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Diseases of Jaws and Maxillary Sinus
Assoc. Professor Jan Laco, MD, PhD
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Diseases of jaws and maxillary sinus
2. Temporomandibular joint 3. Maxillary sinus
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1a. Genetic diseases Osteogenesis imperfecta Achondroplasia
Cleidocranial dysplasia Cherubism
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1a. Genetic diseases Osteogenesis imperfecta “brittle bone disease“
AD inheritance defect of biosynthesis of collagen I thin bones without cortex - fragile multiple fractures dwarfism + blue sclera + deafness
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1a. Genetic diseases Achondroplasia
most common genetic skeletal disease 75 % cases sporadic mutation FGFR3 gene mutation short-limbed dwarf with normal trunk and head failure of cartilage proliferation in epiphyses protrusive mandible malocclusion
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1a. Genetic diseases Cleidocranial dysplasia
defective formation of clavicles retrusion of maxilla delayed eruption of permanent teeth
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1a. Genetic diseases Cherubism
AD inheritance, mutation of SH3BP2 gene (chr. 4p16.3) boys painless symmetrical swelling of angle of mandibles ± maxillae ± eyes turned upwards begins at 2-4 years rapid growth until puberty regression RTG: symmetrical multilocular radiolucencies Mi: fibrous tissue + hemorrhage + multinucleated giant cells + woven bone treatment: none x conservative (recurrence)
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1b. Metabolic diseases Hyperparathyroidism Rickets
primary (hyperplasia / adenoma of PTG) secondary (hyperplasia of PTGs in renal failure) RTG: multilocular cyst-like areas Mi: similar to giant cell granuloma and cherubism Rickets vitamin D deficiency during bone development infancy wide fontanels + bossing of frontal and parietal eminences Gigantism and acromegaly mandibular condyle prognathism + macroglossia
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1c. Diseases of unknown origin
Paget´s disease of bone Fibro-osseous lesions
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1c. Diseases of unknown origin
Paget´s disease of bone (osteitis deformans) past middle age common RTG finding x clinically silent ? ethiology (paramyxovirus) ? axial skeleton skull – vault + maxilla jaws: symmetric enlargement of alveolar processes + fusion of teeth with hypercementosis to sclerotic bone difficult extraction
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1c. Diseases of unknown origin
Paget´s disease of bone (osteitis deformans) resorption (osteoclasts) irregular new bone formation (osteoblats) Mi: irregular mosaic bone trabeculae + osteoblasts and osteoclasts + vascularity result: thick spongy bone + marrow fibrosis complication: osteosarcoma (rare) treatment: calcitonin and/or bisphosphonates
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1c. Diseases of unknown origin
Fibro-osseous lesions Fibrous dysplasia monostotic polyostotic McCune-Albright´s syndrome Ossifying fibroma (controversial) conventional – y, mandible juvenile trabecular – 10 y, maxilla juvenile psammomatoid – 20 y, paranasal sinuses (Cemento) Osseous dysplasia periapical (cemental) osseous dysplasia focal (cemental) osseous dysplasia florid (cemental) osseous dysplasia familial gigantiform cementoma
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1c. Diseases of unknown origin
Monostotic fibrous dysplasia painless, poorly circumscribed bone swelling in childhood or adolescence (10-30Y) F : M ... 1:1 maxilla malocclusion RTG: replacement of trabecular bone by ground-glass (orange-peel) texture + NO clear demarcation mutation of GNAS1 gene encoding α-subunit of G-protein self-limiting, usually no treatment required rare complication - osteosarcoma
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1c. Diseases of unknown origin
Polyostotic fibrous dysplasia several bones, 50% pts. develop lesions of jaws F : M … 3:1 McCune-Albright´s syndrome poly FD + skin pigmentations + sexual precocity Mi: fibrous tissue + woven bone trabeculae without osteoblast linings
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1c. Diseases of unknown origin
Cemento-osseous dysplasia hamartomatous lesions in vicinity of roots of vital teeth ? of periodontal ligament origin ? same process x differ clinically in extent and RTG incidental findings (dif. dg. ossifying fibroma) periapical cemento-osseous dysplasia F : M … 10 : 1 asymptomatic lesion anterior mandible (lower I + few adjacent teeth) RTG: radiolucent (~ periapical granuloma) radiopaque
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1c. Diseases of unknown origin
focal cemento-osseous dysplasia similar to periapical OD x molar teeth florid cemento-osseous dysplasia non-expansile, 2 or more jaw areas middle-aged Black females familial gigantiform cementoma expansile, 2 or more jaw areas, autosomal dominant Mi: cellular fibrous tissue + trabeculae of woven / lamelar bone + cementum-like material calcification
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1d. Inflammations acute osteomyelitis chronic osteomyelitis
alveolar osteitis
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1d. Inflammations Acute osteomyelitis sources predispositions
periapical infection, open fractures predispositions fractures, radiation damage, Paget disease, leukemia, DM oral anaerobes (Bacteroides, Porphyromonas), mixed infection adult males – mandible, rarely neonates - maxilla clinically severe deep-seating pain, swelling, teeth tenderness, red swollen gingiva, anaesthesia of lower lip, regional lymphadenopathy, fever + leucocytosis RTG: ill-defined radiolucent areas (10th day)+ dense sequestra
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1d. Inflammations Acute osteomyelitis
suppurative inflammation in marrow spaces compression of blood vessels (thrombosis) bone necrosis sequestrum subperiostal area subperiostal abscess perforation fistulas to skin and oral mucosa complete restoration possible granulation tissue fibrous tissue fibrous bone compact bone remodelation treatment: ATB + debridement complications: fracture chronic osteomyelitis
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1d. Inflammations Chronic osteomyelitis Chronic focal sclerosing OM
inadequate treatment of acute osteomyelitis de novo by low-grade infection complication of irradiation Mi: scant fibrous tissue with chronic inflammation + fragments of dense bones tissue (mosaic, necrotic) Chronic focal sclerosing OM uncommon, young people with carious lower M1 RTG: radiopaque area below tooth root Diffuse sclerosing OM old Black people, superinfection of florid OD
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1d. Inflammations Chronic osteomyelitis with productive periostitis (Garré´s OM) uncommon response to chronic periapical low-grade infection young people, carious lower M1 reactive new bone formation
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1d. Inflammations Alveolar osteitis (dry socket)
most common painful complication of tooth extraction sources excessive extraction trauma, low blood supply, local anaesthesia, oral contraceptives, after radiotherapy after extraction of M3 (less vascularized bone), females few days after extraction, mucosa around red and tender destruction of clot by fibrinolytic enzymes – infection and food in contact with bone bone necrosis sequestra treatment: irrigation of mild hot antiseptics
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1e. Cysts Odontogenic Non-odontogenic Pseudocysts solitary bone “cyst“
aneurysmal bone “cyst“
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1e. Pseudocysts Solitary bone “cyst“ (simple, traumatic)
? etiology unknown F : M … 3 : 2 < 25 years painless swelling of mandible frequently no content RTG: cavity expands between teeth roots Mi: NO epithelial lining + wall: fibrous tissue may regress spontaneously treatment: surgical opening and closure (healing by fibrous tissue follows)
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1e. Pseudocysts Aneurysmal bone “cyst“ exceedingly rare in jaws
? etiology unknown between 10 – 20 years painless swelling of mandible RTG: multilocular radiolucency Mi: many blood-filled spaces without lining + wall: fibrous tissue + giant cells treatment: curettage recurrence
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1. Diseases of jaws 1a. Genetic diseases 1b. Metabolic diseases
1c. Diseases of unknown origin 1d. Inflammations 1e. Cysts 1f. Tumors
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1f. Tumors Odontogenic Non-odontogenic
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Non-odontogenic tumors
Primary: benign x malignant bone cartilage other Secondary: metastases
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Non-odontogenic tumors
Benign primary tumors osteoma osteochondroma central giant cell granuloma ossifying fibroma - rare hemangioma - rare
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Non-odontogenic tumors
Osteoma x Exostosis torus palatinus: posterior midline of hard palate torus mandibularis: lingual aspect of mandible opposite to mental foramen, bilateral hard swelling Mi: compact or cancellous bone Gardner´s syndrome - AD inheritance multiple osteomas + polyposis coli malignancy
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Non-odontogenic tumors
Osteochondroma “cartilage-capped osteoma“ hard bony protuberance coronoid or condylar process joint dysfunction
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Non-odontogenic tumors
Central giant cell granuloma (lesion) benign hyperplastic lesion, developmental ???, reparative ??? < 20 years F : M … 2 : 1 anterior mandible, painless swelling RTG: rounded cyst-like area Mi: vascular fibrous tissue + giant cells + bleeding + hemosiderin treatment: curettage recurrence after incomplete removal
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Non-odontogenic tumors
diff. dg. of giant cell lesions in jaws giant cell granuloma hyperparathyroidism cherubism giant cell tumor of bone (osteoclastoma) aneurysmal bone cyst
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Non-odontogenic tumors
Ossifying fibroma uncommon mandibular premolar or molar area F : M … 2 : 1, 20-40Y painless swelling, ± capsule RTG: radiolucent + opaque with well-defined margins Mi: variable cellular fibrous tissue + woven / lamellar bone + cementum-like material treatment: enucleation variants: juvenile trabecular – children, rapid growth, maxilla juvenile psammomatoid – walls of sinonasal cavities
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Non-odontogenic tumors
Osteosarcoma malignant common primary non-odontogenic neoplasm irradiation, Paget´s disease years, males body of mandible irregular firm swelling developing in months painfull RTG: irregular bone destruction Mi: osteoid formation + atypical osteoblasts + cartilage + fibrous tissue
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Non-odontogenic tumors
Osteosarcoma rapid local growth + early metastases (lungs) treatment: radical surgery 50% recurrence within 1st year 5-year survival: % ( 5 cm)
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Non-odontogenic tumors
Chondrosarcoma 45 years anterior maxilla (60%) painful irregular swelling RTG: radiolucency Mi: cartilage tissue with pleomorphic, binucleated chondrocytes + mitoses locally aggressive + metastases (lungs) treatment: radical surgery (radioresistant)
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Non-odontogenic tumors
Rare tumors Ewing´s sarcoma Multiple myeloma Langerhans cell histiocytosis
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Non-odontogenic tumors
Secondary tumors – hematogenous metastases breast lung prostate thyroid kidney
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Jaw necrosis bisphosphonate osteonecrosis osteoradionecrosis
complication of radiotherapy insufficient previous dental care
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Bisphosphonate osteonecrosis
bisphosphonates (↓ bone resorption), denosumab jaw necrosis + mucosal defect – ulceration previous injury in oral cavity – tooth extraction, … nonhealing painful ulcer on alveolar mucosa + necrosis bone at bottom (sequestrum) + inflammation 2/3 cases … mandible diff. dg.: tumors, chronic osteomyelitis treatment: ATB + sequestrotomy
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Diseases of jaws and maxillary sinus
2. Temporomandibular joint 3. Maxillary sinus
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2. Temporomandibular joint
Trismus - inability to open mouth fully joint inflammation injuries tetanus Ankylosis - permanent limitation of movement fibrosis (irradiation) congenital trauma acute pyogenic arthritis condylar tumors oral submucosal fibrosis, systemic sclerosis
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2. Temporomandibular joint
Osteoarthritis metabolic defect of art. cartilage - defective old people pain, minimal symptoms
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2. Temporomandibular joint
Rheumatoid arthritis - multisystemic disease autoantibodies (rheumatoid factors) females, years symmetrical involvement of smaller joints crepitation, little pain inflammation of synovia - granulation tissue (pannus) Osteochondroma Condylar hyperplasia cranial giant cell arteritis pain on mastication (jaw claudication)
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Diseases of jaws and maxillary sinus
2. Temporomandibular joint 3. Maxillary sinus
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3. Maxillary sinus Inflammation - sinusitis
acute x chronic x hypersensitive rhinogenic x odontogenic periapical inflammation of P or M long oro-antral communication pain + percussion sensitivity
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3. Maxillary sinus Inflammation
Mi: respiratory epithelium squamous metaplasia thickened basal membrane infiltrate - acute - neutrophils - chronic - lymphocytes + plasma cells - hypersensitive - eosinophils
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3. Maxillary sinus Oro-antral communication after extraction of P or M
nose-blowing test root or tooth in sinus prolaps of antral mucosa
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3. Maxillary sinus Antral cysts from mucous glands asymptomatic
disappear spontaneously odontogenic cysts radicular, residual
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3. Maxillary sinus Tumors squamous cell carcinoma males > 50 years
advanced stage – local spread nose obstruction, nose bleeding paresthesia of infraorbital nerve visual disturbances poor prognosis
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