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MSK-Derm by Minnie > SM 230a - Neoplasia > Flashcards

SM 230a - Neoplasia Flashcards

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Dermatology Board Prep flashcards
1
Q

What kind of bone tumor is this?

A

Osteosarcoma (malignant)

Look for the Codman Triangle

  • New sub-periosteal bone that raises the periosteum away from the bone
  • This leads to a sunburst reaction
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2
Q

Which tissue is shown in this picture?

A

Bone marrow

Contains adipocytes and hematopoietic stem cells

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3
Q

What kind of bone tumor is this?

How do you know?

A

Multiple myeloma

  • Lots of plasma cells undergoing clonal proliferation
  • Kappa cells only; no lambda
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4
Q

Describe osteoid osteomas

  • Benign or malignant:
  • Typical patient:
  • Common sites:
  • Significance:
A

Osteoid osteoma

  • Benign or malignant: Benign
  • Typical patient: Young adult (<25), M>F
  • Common sites: Cortex of long bones (esp. femur)
  • Significance: Excellent prognosis after nidus removal
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5
Q

What bone tumor is this?

How do you know?

A

Fibrous dysplaisa (benign)

  • Expansile, well-circumscribed lesion
  • Variable internal density
  • May have “ground glass” appearance
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6
Q

Describe the histologic findings of osteoid osteoma

A

Sclerotic bone surrounding a nidus

The nidus = anastomosing woven bone + osteoblastic rimming + vascular stroma

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7
Q

Describe an osteochondroma

  • Benign or malignant:
  • Typical patient:
  • Common sites:
  • Significance:
A

Osteochondroma

  • Benign or malignant: Benign
  • Typical patient: Males <25 y/o
    • ​May arise after trauma or radiation
  • Common sites: Distal femur, proximal tibia, arises from metaphysis
  • Significance: Most common benign bone tumor
    • ​Good prognosis - rarely transforms to a chondrosarcoma
      • Cap > 2 cm suggests malignant transformation
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8
Q

Describe the treatment of osteosarcoma

A
  • Preoperative chemotherapy
    • 2-6 cycles
  • Tumor excision + histologic examination
    • <90% tumor necrosis = consider changing chemo + local therapy if margins are positive
    • >90% tumor necrosis = continue chemo + local therapy if margins are positive
  • Fit for prosthesis
  • Postoperative chemotherapy
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9
Q

Which bone tumors are most likely to arise in the epiphysis?

A

Giant cell tumors (benign)

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10
Q

What kind of bone tumor is this?

A

Multiple myeloma

  • Multiple punched out lesions
  • Caused by clonal proliferation of plasma cells
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11
Q

Which bone tumors are most likely to arise in the metaphysis?

A
  • Malignant
    • Osteosarcoma
    • Chondrosarcoma
  • Benign
    • Endochondoma
    • Osteochondroma
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12
Q

Which benign bone lesion?

“<2cm, appears in long bones, responds to NSAIDs”

A

Osteoid osteoma

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13
Q

Which tumors appear in bone marrow?

A
  • Myeloma
  • Malignant lymphoma

Both are malignant

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14
Q

“CRAB” findings of

HyperCalcemia, Renal insufficiency, Anemia, and lytic Bone lesions

are characteristic of which malignant bone tumor?

A

Multiple myeloma

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15
Q

All statements are true of osteochondroma except:

  1. Recurrences may occur if the cartilaginous cap is not completely excised.
  2. Radiologically and grossly, the tumor projects away from the joint space.
  3. The cartilaginous cap exhibits microscopic features similar to the cartilage composing the growth plate.
  4. Presence of a cartilaginous cap >2cm, especially in an adult, is worrisome for sarcomatous transformation.
  5. In Multiple Hereditary Exostoses (Osteochondromatosis), the incidence of malignant transformation of the cartilaginous cap is over 50%
A

E.

In Multiple Hereditary Exostoses (Osteochondromatosis), the incidence of malignant transformation of the cartilaginous cap is over 50%

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16
Q

Which benign bone lesion?

“Linked to developmental arrest of bone”

A

Fibrous dysplasia

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17
Q

Which bone tumor is shown in this image?

A

Chondroma (benign)

Expansile lytic lesion with calcified matrix

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18
Q

What kind of cartilaginous tumor is this?

A

Chondroma

  • Nodules of mature cartilage within a fatty bone marrow
  • Low cellularity, lack of pleomorphism (just mature cartilage)
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19
Q

What is the characteristic features of a bone tumor that has metastasized from another site?

A

Usually osteolytic (punched-out lesion)

Exception = prostate carcinoma: osteoblastic lesion

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20
Q

Which malignant bone tumor is caused by clonal proiferation of plasma cells?

A

Multiple myeloma

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21
Q

What kind of bone tumor is shown in this x-ray?

A

Osteochondroma

  • Cartilagionous cap on a bony stalk continuous with the medulla of the bone
  • Looks like an ice cream cone
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22
Q

What kind of bone tumor is this?

A

Giant cell tumor of the bone

  • Many multinucleated giant cells
    • May look like osteoclasts
  • Giant cells have lots of nuclei, lots of cytoplasm
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23
Q

Which benign bone lesion?

“<2cm, appears in long bones, does not respond to NSAIDs”

A

Osteoblastoma

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24
Q

Which bone tumors are most likely to arise in the middle of the diaphysis of the bone?

A
  • Benign
    • Fibrous dysplasia
  • Malignant
    • Ewing sarcoma
    • Myeloma
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25
Q

What bone tumor is this? How do you know?

A

Fibrous dysplasia

  • All elements of bone are present, but they are not maturing
  • Irregularly-shaped “C” and “S” shaped spicules of woven bone
    • Without osteoblastic rimming
  • Spindled and collagenous stroma
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26
Q

What kind of bone tumor is this?

A

Ewing Sarcoma (malignant)

  • Diaphysis of long bones (esp. femur)
  • Cortical destruction: “onion skin” pattern
  • Some soft tissue extension
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27
Q

Which benign bone lesion?

“Appears commonly in the medulla of small bones in the hands and feet”

A

Chondroma

28
Q

Describe Multiple Myeloma

  • Benign or malignant:
  • What:
  • Typical Patient:
  • Common sites:
  • Prognosis:
A
  • Benign or malignant: Malignant
  • What: Clonal proliferation of plasma cells (IgG) -> “punched out” lesions
  • Typical Patient: Males 65-70 y/o
  • Common sites: ​Vertebra, ribs, skull, pelvic bones, femur
  • Prognosis: Poor
29
Q

Describe Ewing sarcoma

  • Benign or malignant:
  • What:
  • Typical patient:
  • Common sites:
  • Prognosis:
A

Ewing Sarcoma

  • Benign or malignant: Malignant
  • What: Neuroectodermal tumor of the bone
  • Typical patient: Males <20 y/o
    • ​Suspect Ewing Sarcoma in any bone lesion in boys <15 y/o
    • Caused by t(11:22) that creates fusion protein EWS-FLI1
  • Common sites: Diaphysis of long bones
    • ​Femur, pelvis, ribs
  • Prognosis: Non-metastatic = 60-80%, metastatic = 20%
    • ​Metastasis occurs in 20-25% of cases
30
Q

What kind of bone tumor is this?

A

Osteoid osteoma

31
Q

What are the risk factors for developing osteosarcoma?

A
  • Familial retinoblastoma
  • Li-Fraumeni syndrome (germ line P53 mutation)
  • Paget disease of the bone
  • Bone infarct
  • Radiation
32
Q

Which tissue is shown in this picture?

(The pink part)

A

Bone

33
Q

What kind of tumor is this?

A

Chondrosarcoma (malignant)

  • Cartilage matrix w/ stipplied and arc&ring calcifications
  • Cortical destruction
  • Zero or minimal periosteal reaction
34
Q

What kind of tumor is this?

A

Giant cell tumor of the bone

  • Soap-bubble appearance
  • Lytic lesions in the epiphysis
35
Q

Malignant proliferation of osteoblasts results in what tumor?

A

Osteosarcoma (malignant)

36
Q

Describe the radiographic findings of an osteoma

A

Same density as thte surrounding bone

Made from dense, compact bone

37
Q

Which tumors appear in bone?

A
  • Benign
    • Osteoma
    • Osteoid osteoma
    • Osteoblastoma
  • Malignant
    • Osteosarcoma
38
Q

What kind of bone tumor is this?

A

Chondrosarcoma (malignant)

  • Multiple chondrocytes in each lacunae
  • More cellular than normal cartilage
  • Higher-grade tumors will be very cellular; very little matrix
    • Matrix that is there is poorly differentiated
39
Q

Describe osteosarcoma

  • Benign or malignant:
  • What:
  • Typical patient:
  • Common sites:
  • Prognosis:
A

Ostosarcoma

  • Benign or malignant: Malignant
  • What: Malignant proliferation of osteoblasts
  • Typical patient: 10-20 y/o or >65 y/o
  • Common sites: Metaphysis of long bones, soft tissue usually involved
    • ​Distal femur
    • Proximal tibia
    • Proximal humerus
  • Prognosis: Dependent on response to pre-operative chemo
40
Q

What kind of malignant bone tumor is a “neoplasm of chondrocytes?”

A

Chondrosarcoma

41
Q

All statements are true of osteosarcoma except:

  1. In the vast majority of cases, the radiologic appearance of conventional osteosarcoma mimics other benign osseous tumors.
  2. A relatively higher percentage of pelvic and craniofacial osteosarcomas occur in patients over the age of 30 years.
  3. By definition, an osteosarcoma is a tumor in which bone matrix is produced by malignant mesenchymal cells.
  4. Patients exhibiting at least a 90% histological response to chemotherapy have a much improved survival rate compared with patients who show less than 90% response.
  5. In children, osteosarcoma is a more commonly encountered primary bone tumor than chondrosarcoma
A

A

In the vast majority of cases, the radiologic appearance of conventional osteosarcoma mimics other benign osseous tumors.

This is false; osteosarcomas have a characteristic “Codman Triangle”

42
Q

What is the most common bone tumor?

A

Metastases from other sites

Most common primary bone tumor:

Multiple myeloma

(Osteosarcoma is second)

43
Q

Which benign bone lesion is equally common in males and females?

A

Chondroma

44
Q

Which benign bone lesion is more common in females than males?

A

Giant cell tumors of the bone

45
Q

Which bone tumors are most likely to arise on the edge of the diaphysis of the bone?

A

Osteoid osteoma (benign)

46
Q

Which bone tumor is characterized by a “bony stalk with a cartilaginous cap?”

A

Osteochondroma

47
Q

Which tumors appear in cartilage?

A
  • Benign
    • Osetochondroma
    • Chondroma
    • Chondroblastoma
    • Chondromyxoid fibroma
  • Malignant
    • Chondrosarcoma
48
Q

Describe Osteoma

  • Benign or malignant:
  • Age of onset:
  • Common sites:
  • Significance:
A

Osteoma

  • Benign or malignant: Benign if solitary
  • Age of onset: Middle age
  • Common sites: Surface of facial bone
  • Significance: Little, unless they block the sinus cavity
    • Multiple = increased suspicion for gardner syndrome
49
Q

Which benign bone lesion?

“Appears in the epiphysis of long bones, soap-bubble appearance of x-ray”

A

Giant cell tumor of the bone

50
Q

Describe giant cell tumors of the bone

  • Benign or malignant:
  • Typical patinet:
  • Common sites:
  • Significance:
A
  • Benign or malignant: Benign
  • Typical patinet: 20-40 yo, F > M
  • Common sites: Epiphysis of long bones, esp. knee
  • Significance: Locally aggressive, benign. May recur
51
Q

Which benign bone lesion?

“benign, solitary, slow growing, and commonly appears on the surface of facial bone”

A

Osteoma

52
Q

Describe a chondroma

  • Benign or malignant:
  • Typical patient:
  • Common sites:
  • Significance:
A

Chondroma

  • Benign or malignant: Benign
  • Typical patient: 2nd - 4th decades, M = F
  • Common sites: Medulla of small bones of hands and feet
  • Significance: Observe with radiographs, can be removed with curettage
53
Q

If a patient has Café-au-lait spots and a bone histology that shows irregularly contoured spicules of woven bone without osteoblastic rimming, which syndrome would you suspect?

A

McCune-Albright sydrome

Suspect in polyostic fibrous dysplasia;

Also look for endocrine dysfunction

54
Q

Which malignant bone tumor?

“Common in boys <15 years old”

A

Ewing Sarcoma

55
Q

What kind of bone tumor is characterized by
“nocturnal bone pain releived by aspirin”

A

Osteoid osteoma

56
Q

Describe Fibrous Dysplasia

  • Benign or malignant:
  • Typical patient:
  • Common sites:
  • Significance:
A

Fibrous Dysplasia

  • Benign or malignant: Benign
  • Typical patient: First 3 decades of life
  • Common sites: Femur (single bone)
    • Polyostic may present as McCune-Albright sydrome
  • Significance: Linked to localized developmental arrest
    • ​All normal structures are present, but they do not differentiate into mature structures
57
Q

What are the differences between an osteoblastoma and an osteoid osteoma?

A
  • Osteoblastoma
    • >2 cm
    • Vertebrae
    • Does not respond to NSAIDs
  • Osteoid osteoma
    • <2 cm
    • Long bone (femur)
    • Responds to NSAID
      • “Nocturnal pain releived by apirin”

Note: Both occur commonly in males <25 years old

58
Q

Describe the radiographic findings of osteoid osteoma

A

Radiolucent central focus of woven bone with a vascular stroma.

Surrounding cortical bone is thickened

59
Q

Which bone tumor causes cortical destruction in an “onion skin” pattern?

A

Ewing Sarcoma

60
Q

Describe a Chondrosarcoma

  • Benign or malignant:
  • What:
  • Typical patient:
  • Common sites:
  • Prognosis:
A

Chondrosarcoma

  • Benign or malignant: Malignant
  • What: Neoplasm of chondrocytes
  • Typical patient: M>F, Decades 5-7
  • Common sites: Central portion of the skeleton, within the medullary cavity
    • ​Pelvis, shoulder, rib
  • Prognosis: Depends on grade and surgical accuracy
    • ​Metastases are rare and occur late
61
Q

Which malignant bone tumor?

“Bimodal age, prognosis depends on response to pre-operative therapy”

A

Osteosarcoma

62
Q

What kind of bone tumor is this?

Is it benign or malignant?

A

Osteochondroma - benign

  • Arises from the metaphysis
  • Usually in the distal femur or proximal tibia
  • Bone + cartilaginous cap; continuous with the medullary cavity

Note; cartilaginous cap suggests malignant transformation

63
Q

What kind of bone tumor is this?

A

Osteosarcoma (malignant)

  • Malignant cells directly produce osteoid/woven bone
  • Highly cellular - cells are highly pleomorphic
64
Q

What bone tumor is this?

How do you know?

A

Ewing Sarcoma

  • Diffuse proliferation of small, neoplastic cells
  • May have focal necrosis
  • Cells have rounded nuclei with very little cytoplasm
65
Q

A 10 year-old male has a destructive lytic lesion of the proximal femur. Needle core biopsy of the lesion shows small cells with high nucleocytoplasmic ratio and clear cytoplasm.

Which is the true statement regarding this lesion?

  1. Large cell lymphoma is a common primary bone tumor in this age group.
  2. This tumor sample should be sent for analysis of a specific translocation.
  3. Cytoplasm of this cells do not have glycogen.
  4. Tumor is adequately treated with surgery alone.
  5. Cartilage is commonly formed by the tumor cells.
A

B

This tumor sample should be sent for analysis of a specific translocation.

  • This is Ewing’s sarcoma. Caused by t(11;22) creating fusion protein EWS-FLI1
    • Thank you @NathanShlobin!
  • Translocation analysis will confirm the diagnosis
  • Initial clinical suspicion due to:
    • Long bone tumor in male <15 y/o
    • Histologic findings of small cells with high nucleocytoplasmic ratio
66
Q

Describe the appearance of a chondroma on x-ray

A

Exapansile lytic lesion with a calcified matrix

67
Q

What bone tumor is associated with a translocation [t(11:22)] that creates a fusion protein?

A

Ewing Sarcoma

Fusion protein = EWS-FLI1

MSK-Derm by Minnie (48 decks)

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