state of shock and disbelief.
The Immediate Aftermath
The immediate aftermath of the Dwayne Johnson kidnappin
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Introduction
Leonardo DiCaprio, A name synonymous with Hollywood excellence. is not only known for his stellar acting career but also for his impressive real estate investments. The "Leonardo DiCaprio house" is a topic that piques the interest of many. as the Oscar-winning actor has amassed a diverse portfolio of luxurious properties. DiCaprio's homes reflect his varied tastes and commitment to sustainability. from retreats to historic mansions. This article will delve into the fascinating world of Leonardo DiCaprio's real estate. Exploring the details of his most notable residences. and the unique aspects that make them stand out.
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Leonardo DiCaprio House: Malibu Beachfront Retreat
A Prime Location
His Malibu beachfront house is one of the most famous properties in Leonardo DiCaprio's real estate portfolio. Situated in the exclusive Carbon Beach. also known as "Billionaire's Beach," this property boasts stunning ocean views and private beach access. The "Leonardo DiCaprio house" in Malibu is a testament to the actor's love for the sea and his penchant for luxurious living.
Architectural Highlights
The Malibu house features a modern design with clean lines, large windows. and open spaces blending indoor and outdoor living. The expansive deck and patio areas provide ample space for entertaining guests or enjoying a quiet sunset. The house has state-of-the-art amenities. including a gourmet kitchen, a home theatre, and many guest suites.
Sustainable Features
Leonardo DiCaprio is a well-known environmental activist. whose Malibu house reflects his commitment to sustainability. The property incorporates solar panels, energy-efficient appliances, and sustainable building materials. The landscaping around the house is also designed to be water-efficient. featuring drought-resistant plants and intelligent irrigation systems.
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Privacy and Seclusion
Another remarkable property in Leonardo DiCaprio's collection is his Hollywood Hills house. This secluded retreat offers privacy and tranquility. making it an ideal escape from the hustle and bustle of Los Angeles. The "Leonardo DiCaprio house" in Hollywood Hills nestled among lush greenery. and offers panoramic views of the city and surrounding landscapes.
Design and Amenities
The Hollywood Hills house is a mid-century modern gem characterized by its sleek design and floor-to-ceiling windows. The open-concept living space is perfect for entertaining. while the cozy bedrooms provide a comfortable retreat. The property also features a swimming pool, and outdoor dining area. and a spacious deck that overlooks the cityscape.
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The Hollywood Hills house incorporates several green features that are in line with DiCaprio's environmental values. The home has solar panels, energy-efficient lighting, and a rainwater harvesting system. Additionally, the landscaping designed to support local wildlife and promote
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4. INTRODUCTION
Tumors derived from the odontogenic tissues constitute an unusually diverse group
of lesions.
This multiformity reflects the complex development of the dental structures,
since these tumors all originate through some aberration from the normal pattern
of odontogenesis.
5. WHO-Classification-2003
ODONTOGENIC EPITHELIUM
WITHOUT ODONTOGENIC
ECTOMESENCHYME
•Ameloblastoma –
solid/multicystic
•Ameloblastoma –
extraosseous/peripheral
•Ameloblastoma – desmoplastic
•Ameloblastoma - unicystic
•Squamous odontogenic tumour
•Calcifying epithelial odontogenic
tumour
•Adenomatoid odontogenic
tumour
•Keratocystic odontogenic tumour
ODONTOGENIC EPITHELIUM WITH
ODONTOGENIC ECTOMESENCHYME
WITH OR WITHOUT HARD TISSUE
FORMATION
•Ameloblastic fibroma
•Ameloblastic fibrodentinoma
•Ameloblastic fibro-odontome
•Calcifying cystic odontogenic
tumour
•Dentinogenic ghost cell tumour
•Odontoameloblastoma
•Odontomes - complex and
compound
ODONTOGENIC
ECTOMESENCHYME WITH OR
WITH OUT INCLUDED
ODONTOGENIC EPITHELIUM
•Cementoblastoma
•Odontogenic Fibroma
•Odontogenic Myxoma or
fibromyxoma
7. ADENOMATOID ODONTOGENIC TUMOR
HISTOLOGIC DEFINATION:
A hamartomatous lesion of odontogenic epithelium producing solid nodules of
cuboidal or columnar cells, here and there forming convoluted bands arranged in
complicated patterns. Throughout the lesion the cells form structures of
tubular or ductlike appearance. The lesion may be partly cystic with the solid
tumorous tissue constituting part of large cyst wall. The fibrous connective
stroma is rather sparse and may contain dysplastic dentinoid as well as calcified
material that may be quite extensive.
8. AOT-3% - 7%-all odontogenic tumors
Lesion-formerly considered-variant-ameloblastoma & designated
as “adenoameloblastoma-1905-1969,
1969-PHILIPSEN and BIRN introduce term adenomatoid
odontogenc tumor
Investigators-suggested-lesion arises-remnants of dental lamina.
10. CLINICAL AND RADIOGRAPHIC FEATURES:
Younger patients & 2/3rd -10 to 19 years of age.
Anterior portions of the maxilla.
Female prediliction.
Small, sessile masses-facial gingiva-maxilla.
Clinically-cannot be differentiated-common gingival fibrous lesions.
Asymptomatic-routine radiographic examination.
Larger lesions-painless expansion of the bone.
11. 75% of cases-circumscribed, unilocular radiolucency-crown -
unerupted toot- canine.
Follicular type AOT-impossible to differentiate radiographically -
dentigerous cyst.
Less often-well-delineated unilocular radiolucency-not related -
unerupted tooth-located between-roots of erupted teeth
(extrafollicular type).
12. The lesion-completely radiolucent-however, fine (snowflake)
calcifications. This feature may be helpful in differentiating the
AOT- dentigerous cyst.
Peripheral variant-gingival fibroma or epulis-growth-labial-palatal
mucosa.
Slight erosion-alveolar bone-no radiographic change.
13. HISTOPATHOLOGIC FEATURES:
Spindle shaped epithelial cells - sheets, strands, or whorled
masses of cells in a scant fibrous stroma.
Epithelial cells- rosette like structures
Central space- empty or contain small amounts of eosinophilic
material-may stain for amyloid.
Tubular or duct like structures-characteristic feature-AOT, may
be prominent, scanty, or even absent in a given lesion.
These consist -central space surrounded-layer of columnar or
cuboidal epithelial cells.
Nuclei-cells tend-polarized away-central space.
(HE × 160)
14. Mechanism of formation-tubular structures is not entirely clear
but-result-secretory activity-tumor cells, which appear to be
preameloblasts.
These structures-not true ducts & no glandular elements are
present-tumor.
Small foci of calcification-tumor-interpreted as abortive enamel
formation.
Some AOT-larger areas of calcification-interpreted as dentinoid
or cementum. (HE × 200)
15. Another characteristic cellular pattern-
Nodules composed-polyhedral, eosinophilic epithelial cells-squamous
appearance-well-defined cell boundaries & prominent intercellular bridges.
Nuclei may-very mild-pleomorphism.
Islands may contain pools-amorphous amyloid-like material & globular masses
of calcified substances-Resembles CEOT/AOT lesion
CEOT like foci-does not influence growth potential of tumor
16. Yet another epithelial pattern is found between & connecting the cell-
rich nodules & particularly at the tumor periphery.
Pattern-composed- strands of epithelium, one to two cells in
thickness, forming a trabecular or cribriform configuration.
Occasional foci-mitotic activity among AOT tumor cells may be
traced, although-not a prominent feature.
Rare instances melanin pigmentation - both tumor & stroma cells &
presence -melanocytes may be found in AOT’s
17. Occurrence-hyaline, dysplastic dentinoid material or calcified
osteodentin in AOTs-described -several authors.
Dentin or dentinoid containing dentinal tubules is exceedingly
rare.
Stroma-fibrous, mature connective tissue without
ectomesenchymal features,
Production of dysplastic dentinoid is likely - result of-
metaplastic process
Calcified material-varying amounts-most lesions.
Irregular calcified bodies- common-often exhibit-concentric or
Liesegang pattern.
18. IHC
Classical AOT phenotype is characterized by a cytokeratin (CK) profile
similar-follicular cyst and/or oral or gingival epithelium
+ve
• CK5
• CK17
• CK19
-ve
• CK4
• CK10
• CK13
• CK18
20. TREATMENT AND PROGNOSIS:
AOT -completely benign-because of its capsule, it enucleates
easily-bone.
Aggressive behavior has not been documented
Recurrence-Rare
22. Less than 1% of all odontogenic tumor.
Tumor arises -dental lamina remnants.
3rd to 6th decades
Equal sex predilection.
Mandible: maxilla ratio 2:1
23. CLINICAL AND RADIOGRAPHIC FEATURES:
A painless, slow growing swelling
Margins-lytic defect are often scalloped-well defined.
20%-ill-defined periphery &
20% corticated border.
Entirely radiolucent-but calcified structures of varying size &
density.
Calcifications are usually scattered within the tumor.
“Driven-snow” pattern of the calcifications.
27. HISTOPATHOLOGIC FEATURES:
CEOT-islands, strands, or sheets of polyhedral epithelial cells in
a fibrous stroma.
Nuclei-considerable variation & giant nuclei.
Some tumors -nuclear pleomorphism-feature- not considered-
indicate malignancy.
Large areas-amorphous, eosinophilic, hyalinised (amyloid-like)
extracellular material
28. Tumor islands frequently enclose masses-hyaline material-results-
cribriform appearance.
Calcifications-distinctive feature develop-amyloid-like material &
form concentric rings (liesegang ring calcifications).
Tend to fuse & form large-complex masses.
31. Occurrence of Langerhans cells in CEOT
Asano et al & takata et al-another histologic variant of the
intraosseous CEOT -two japanese patients
In both cases the tumor chiefly consisted of scattered small islands
of epithelial cells.
Occasionally several, clear cells positive s-100 protein, iysozome,mt1,
ln-3, and okt6 antibodies, but not for keratin antibody.
Ultrastructurally,s-100-positive cells-identified -langerhans cells
based-rod & tennis racket- shaped birbeck granules.
Some correlation b/n tumor regression & number of langerhans cells.
Langerhans cells in ceots may play a role either in antigen
presentation or in regression of the tumor.
32. Occurrence of myoepithelial cells in CEOT
Ultrastructural findings-CEOT disclosed-two cell populatlons.
One population-classic polyhedral epithelial cells, & other
comprised cells arranged peripherally with elongated profiles &
juxtaposed to tumor epithelial cells.
Latter cells-large number-cytoplasmic fine filaments-similar-
smooth muscle- type cell.
They showed-lamina densa continuous-neighboring epithelial cells
& demonstrated-large number-hemidesmosomes.
33. However, desmosomes b/n these cells & tumor epithelial
cells were not present.
ultrastructural characteristics-cells-interpreted-
myoepithelial cells.
cell type-found-tumors-glandular origin, has not been
described previously-odontogenic tumors & its occurrence-
CEOT has not been confirmed-other electron microscopic
studies.
34. Amyloid-like material-Pindborg tumor-investigated by histochemical,
immunohistochemical, biochemical methods & electron microscopy.
Material generally stains as amyloid (+ve-Congo red or thioflavine T).
After Congo red staining, the amyloid will exhibit apple-green
birefringence when viewed with polarized light.
36. TREATMENT & PROGNOSIS:
CEOT-same biologic behavior-ameloblastoma.
Conservative local resection -include a narrow rim of surrounding bone.
Recurrence rate -15%.
Tumors treated - curettage -highest frequency of recurrence.
Overall prognosis -good.
37. ODONTOGENIC MYXOMA
Myxomas -arise -odontogenic ectomesenchyme.
Close microscopic resemblance - mesenchymal portion-developing tooth.
Soft tissue myxomas -Rare
Intraosseous counterparts- frequently found
Very few intraosseous myxomas -other than the jaws, clavicle, ribs, femur
Intraosseous myxomas are most commonly- jaws & odontogenic in origin.
38. CLINICAL AND RADIOGRAPHIC FEATURES:
Myxomas -25 to 30 years.
No sex predilection.
Mandible -more commonly than maxilla.
Smaller asymptomatic & discovered -radiographic examination.
Larger lesions -painless expansion -involved bone.
Some instances-growth – tumor – rapid
39. Radiographically, unilocular or multilocular radiolucency-displace or
cause resorption-teeth.
Radiolucency - irregular or scalloped, fine trabeculae, some
intersecting at right angles- ‘tennis-racquet’ or ‘step-ladder’.
Large myxomas –mandible- “soap bubble” radiolucent pattern-
indistinguishable from-ameloblastomas.
40. Zhang et al., classified radiographic appearances of OM
into six types:
Type I: Unilocular well-defined radiolucency,
Type II (multilocular): Two or more compartments with multiple
interlaced osseous trabeculae described as honey comb, soap bubble
or tennis racquet radiolucency,
Type III: Lesion located in alveolar bone,
Type IV: Lesion involving the maxillary sinus,
Type V (moth eaten appearance): Larger radiolucent area with
irregular borders,
Type VI: Combination of bone destruction and bone formation giving
sun ray appearance.
41. Pathogenesis
“According to Lucas“-OM-odontogenic tumor-frequent-adolescence-
association-missing or unerupted teeth-sporadic presence of odontogenic
epithelium.
Adekeye et at" reviewed-different arguments-individual tissues-considered-
possible sources of OMs-dental papilla, dental follicle, & periodontal tissues-
as possible "germ centers“
No strong evidence-odontogenic origin could be found except-OM’s -
degenerative form of odontogenic fibroma-Intraosseous neurofibroma, showing
extensive myxomatous changes, would have a number of features in common
OM
42. Lombardi et al-not find similar staining patterns for vimentin &
S-100 protein-OMs compared to dental follicle, dental papilla,&
periodontal ligament cells-
suggesting nonodontogenic origin for the tumor.
Other studies suggested that-
Myofibroblastic origin or
Dual fibroblastic-histiocytic origin.
44. Histochemical study shows-ground substance –composed-
glycosaminoglycans, chiefly hyaluronic acid & chondroitin sulfate.
Immunoreactivity-antibodies directed against vimentin
Focal reactivity- muscle-specific actin.
Immunohistochemically-myxoma cells show diffuse of inactive-appearing
odontogenic epithelial rests maybe scattered throughout the myxoid ground
substance.
(H and E ×40)
45. Epithelial rests are not required-diagnosis & not obvious -most
cases.
Some patients-tumor may-greater tendency-form collagen
fibers-designated as fibromyxomas or myxofibromas.
Myxoma-microscopically confused- myxoid jaw neoplasms:
-Chondromyxoid fibroma or
-Myxoid neurofibroma.
47. TREATMENT AND PROGNOSIS
Small myxomas – curettage.
Reevaluation -at least 5 years.
Larger lesions, more extensive resection-because-not
encapsulated & tend to infiltrate the surrounding bone.
Recurrence rate-25%.
Overall prognosis - good
Metastases do not occur.
48. Conclusion
AOT & CEOT& ODONTOGENIC MYXOMA are of odontogenic origin,
commonly seen in adolescence & are occasionally associated with
unerupted teeth. Hence through knowledge about these lesions is
necessary for proper diagnosis & treatment plan.
49. References
Textbook Of Oral & Maxillofacial Pathology: Neville 1st South Asian Edition
Textbook Of Oral & Maxillofacial Pathology:7th Edition Shafer’s
Adenomatoid Odontogenic Tumor Of The Mandible: Review Of The Literature And
Report Of A Rare Case :Journal Of Head & Face Medicine 2005, Vol 1:3
Calcifying Epithelial Odontogenic Tumor (Pindborg Tumor) Head And Neck Pathol
(2011) 5:137–139
Calcifying Epithelial Odontogenic Tumor :Hindawi Publishing Corporation Journal Of
Case Reports In Pathology Volume 2013
Adenomatoid Odontogenic Tumor, An Uncommon Tumor: Contemporary Clinical
Dentistry | Apr-jun 2012 | Vol 3| Issue 2
Odontogenic Myxoma: National Journal Of Maxillofacial Surgery | Vol 4 | Issue 1
| Jan-jun 2013
Textbook Of Odontogenic Tumors & Allied Lesions: peter.A.Reichart/Hans
P.Philipsen
Editor's Notes
Follicular type AOT sometimes extend apically along the root past the CEJ. This feature may help to distinguish an adenomatoid odontogenic tumor from a dentigerous cyst.
After Congo red staining, the amyloid will exhibit apple-green birefringence when viewed with polarized light.
, although rare examples of malignant or borderline malignant calcifying epithelial odontogenic tumor have been reported, with documented metastasis to regional lymph nodes and lung.
Chondromyxoid fibroma should have areas of cartilaginous differentiation, whereas myxoid neurofibromas tend to have scattered lesional cells that are positive for antibodies directed against S-100 protein.