Tumours of Bone Flashcards

1
Q

Osteochondroma B/M? (exotosis)

A

Benign

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2
Q

Chondroma B/M?

A

Benign

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3
Q

Osteoid osteoma B/M?

A

Benign

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4
Q

Chondroblastoma B/M?

A

Benign

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5
Q

Osteochondroma (exotosis)

A

Cartilage capped bony projection arising on external surface of bone containing a marrow cavity that is continuous with that of the underlying bone.

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6
Q

Chondroma

A

Low power - lobules of varying sizes

Chondrocytes with small, round, pyknotic nuclei inside hyaline cartilage – no atypia.

Variable cellularity

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7
Q

Osteoid production is essential for diagnosis of what?

A

Osteosarcoma?

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8
Q

What is essential for diagnosis of osetosarcoma?

A

Osteoid production

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9
Q

Are small peripheral lesions more likely to be benign or malignant that large axial regions?
(endochondroma)

A

Small peripheral lesions are more likely to be benign than large axial lesions.
(endochondroma)

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10
Q

Dull pain
Worse at night
Characteristically relieved by aspirin or non-steroidal anti-inflammatory drugs

A

Osteoid osteoma

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11
Q

Radiolucent nidus surrounded by reactive sclerosis in cortex of bone

A

Osteoid osteoma

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12
Q

Prognosis of osteoid osteoma

A

Will resolve without treatment in an average of 33 months.

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13
Q

Osteoid osteoma

A

benign osteoblastic tumour

central core of vascular osteoid

peripheral zone of sclerotic bone

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14
Q

Cartilage capped bony projection arising on external surface of bone containing a marrow cavity that is continuous with that of the underlying bone

A

Osteochondroma

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15
Q

Which age group are affected by ostochondromas?

A

Young <20

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16
Q

Benign hyaline cartilage tumour arising in medullary cavity of bones of hands and feet?

A

Chondroma

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17
Q

Multiple enchondromas are associated with multiple angiomas?

A

Maffucis syndrome

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18
Q

Chondrocytes with small, round, pyknotic nuclei inside hyaline cartilage

A

Chondroma

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19
Q

Must differentiate chondroma from what?

A

Chondrosarcoma

-small peripheral lesions are more likely to be benign that large axial lesions

20
Q

Distinct clinical picture of dull pain that is worse at night and disappears within 20-30 minutes o treatment with NSAIDS

A

Osteoid osteoma

21
Q

Radiolucent nidus surrounded by reactive sclerosis in cortex of bone?

A

Osteoid osteoma

22
Q

benign osteoblastic tumour
central core of vascular osteoid
peripheral zone of sclerotic bone

A

Osteoid osteoma

23
Q

How long does it take for an osteoid osteoma to resolve?

A

Average of 33 months

24
Q

Benign cartilage tumour arising in bone - rare

Can occasionally exhibit more aggressive course

Found at epiphysis of long bones

Age group – second decade of life

A

Chondroblastoma

25
Spherical and well-defined osteolytic foci, sometimes extending into the subarticular bone, joint space or metaphysis
Chondroblastoma
26
Distinct cytoplasmic borders with foci of “chicken-wire” calcification. Closely packed polygonal cells plus areas of immature chondroid. Mitotic activity is low
Chondroblastoma
27
Treatment for chondroblastoma
Biopsy and curettage plus adjuvant liquid nitrogen
28
Where are giant cell tumours often found?
Site - long bones, often around the knee
29
Multinucleated giant cells in a sea of round to oval mononuclear cells
Giant cells
30
Irregular spicules of mineralised bone and osteoid surrounded by osteoblasts Vascular stroma with pleomorphic spindle cells Osteoid and woven bone are seen
Osteoid osteoma
31
Very rare tumour arising from notocord remnants (midline tumour, often in sacral region)
Chordoma
32
Soft, blue-gray, lobulated tumours Gelatinous translucent areas and often a capsule is present Lesion often tracks along nerve roots in the sacral plexus or out the sciatic notch in planes of least resistance.
Chordoma
33
On plain x-ray - appear as a solitary mid-line lesion with bony destruction Often an accompanying soft tissue mass Approximately half of the time focal calcifications are present CT and MRI scans help demonstrate the soft tissue component
Chordoma
34
Lobules and fibrous septa. The malignant cell has eosinophilic cytoplasm & prominent vacuoles of mucus push the nuclei to the side
Chordoma
35
Commonest primary malignant tumour
Osteosarcoma
36
Malignant osteoblasts forming osteoid
Osteosarcoma
37
Age group affected by osteosarcoma?
Young adults, 60% <25 years old
38
Condition which can predispose to osteosarcoma in older patients?
Pagets
39
The second commonest primary malignant tumour of bone Exhibits pure hyaline cartilage differentiation Composed of malignant chondrocytes
Chondrosarcoma
40
Malignant nodules of chondrosarcoma infiltrate between the lamellar bone obliterating the marrow Separation of the nodules by fibrous bands would be another feature highly suggestive of malignancy.
Chondrosarcoma
41
Peripheral primitive neuroectodermal tumour (PNET)
Ewing's sarcoma | -Most common in second decade of life
42
Small round blue cells
Ewing's sarcoma
43
Surgery Radiation therapy Chemotherapy with vincristine, dactomycin and cyclophosphamide Post-operative adjuvant chemotherapy
Ewing's sarcoma
44
Malignant proliferation of plasma cells in bone marrow Occurs in old age Often causes renal failure Results in bone destruction of axial skeleton
Multiple myeloma
45
Cancers which can metastasise to bone?
Thyroid, breast, lung (particularly small cell), kidney prostate Other cancers: gastric cancer, malignant melanoma and neuroblastoma
46
Which type of lung cell cancer may metastasise to bone?
Small cell