Bone Tumors Flashcards

(69 cards)

1
Q

Primary or secondary bone tumor is more common?

A

Primary bone tumors are less common than bone metastases

secondary bone tumors

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2
Q

most common primary bone cancer, ?

A

Osteosarcoma

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3
Q

Osteosarcoma is the most common primary bone cancer, • Then ? And?

A

chondrosarcoma and Ewing sarcoma.

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4
Q

Benign or malignant tumor more common?

A

Benign tumors the commonest, with greatest frequency within the
first three decades of.

  • Bone tumors in elderly persons are much more likely to be
    malignant.
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5
Q

Etiology of bone tumor ?

A

Idiopathic •Genetic syndromes •Bone infarcts, •Chronic osteomyelitis, •Paget disease, • Irradiation. •Fibrous dysplasia • Use of metal orthopedic devices.

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6
Q

Clinical presentation of bone tumors ?

A

•Benign lesions : asymptomatic detected as incidental findings. •Others produce pain or a slowly growing mass
. •Pathologic fracture

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7
Q

Investigations of bone tumor ?

A

•Radiologic imaging •Biopsy

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8
Q

Bone forming primary bone tumors

Benign ? Malignant ?

A
  • Osteoma
    Osteoid osteoma
  • Osteosarcoma
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9
Q

Cartilage Forming
Primary Bone Tumors
B / m

A

Enchondroma/Chondrosarcoma

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10
Q

Fibroblastic Tumors
Primary Bone Tumors

Benign Malignant

A

Fibroma Fibrosarcoma

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11
Q

Undetermined Origin
V Primary Bone Tumors
Locally Malignant

A

Giant Cell Tumor (Osteoclastoma)

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12
Q

Secondary Secondary

A

Metastatic Tumors (The Commonest)

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13
Q

Osteoma

Type of lesion ? Most common site? Age?

A

• Benign lesions • Head and neck, including the paranasal

sinuses, • Can occur elsewhere • Middle age

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14
Q

• Mixture of woven and lamellar bone.

A

Osteoma

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15
Q

Cause local mechanical problems (e.g.,

obstruction of a sinus cavity)

A

Osteoma

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16
Q

Do not undergo malignant transformation

?

A

Osteoma

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17
Q

Osteoid Osteoma and Osteoblastoma

Type of lesion ? Age? Gender ?

A

•Benign neoplasms •The teenage years and 20s, with a male predilection

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18
Q

Osteoid Osteoma and Osteoblastoma

Distinguished from each other, primarily by ?

A

their size, site and clinical presentation.

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19
Q

Arise beneath the periosteum in the proximal femur and tibia or posterior spinal elements ?

A

Osteoid osteomas

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20
Q

Less than 2 cm in diameter ?

A

Osteoid osteomas

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21
Q

Localized pain, most severe at night, relieved by aspirin.

?

A

Osteoid osteomas

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22
Q

Larger than 2 cm ?

A

Osteoblastomas

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23
Q

Involves the spine more frequently ?

A

Osteoblastomas

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24
Q

Cause pain not responsive to aspirin.

?

A

Osteoblastomas

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25
Osteoblastomas | Treatment?
Local excision is the treatment of choice.
26
Malignant transformation is rare | ?
Osteoblastomas
27
Shows radiolucent well-defined area, surrounded by a halo of dense reactive bone -X-ray ?
Osteoid osteomas:
28
Gross: lesions are round-to-oval masses of hemorrhagic gritty tan tissue Type of tumor ?
Osteoid osteomas:
29
Microscopically: Nidus, well circumscribed and composed of randomly interconnecting trabeculae of woven bone that are prominently rimmed by benign looking osteoblasts Type of tumor ?
Osteoid osteoma
30
The stroma surrounding the neoplastic bone consists of loose connective tissue that contains many dilated and congested capillaries. Reactive sclerotic bone surrounding the nidus Type of tumor?
Osteoid osteoma
31
composed of haphazardly interconnecting trabeculae of woven bone that are rimmed by prominent osteoblasts. The intertrabecular spaces are filled by vascularized loose connective tissue.
Osteoid osteoma
32
a bone-producing malignant mesenchymal | tumor. ?
Osteosarcoma
33
Most common primary malignant tumor of bone.
Osteosarcoma
34
Osteosarcoma | Age? Gender/ site ?
75% of patients are younger than 20 years of age. • With a second peak occurring in elderly persons, • Men are more affected than women • Most tumors arise in the metaphyseal region of the long bones of the extremities, • 60% occurring about the knee, 15% around the hip, 10% at the shoulder, and 8% in the jaw.
35
essential for diagnosis of ? The production of mineralized or unmineralized bone (osteoid)
osteosarcoma
36
PATHOGENESIS of Osteosarcoma?
1. RB gene mutations occur in 60% to 70% of sporadic tumors. Hereditary retinoblastomas have a thousand-fold greater risk for development of osteosarcoma 2. p53, a gene whose product regulates DNA repair
37
Radiographic imaging: a large, destructive, mixed lytic and blastic mass Tumor ?
Osteosarcoma
38
The tumor frequently breaks through the cortex and lifts the periosteum, resulting in reactive periosteal bone formation. ?
osteosarcoma
39
X A triangular shadow on the x-ray between the cortex and raised periosteum (Codman triangle) •Spread hematogenously; 10% to 20% pulmonary metastases, Tumor ?
osteosarcoma
40
Spread hematogenously; 10% to 20% pulmonary metastases, | Tumor?
osteosarcoma
41
Secondary osteosarcomas occur in?
older adults most commonly in the setting of Paget disease or previous radiation exposure
42
Vriable. Solid- cystic, soft-bony gritty, gray-white tumors, often exhibiting hemorrhage and cystic degeneration Tumor?
osteosarcoma
43
Malignant polygonal cells (osteoblasts), showing criteria of malignancy (vary in size and shape (pleomorphic), hyperchromatic nuclei; bizarre tumor giant cells and mitoses •Osteoid, eosinophilic, lace-like •The formation of bone by the tumor cells is characteristic
osteosarcoma
44
Histologic appearance, with coarse, lacelike pattern of neoplastic bone (arrow) produced by anaplastic tumor cells. Note the wildly aberrant mitotic figures (arrowheads).
osteosarcoma
45
Osteochondroma | Type ? Gender ?
Benign / More in males
46
Composed of bony projections with cartilagenous cap that arises from the surface of the bone. ?
Osteochondroma
47
• Slow-growing masses . • Incidental findings. • Bone protrusion and pain (pressure on nerves). Tumor ?
Osteochondroma
48
rarely progress to to benign although they may recur if if
Solitary osteochondromas
49
Malignant transformation occurs more frequently in?
in multiple hereditary | osteochondromas.
50
• X-ray: cartilage capped bony growth. The medullary cavity and cortex are continuous with that of bone, growth is away from joint
Osteochondroma
51
Grossly: cartilage cap overlying bone ?
Osteochondroma
52
Microscopically: cartilage cap, composed of hyaline cartilage with active endochondral ossification (similar to that of epiphyseal plate). Bony stalk is formed of cortical lamellar bone.
Osteochondroma
53
Chondrosarcoma | Age? Site /
Old age, 4th-5th decade • At medullary cavity of pelvic bone, shoulder, and ribs;
54
Painful, progressively enlarging masses • Destroys the cortex and forms a soft tissue mass. ?
Chondrosarcoma
55
X ray: Ill-defined, thickened shaft, stippled appearance or ossification of cartilage, cortex infiltrated by tumor.
Chondrosarcoma
56
Gross: Cartilagenous growth, hemorrhage and necrosis
Chondrosarcoma
57
Microscopic: Cartilage cells with variable degree of atypia, calcification, myxoid cartilaginous matrix.
Chondrosarcoma
58
Contain osteoclast-type giant cells | (Osteoclastoma) ?
Giant Cell Tumor
59
Giant Cell Tumor Type of lesion? Age?
It is benign but locally aggressive • 20-40 years of age
60
Giant Cell Tumor | Site?
``` Epiphysis and metaphysis of long bone around knee (distal femur and proximal tibia) • Pain esp. joint pain and pathologic fracture ```
61
Gross • large, Red-brown tumor with cystic degeneration
Giant Cell Tumor
62
Microscopic • Composed of uniform oval mononuclear cells that constitute the proliferating component of the tumor. • Scattered within this background are numerous osteoclast-type giant cells having 100 or more nuclei.
Giant Cell Tumor
63
Necrosis, hemorrhage, hemosiderin deposition, and reactive bone formation are common secondary features.
Giant Cell Tumor
64
Primary malignant small round cell tumors of bone and soft tissue ?
Ewing Sarcoma
65
After osteosarcoma, it is the second most common pediatric bone sarcoma. ?
Ewing Sarcoma
66
Ewing Sarcoma | Age ? Site ?
80% are younger than 20 years. • Painful enlarging mass in the diaphysis of long tubular bones (especially the femur) and the pelvic flat bones. • chemotherapy and surgical excision
67
The commonest bone tumor ?
Metastatic Disease
68
Mostly affecting the axial skeleton (red marrow, rich | vascularity) ?
Metastatic Disease
69
Radiographic: purely lytic lesion (kidney and lung tumors), | osteoblastic (prostatic adenocarcinoma), or mixed
Metastatic Disease