Lesions Associated with Impacted Tooth
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Applications of Cytokeratin Expression in the Diagnosis of Oral Diseases
Jemds.com Review Article Applications of Cytokeratin Expression in the Diagnosis of Oral Diseases Archana Sonone1, Alka Hande2, Madhuri Gawande3,Swati Patil4 1, 2, 3, 4 Department of Oral Pathology and Microbiology, Sharad Pawar Dental College, Datta Meghe Institute of Medical Sciences (Deemed to Be University) Sawangi (Meghe), Wardha, Maharashtra, India. ABSTRACT All mammalian cells have a complex intracytoplasmic cytoskeleton made up of three Corresponding Author: main structural units and related proteins, tubulin containing microtubules, actin Dr. Archana Sonone. Department of Oral Pathology and containing microfilaments, and Intermediate Filaments (IF). There are six types of Microbiology, Sharad Pawar Dental IFs; cytokeratin fibres consisting of type I and type II IFs. Cytokeratins (CK), College, Datta Meghe Institute of Medical . comprising of collections of IFs that are explicitly communicated by epithelial tissues Sciences (Deemed to Be University) There are 20 unique polypeptides of CK expressed by epithelium that have been Sawangi (Meghe), Wardha, Maharashtra, indexed based on their molecular weight (range 40-70 kDa). India. CK and associated filaments give a framework to epithelial cells and tissues to E-mail: [email protected] maintain their structural integrity. Thus, ensure mechanical resilience, sustain stress, establish cell polarity, and to protect against variations in hydrostatic pressure. DOI: 10.14260/jemds/2021/50 Genetic encoding of cytokeratins shows homogeneous “nucleotide sequence”. 54 How to Cite This Article: genes are responsible for encoding of cytokeratin in humans which are congregated Sonone A, Hande A, Gawande M, et al. on chromosome no. 2. Genetic mutation of cytokeratins is important for Applications of cytokeratin expression in pathophysiology of various mucocutaneous disorders, which is mostly autosomal the diagnosis of oral diseases. -
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 . -
Iii Bds Oral Pathology and Microbiology
III BDS ORAL PATHOLOGY AND MICROBIOLOGY Theory: 120 Hours ORAL PATHOLOGY MUST KNOW 1. Benign and Malignant Tumours of the Oral Cavity (30 hrs) a. Benign tumours of epithelial tissue origin - Papilloma, Keratoacanthoma, Nevus b. Premalignant lesions and conditions: - Definition, classification - Epithelial dysplasia - Leukoplakia, Carcinoma in-situ, Erythroplakia, Palatal changes associated with reverse smoking, Oral submucous fibrosis c. Malignant tumours of epithelial tissue origin - Basal Cell Carcinoma, Epidermoid Carcinoma (Including TNM staging), Verrucous carcinoma, Malignant Melanoma. d. Benign tumours of connective tissue origin : - Fibroma, Giant cell Fibroma, Peripheral and Central Ossifying Fibroma, Lipoma, Haemangioma (different types). Lymphangioma, Chondroma, Osteoma, Osteoid Osteoma, Benign Osteoblastoma, Tori and Multiple Exostoses. e. Tumour like lesions of connective tissue origin : - Peripheral & Central giant cell granuloma, Pyogenic granuloma, Peripheral ossifying fibroma f. Malignant Tumours of Connective tissue origin : - Fibrosarcoma, Chondrosarcoma, Kaposi's Sarcoma Ewing's sarcoma, Osteosarcoma Hodgkin's and Non Hodgkin's L ymphoma, Burkitt's Lymphoma, Multiple Myeloma, Solitary Plasma cell Myeloma. g. Benign Tumours of Muscle tissue origin : - Leiomyoma, Rhabdomyoma, Congenital Epulis of newborn, Granular Cell tumor. h. Benign and malignant tumours of Nerve Tissue Origin - Neurofibroma & Neurofibromatosis-1, Schwannoma, Traumatic Neuroma, Melanotic Neuroectodermal tumour of infancy, Malignant schwannoma. i. Metastatic -
Oral Pathology and Oral Microbiology
3.3.2 SYLLABUS ( Including Teaching Hours.) MUST KNOW 109 HRS 1 Developmental Disturbances of oral and paraoral structures 03 HRS Developmental disturbances of hard tissues: -dental arch relations, -disturbances related to - -size,shape,number and structure of teeth, -disturbances related to eruption and shedding. Developmental disturbances of soft tissues: Lip,palate,oral mucosa,gingival,tongue and salivary glands Craniofacial anomalies 2 Benign and Malignant tumors of oral cavity 25 HRS Potentially Malignant Disorders of epithelial tissue origin. -Definitions and nomenclature -Epithelial dysplasia -Lesions and conditions:leukoplakia, erythroplakia,oral lichen planus and oral submucous fibrosis. Benign tumors of epithelial tissue origin. - Squamous papilloma, Oral nevi. Malignant tumors of epithelial tissue origin. -Oral squamous cell carcinoma: Definition and nomenclature,etiopathogenesis, TNM staging ,Broder’s and Bryne’s grading systems. -Verrucous carcinoma -Basal cell carcinoma: Definition etiopathogenesis and histopathology -Malignant melanoma: Definition etiopathogenesis and histopathology Benign and malignant tumors of connective tissue -Fibroblast origin:oral fibromas and fibromatosis,peripheral ossifying fibroma peripheral giant cell granuloma, pyogenic granuloma and Fibrosarcoma -Adipose tissue origin:Lipoma -Endothelial origin(blood and lymphatics: Hemangiomas and lymphangiomas, Hereditary hemorrhagic telangiactasia, Kaposi’s sarcoma Bone and cartilage: Chondroma,osteoma,osteoid osteoma, benign osteoblastoma, osteosarcoma, -
Oral Pathology Final Exam Review Table Tuanh Le & Enoch Ng, DDS
Oral Pathology Final Exam Review Table TuAnh Le & Enoch Ng, DDS 2014 Bump under tongue: cementoblastoma (50% 1st molar) Ranula (remove lesion and feeding gland) dermoid cyst (neoplasm from 3 germ layers) (surgical removal) cystic teratoma, cyst of blandin nuhn (surgical removal down to muscle, recurrence likely) Multilocular radiolucency: mucoepidermoid carcinoma cherubism ameloblastoma Bump anterior of palate: KOT minor salivary gland tumor odontogenic myxoma nasopalatine duct cyst (surgical removal, rare recurrence) torus palatinus Mixed radiolucencies: 4 P’s (excise for biopsy; curette vigorously!) calcifying odontogenic (Gorlin) cyst o Pyogenic granuloma (vascular; granulation tissue) periapical cemento-osseous dysplasia (nothing) o Peripheral giant cell granuloma (purple-blue lesions) florid cemento-osseous dysplasia (nothing) o Peripheral ossifying fibroma (bone, cartilage/ ossifying material) focal cemento-osseous dysplasia (biopsy then do nothing) o Peripheral fibroma (fibrous ct) Kertocystic Odontogenic Tumor (KOT): unique histology of cyst lining! (see histo notes below); 3 important things: (1) high Multiple bumps on skin: recurrence rate (2) highly aggressive (3) related to Gorlin syndrome Nevoid basal cell carcinoma (Gorlin syndrome) Hyperparathyroidism: excess PTH found via lab test Neurofibromatosis (see notes below) (refer to derm MD, tell family members) mucoepidermoid carcinoma (mixture of mucus-producing and squamous epidermoid cells; most common minor salivary Nevus gland tumor) (get it out!) -
Head and Neck Pathology Traditional Prognostic Factors
314A ANNUAL MEETING ABSTRACTS Design: 421 archived cases of EC(1995-2007) were reviewed and TMAs prepared Conclusions: Positive GATA3 staining is seen in all vulvar PDs. GATA3 staining is as per established procedures. ERCC1 and RRM1 Immunofl uorescence stains were generally retained in the invasive component associated with vulvar PDs. GATA3 is combined with Automated Quantitative Analysis to assess their expression. The average more sensitive than GCDFP15 for vulvar PDs. Vulvar PDs only rarely express ER and of triplicate core expression was used to determine high and low score cutoff points PR. Vulvar PD should be added to the GATA3+/GCDFP15+ tumor list. using log-rank test on overall survival(OS). Association between expression profi les and clinicopathological parameters was tested using Fisher’s exact test. The independent prognostic value of ERCC1 and RRM1 was tested using Cox model adjusted for Head and Neck Pathology traditional prognostic factors. Results: 304(72%) type-I EC cases and 117(38%) type-II EC cases were identifi ed. Caucasian women had higher proportion of type-I tumors(p<0.001) while elderly women 1297 Subclassification of Perineural Invasion in Oral Squamous Cell were more likely to have type-II tumors (p<0.001). ERCC1 and RRM1 expression was Carcinoma: Prognostic Implications observed in 80% of tumors (336 cases 335 cases,respectively). Kaplan Meier curves K Aivazian, H Low, K Gao, JR Clark, R Gupta. Royal Prince Alfred Hospital, Sydney, showed statistically signifi cant difference in OS between low and high expression of New South Wales, Australia; Royal Prince Alfred Hospital, Sydney, Australia; Sydney ERCC1 and RRM1. -
Compound Odontoma in the Anterior Maxilla
Oncology and Radiotherapy © 1 (46) 2019: 043-045 • CASE REPORT Compound odontoma in the anterior maxilla Ramesh Kunusoth1, Vikas Sahu1, Afreen Fathima2, Rathod Prakash1, Sampath Kumar Pala1, Kotya Naik Maloth3 1 Department of Oral and Maxillofacial Surgery, MNR Dental College and Hospital, Telangana, India 2 Department of Oral Medicine and Radiology, MNR Dental College and Hospital, Telangana, India 3 Department of Oral Medicine and Radiology, Mamata Dental College and Hospital, Telangana, India Odontomas are commonly reported in the dental literature, as they arise from odontogenic epithelium referred to as a mixed INTRODUCTION odontogenic tumor. It is considered to be hamartomas rather than the tumor, characterized by an abnormal calcified mass of dental Background SUMMARY tissues like enamel, dentin, pulp, and cementum. World Health Organization (WHO) classified odontoma into two types, compound Odontoma is a developmental anomaly and considered and complex types based on radiological features. The exact etiology is unknown, but based on the literature postulated causes included to be hamartomas rather than the tumor, characterized by an local trauma, infection, and genetic mutations. Clinically represented abnormal calcified mass of dental tissues like enamel, dentin, as asymptomatic swelling and pain secondary to infection. Here, we report a case of compound odontoma in the anterior maxilla in 20 pulp, and cementum. It is the most comment mixed odontogenic years female patient. tumor occurring in the oral cavity, resulting in the progression Key words: compound odontoma, hamartoma, odontogenic tumor of completely differentiated epithelial and mesenchymal cells, which appear normal or defect in structure [1, 2]. Address for correspondence: Odontoma term is used to denote lesions that contain all Ramesh Kunusoth, Department of Oral and Maxillofacial Surgery, MNR Dental College and Hospital, MNR Nagar, Fasalwadi, Sangareddy, the dental tissues such as enamel, dentin, pulp, and cementum Telangana, 502294, India, email: [email protected] [3]. -
Abstracts of the XXI Brazilian Congress of Oral Medicine and Oral Pathology
Vol. 117 No. 2 February 2014 Abstracts of the XXI Brazilian Congress of Oral Medicine and Oral Pathology ORAL PRESENTATIONS GERMANO, MÁRCIA CRISTINA DA COSTA MIGUEL, ÉRICKA JANINE DANTAS DA SILVEIRA. UNIVERSIDADE AO-01 - MAXILLARY OSTEOSARCOMA INITIALLY FEDERAL DO RIO GRANDE DO NORTE. RESEMBLING PERIAPEX DENTAL INJURY: CLINICAL Renal osteodystrophy represents the musculoskeletal mani- CASE REPORT. JOANA DOURADO MARTINS, JARIELLE festations resulting from metabolic abnormalities in patients with OLIVEIRA MASCARENHAS ANDRADE, JULIANA ARAUJO chronic renal failure (CRF). Woman, 23, reported a hard, asymp- LIMA DA SILVA, ALESSANDRA LAIS PINHO VALENTE, tomatic, expansive mass present for 4 years on the right side of the MÁRCIO CAMPOS OLIVEIRA, MICHELLE MIRANDA face that was causing airway compromise and facial disfigurement. LOPES FALCÃO, VALÉRIA SOUZA FREITAS. UNI- Her history included idiopathic CRF, and she had been receiving VERSIDADE ESTADUAL DE FEIRA DE SANTANA. hemodialysis for 10 years. During this period she developed sec- Maxillary osteosarcoma is a rare and aggressive bone tumor ondary hyperparathyroidism that was managed with total para- that can initially resemble a periapical lesion. Man, 42, came to the thyroidectomy. Computed tomography revealed marked osseous Oral Lesions Reference Center at UEFS complaining of “tooth expansion on the right side of the maxilla and discrete expansion numbness and swollen gums” and loss of sensation in the anterior on the right side of mandible and cranial base. The clinical diag- teeth. His history included previous endodontic emergency treat- nosis was brown tumor. Incisional biopsy led to a diagnosis of ment of units 1.1 and 2.1. The extraoral examination demonstrated renal osteodystrophy. -
Odontoameloblastoma: a Report of a Rare Case
Case Report Odontoameloblastoma: A report of a rare case Karpagaselvi Sanjai1, Bhavna Pandey2, Divya Shivalingaiah1, Harish Muniswamy Kumar1 1Vydehi Institute of Dental Sciences and Research Centre, Bengaluru, Karnataka, 2Department of Oral Pathology, Chettinad Dental College and Hospital, Kanchipuram, Tamil Nadu, India Abstract Odontoameloblastoma (OA) is an uncommon mixed odontogenic tumor that contains an ameloblastomatous component and odontoma-like elements, usually seen to occur in the mandible of younger patients. Radiographically, the tumor shows central destruction of bone with extension of cortical plates and calcified structures which have the radiopacity of tooth structure. These may resemble miniature teeth similar to a compound odontoma or occur as large masses of calcified material similar to a complex odontoma. We report a case of a 17-year-old male with a hard solitary, diffuse swelling over the right lower third of the face for 8 months. Histopathological sections of tumor mass showed diverse and characteristic features of ameloblastoma along with odontogenic epithelium proliferation in unrestrained manner so as to resemble developing tooth bud in stages of morphodifferentiation, apposition and calcification. A diagnosis of OA was made. Hemimandibulectomy was performed on the patient and he remains disease free till today. Keywords: Ameloblastic odontoma, ameloblastoma, complex odontoma, odontoameloblastoma, odontogenic tumor Address for correspondence: Dr. Karpagaselvi Sanjai, Vydehi Institute of Dental Sciences and Research Centre, 82, EPIP Area, Nallurahalli, Bengaluru ‑ 560 066, Karnataka, India. E‑mail: [email protected] Received: 01.09.2017, Accepted: 18.06.2018 INTRODUCTION in both structure and behavior. Due to the presence of odontogenic ectomesenchyme, inductive changes take The combination of two odontogenic tumors is seldom place leading to the formation of dentin and enamel in seen in the field of odontogenic tumors. -
47 Peripheral Compound Odontoma: a Rare Case Report
International Journal of Medicine Research International Journal of Medicine Research ISSN: 2455-7404; Impact Factor: RJIF 5.42 www.medicinesjournal.com Volume 2; Issue 3; May 2017; Page No. 47-50 Peripheral compound odontoma: A rare case report 1 Mariem Meddeb, 2 Sameh Sioud, 3 Chiraz Baccouche, 4 Mounir Omami, 5 Jemil Selmi 1, 2, 4, 5 Department of Medicine and Oral Surgery of the Dentistry Clinic of Monastir, Tunisia 3 Departmen of Dental Anatomy of The Dentistry Clinic of Monastir, Tunisia Abstract Odontomas are the most common odontogenic tumors. They are considered to be hamartomatous malformation rather than true neoplasm. They develop from epithelial and mesenchymal components of the dental apparatus, producing enamel and dentin. Clinically, they may be classified as intraosseous and peripheral odontomas. Although most of the odontomas are asymptomatic, yet these are often associated with tooth eruption disturbances and malocclusion. Keywords: odontoma, peripheral, compound Introduction Odontomas, one of the most common benign odontogenic tumors of epithelial and mesenchymal origin. They are considered actually as hamartomas or developmental anomalies composed of enamel, dentin, cementum and pulp tissue [1]. Peripheral or soft tissue odontomas, those arising in the soft tissue, are rare, judging from the paucity in the literature, or are rarely reported. This excludes those that were in the bone and subsequently erupted [2]. The aim of this article is to report clinical case of compound peripheral odontoma which be diagnosed and treated at the department of Medicine and Oral Surgery of the Dentistry Clinic of Monastir, Tunisia. Case report A 12 year-old male patient with no notable medical history; referred by the pediatric dentistry department for bone Fig 1 swelling in relation to the maxillary left lateral incisor.