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30 Cards in this Set
- Front
- Back
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Non-neoplastic proliferation of granulomatous tissue containing multinucleated giant cells & occuring centrally within bone (jaw bone)
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Central Giant Cell Granuloma
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Clinical Features:
->60% under 30 -Female, 70% in mandible -Most: asymptomatic Some: pain, swelling, root displacement -Majority slow-growing |
Central Giant Cell Granuloma
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Radiograph: Well-circumscribed unilocular/multilocular radiolucency
-Mimic periapical granuloma, chronic periodontitis, or ameloblastoma |
Central Giant Cell Granuloma
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Histology:
-number of multinucleated giant cells in ovoid -Giant cells may resemble osteoclasts: numerous uniform nuclei distributed in cytoplasm -Numerous extravasted RBCs |
Central Giant Cell Granuloma
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"Brown tumors" seen from hyperparathyroidism are histologically indistinguishable from this
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Central Giant Cell Granuloma
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Benign (aggressive) neoplasm occuring in epiphyses of long bones
-Rarely occcurs in Jaws -Histologically different from CGCG of Jaws |
(True) Giant Cell Tumor of Bone
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Uncommon developmental condition of jaws showing bilteral enlargement of 2 or 4 quadrants of jaws, maxillary involvement causing slight upturn in the eyes
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Cherubism
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Clinical Features:
-Onset b/t 2 & 5 years -Involves jaws bilaterally, almost always mandible -Enlargement is painless but distorts alveolar ridges, tooth position, occlusion, speech -Enlargement progresses thru puberty but then slows/regress |
Cherubism
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Radiographic:
-Bilateral multiocular radiolucencies of the jaws |
Cherubism
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Histology:
-Number of multinucleated giant cells in fibroblast background -Looks liek CGCG -Eosinophilic cuffing of small blood vessels |
Cherubism
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Non-neoplastic proliferation of granulomatous tissue containing multinucleated giant cells & occuring centrally within bone (jaw bone)
|
Central Giant Cell Granuloma
|
|
Clinical Features:
->60% under 30 -Female, 70% in mandible -Most: asymptomatic Some: pain, swelling, root displacement -Majority slow-growing |
Central Giant Cell Granuloma
|
|
Radiograph: Well-circumscribed unilocular/multilocular radiolucency
-Mimic periapical granuloma, chronic periodontitis, or ameloblastoma |
Central Giant Cell Granuloma
|
|
Histology:
-number of multinucleated giant cells in ovoid -Giant cells may resemble osteoclasts: numerous uniform nuclei distributed in cytoplasm -Numerous extravasted RBCs |
Central Giant Cell Granuloma
|
|
"Brown tumors" seen from hyperparathyroidism are histologically indistinguishable from this
|
Central Giant Cell Granuloma
|
|
Benign (aggressive) neoplasm occuring in epiphyses of long bones
-Rarely occcurs in Jaws -Histologically different from CGCG of Jaws |
(True) Giant Cell Tumor of Bone
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|
Uncommon developmental condition of jaws showing bilteral enlargement of 2 or 4 quadrants of jaws, maxillary involvement causing slight upturn in the eyes
|
Cherubism
|
|
Clinical Features:
-Onset b/t 2 & 5 years -Involves jaws bilaterally, almost always mandible -Enlargement is painless but distorts alveolar ridges, tooth position, occlusion, speech -Enlargement progresses thru puberty but then slows/regress |
Cherubism
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|
Radiographic:
-Bilateral multiocular radiolucencies of the jaws |
Cherubism
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|
Histology:
-Number of multinucleated giant cells in fibroblast background -Looks liek CGCG -Eosinophilic cuffing of small blood vessels |
Cherubism
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Treatment:
-Slow disease: followup Rapid: intervention Prognosis: lesions tend to slow down (by 4th decade) |
Cherubism
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A benign empty or fluid containing cavity within bone that is devoid of an epithelial lining
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Traumatic Bone Cavity
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Etiology:
-Trauma/hemmorage theory: blood clot following trauma does not heal by bone regeneration -Poor venous drainage: buildup of interstitial fluid -Local bone growth disturbance -Ischemic marrow necrosis |
Traumatic Bone Cavity
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Clinical Features:
-Any bone -- but common in jaws -10 & 20 yo -Mandible -Males -80% asymptomatic -Premolar/molar area most common |
Traumatic Bone Cavity
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Radiograph:
-In a dentulous area, characteristically scalloped between roots of the teeth |
Traumatic Bone Cavity
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Diverse group of mostly non-neoplastic conditions that replace normal bone by fibrous tissue.
-Forms new mineralized product: bone, cementum, their precursors or combo -REQUIRES clinical & radiographic features -- histologic exam is not enough |
Fibro-Osseous Lesions of the Jaw
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Deveopmental non-neoplastic but tumor-like condition: normal bone is repalced by cellular fibrous connective tissue containing irregular trabeculae of newly formed bone
---Polyostoic or Monostotic |
Fibrous Dysplasia
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Clinical Features:
-limited to a single bone 80% of all cases -Jaws most common: MAX>mand -Diagnosed 2nd decade of life -M=F -Can involve maxilla & spread to Craniofacial type |
Monostotic Fibrous Dysplasia
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-"Ground Glass" appearance
-Mandible involvement may produce buccolingual expansion & bulging of info border, displacement of mandibular canal -Max involvement: displace maxillary sinus floor -Max involvement: increased radiodensity at base of skull -Narrow PDL with Ill-defined lamina dura (blends with adjacent bone) |
Monostotic Fibrous Dysplaisa of Jaws
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Histologic:
-Trabeculae of immature bone -Curvilinear (chinese character shape) |
Monostotic Fibrous Dysplasia of Jaws
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