NON- ODONTOGENIC TUMORS Flashcards

(34 cards)

1
Q

Fibro- osseous lesion

Mandible

A

Ossifying Fibroma

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2
Q

Radiographic appearance of Ossifying Fibroma

A

RDL / Mixed lucent - opaque

Well- circumscribed or sharply defined border

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3
Q

‼️‼️BE‼️‼️

Microscopic / Histopath of Ossifying Fibroma

A

📌Fibrous CT
📌Immature , new bone
📌Osteoblast

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4
Q

Tx. Ossifying Fibroma

A

Surgical Excision

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5
Q

DDx. of Ossifying Fibroma

A

Fibrous Dysplasia

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6
Q

Fibro- Osseous Lesiom

A

Fibrous Dysplasia

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7
Q

‼️BE‼️

Clinical Features of Fibrous Dysplasia

A

Maxilla

Malignant transformation to osteosarcoma

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8
Q

‼️BE‼️

Classification of Fibrous Dysplasia

A

Monostotic

Polyostotic

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9
Q

one bone more commn

A

Monostotic

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10
Q

More than one, McCune Albright Syndrome

A

Polyostotic

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11
Q

McCune Albright Syndrome TRIAD

A

Polyostotic fibrous dysplasia
Cafe au lait spot
Early Sexual Development / Hyperfunctioning

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12
Q

normal fibrous tissue
abnormal bone
immature bone

A

Ossifying Fibroma

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13
Q

normal bone

abnormal fibrous tissue

A

Fibrous Dysplasia

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14
Q

Most common bone tumor
widened PDL space
Rx: Sunray/ Sunburst Appearance

A

Osteosarcoma

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15
Q

Radiographic Appearance of Fibrous Dysplasia

A

RDL or mixed lucent opaque
Ground glass appearance
Poorly circumscribed/ poorly defined border

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16
Q

Microscopic / Histopath Fibrous Dysplasia

A

Fibrous CT
Immature new bone chinese character
Osteoblasts
Capillaries

17
Q

Ground Glass Appearance

A

📌Hyperparathyroidism
📌Albers - Schonberg
📌 Fibrous Dysplasia

18
Q

Tx of Fibrous Dysplasia

A

Small lesions- none

Large lesions- surgical recontouring after puberty

19
Q

DDx. of Fibrous Dysplasia

A

Ossifying fibroma

20
Q

benign tumor of mature bone

21
Q

Classification of Osteoma

A
  1. Periosteal

2. Endosteal/ Solitary 📌📌📌 more common

22
Q

Location: Mandible
aAbnormal :bone
Rx: Well circumscribed
Hx: Cellular

A

Ossifying fibroma

23
Q

Location: Maxilla
Abnormal: Fibrous
Rx: Poorly circumscribed
Hx: w/ capillaries vascular

A

Fibrous Dysplasia

24
Q

Gardner’s Syndrome / Familial Colorectal Polyposis (IF EMOS)

A
Intestinal Polyps (Colorectal Carcinoma)
Fibroma
Epidermal Cyst
Multiple Osteoma
Odontoma
Supernumerary Teeth
25
‼️‼️BE | Radiographic of Gardners Sundrome/ Familial Colorectal Polyposis
Radioapaque always | Cotton Wool Appearance
26
Compact bone or Cancellous Bone | Osteoblasts
Microscopic / Histopath Gardners
27
Intestinal Polyposis macules flat, skin pigmentatiom Normal dentition
Peutz Jegher Syndrome
28
‼️‼️BE seem exclusively in the jaws mandible (anterior to the molars)
Central Giant Cell Granuloma
29
between 1st molar & incisors . ant. to the molars between incisor & molars
Central Giant cell granuloma / PGCG
30
Rx. Central Giant Cell Granuloma
RDL
31
Microscopic / Histopath of Gardner Syndrome /Familial Colorectal Polyposis
Fibroblasts Multinucleared giant cells (osteoclast-like) Well vascularized stroma
32
Multinucleared Giant Cell (HAC PC)
``` Hyperparathyroidism Aneurysmal bone cyst Cherubism PGCG Central Giant Cell Granuloma ```
33
📌Hemorrhage
Hemosiderin (breakdown of RBC) ➡️ Hemoglobin Heme➡️ Porphyrin➡️ Biliverdin➡️ Bilirubin ➡️ Hemosiderin
34
allergic rxn, Parasitic infection Viral infection
Eosinophils