Miscellaneous Tumors Flashcards

(35 cards)

1
Q

What is a Giant Cell Tumor also known as?

A

Giant Cell Tumor is also known as osteoclastoma.

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2
Q

At what age range does Giant Cell Tumor commonly occur?

A

20-40 years.

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3
Q

Which gender is more commonly affected by Giant Cell Tumor?

A

Females (F > M).

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4
Q

Where is Giant Cell Tumor commonly located?

A

Epiphysis of long bones like femur, tibia, and radius.

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5
Q

Can Giant Cell Tumor extend beyond the epiphysis?

A

Yes, it may extend into the metaphysis or joint.

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6
Q

Are Giant Cell Tumors usually solitary or multiple?

A

Majority are solitary.

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7
Q

What are the two cell populations seen in Giant Cell Tumor histology?

A

Multinucleated large osteoclasts and mononuclear stromal cells.

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8
Q

Which cell type in Giant Cell Tumor is neoplastic?

A

Mononuclear stromal cells.

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9
Q

Name one condition with a similar histologic appearance to Giant Cell Tumor.

A

Aneurysmal bone cyst (<20 years)
Brown Tumor of Hyperparathyroidism
Osteosarcoma with giant cells

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10
Q

Name another condition resembling Giant Cell Tumor histology.

A

Brown tumor of hyperparathyroidism (high Ca & PTH).

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11
Q

Which malignant bone tumor can mimic Giant Cell Tumor histology?

A

Osteosarcoma with giant cells.

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12
Q

What is important for diagnosing Giant Cell Tumor besides histology?

A

Clinical and radiographic correlation.

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13
Q

Is the clinical behavior of Giant Cell Tumor predictable or unpredictable?

A

Unpredictable.

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14
Q

Are most Giant Cell Tumors benign or malignant?

A

Most are benign.

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15
Q

Can Giant Cell Tumors be aggressive?

A

Yes, they can be aggressive.

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16
Q

Can Giant Cell Tumors recur after treatment?

A

Yes, recurrence may occur.

17
Q

Can Giant Cell Tumors metastasize?

A

Yes, they may metastasize to the lung.

18
Q

What transformation can occur in Giant Cell Tumor?

A

Sarcomatous transformation.

19
Q

What histologic feature should be checked for sarcomatous transformation?

A

Mitoses in the stromal spindle cells.

20
Q

How is Giant Cell Tumor treated?

A

Surgical curettage or resection

21
Q

hat does PNET stand for?

A

Primitive Neuro-Ectodermal Tumor.

22
Q

What type of cells are seen in Ewing Sarcoma and PNET?

A

Undifferentiated round cells within the marrow cavity (Small Round Blue Cell Tumor).

23
Q

Which gender is more affected by Ewing Sarcoma and PNET?

A

Males (M > F).

24
Q

What is the common age group for Ewing Sarcoma and PNET?

A

Children and teenagers (5-20 years).

25
What is the classic translocation seen in Ewing Sarcoma?
t(11;22) involving the EWS gene.
26
What are the key X-ray findings in Ewing Sarcoma?
Lytic medullary lesion and concentric ‘onion skin’ layering of new periosteal bone.
27
Which bones are commonly affected by Ewing Sarcoma?
Diaphyses of long bones, pelvis, and tibia.
28
What pathological features are associated with Ewing Sarcoma lesions?
Necrosis and hemorrhage.
29
How do tumoral cells behave in Ewing Sarcoma?
They destroy cortex and periosteum and invade surrounding tissues.
30
What microscopic features are seen in Ewing Sarcoma?
Sheets of undifferentiated small round blue cells.
31
What cytoplasmic material is detected in Ewing Sarcoma and with what stain?
PAS positive material consistent with glycogen.
32
What structure indicates neural differentiation in Ewing Sarcoma?
Homer-Wright rosettes.
33
What are the clinical features of Ewing Sarcoma?
Mass, pain, and local inflammation.
34
What is the treatment for Ewing Sarcoma?
Chemotherapy, surgery, and possibly irradiation.
35
What is the 5-year survival rate for localized Ewing Sarcoma?
0.75