Malignant Bone Tumors Flashcards

1
Q

What is the most frequent primary bone malignancy, exclusive of hematopoietic malignancies?

A

Osteosarcoma

Osteosarcoma is particularly common in patients aged 10 to 25 years.

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2
Q

What age group is primarily affected by osteosarcoma?

A

Patients between 10 to 25 years of age, with another peak after 40

Osteosarcoma is exceptionally rare in preschool children.

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3
Q

What percentage of all osteosarcomas do osteosarcomas of the jaws represent?

A

6-8%

These are most often found in the 3rd to 4th decade of life.

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4
Q

What are common symptoms of jaw osteosarcoma?

A

Swelling and pain

Other features may include loosening of teeth, parasthesia, and nasal obstruction.

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5
Q

Which regions of long bones are most commonly affected by osteosarcoma?

A

Metaphyseal region, particularly the lower end of the femur, upper end of tibia, and upper end of humerus

Less commonly, they are found in flat bones such as craniofacial bones, pelvis, and scapula.

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6
Q

What are the predisposing factors for osteosarcoma?

A
  1. Paget’s disease
  2. Radiation exposure
  3. Chemotherapy
  4. Pre-existing benign bone lesions
  5. Foreign bodies

Examples include fibrous dysplasia and orthopedic implants.

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7
Q

What is the mean age for patients with osteosarcoma of the jaw?

A

About 33 years

This is 10 to 15 years older than the mean age for osteosarcomas of the long bones.

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8
Q

What radiographic feature is common in jaw osteosarcoma?

A

Classical sunburst or sunray appearance

This appearance is due to osteophytic bone production on the surface of the lesion.

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9
Q

What is a key histopathological feature for diagnosing osteosarcoma?

A

Detection of osteoid and calcified osteoid produced by tumor cells

Osteoid is recognized by its eosinophilic-staining quality and glassy appearance.

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10
Q

How are osteosarcomas subclassified?

A
  1. Osteoblastic
  2. Chondroblastic
  3. Fibroblastic

These subtypes do not have any prognostic significance.

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11
Q

What is the prognosis for osteosarcoma of the jaw compared to those in long bones?

A

Less aggressive and lower grade

Metastases are seen less frequently, with 30-50% survival rates.

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12
Q

What is a chondroma?

A

Benign tumors composed of mature hyaline cartilage

Commonly located in short tubular bones of the hands and feet.

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13
Q

What is the peak age for the diagnosis of chondromas?

A

3rd to 4th decade of life

They usually present as painless slow-growing lesions.

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14
Q

What is the treatment for a diagnosed chondroma in the jaw?

A

Radical resection

Chondromas in the jaw should be considered potential chondrosarcomas.

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15
Q

What is a chondrosarcoma?

A

A malignant tumor characterized by the formation of cartilage by tumor cells

Chondrosarcoma rarely involves the jaws.

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16
Q

What are the three grades of chondrosarcoma?

A
  1. Grade I
  2. Grade II
  3. Grade III

The grades correlate with tumor growth rate and prognosis.

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17
Q

What is Ewing’s Sarcoma traditionally regarded as?

A

An undifferentiated type of bone sarcoma of children, linked with primitive neuroectodermal tumor (PNET)

The current term used is Ewing’s Sarcoma/PNET.

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18
Q

What age group is primarily affected by Ewing’s Sarcoma?

A

Patients between 5 and 20 years

Jaw involvement is uncommon.

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19
Q

What are common symptoms of Ewing’s Sarcoma?

A

Pain with swelling

Fever, leukocytosis, and elevated ESR may also be present.

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20
Q

What is the treatment for Ewing’s Sarcoma?

A

High dose radiotherapy and multidrug chemotherapy

This approach has improved the 5-year survival rate to 75%.

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21
Q

What are the characteristics of malignant lymphoma in bone?

A

Can involve the skeletal system primarily or as a manifestation of systemic disease

Large cell lymphoma is more common in adults.

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22
Q

What is Burkitt’s Lymphoma associated with?

A

B-lymphocyte origin that has a predilection to jaws

It is related to Epstein-Barr virus (EBV).

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23
Q

What is the classic histopathological feature of Burkitt’s Lymphoma?

A

Starry sky pattern

This pattern is caused by the presence of histiocytes within the tumor tissue.

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24
Q

What is Multiple Myeloma?

A

A malignancy of plasma cell origin within bone

Accounts for nearly 50% of all malignancies that involve the bone.

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25
Q

What are common clinical features of Multiple Myeloma?

A

Bone pain, pathologic fractures, fatigue, fever, infection, and bleeding tendency

These symptoms are due to abnormal platelet function.

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26
Q

What radiographic feature is characteristic of Multiple Myeloma?

A

Multiple well-defined, punched out radiolucencies

The jaws may be involved in 30% of cases.

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27
Q

What is the median age at diagnosis for the disease described?

A

60-70 years

Rarely diagnosed before the age of 40.

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28
Q

List some clinical features of the disease.

A
  • Bone pain
  • Pathologic fractures
  • Fatigue
  • Fever
  • Infection
  • Bleeding tendency due to abnormal platelet function
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29
Q

What are the radiographic features of the disease?

A
  • Multiple well-defined punched out radiolucencies
  • Ragged radiolucencies
  • May affect the skull and jaws in 30% of cases
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30
Q

What histopathological features are observed in this disease?

A
  • Diffuse, monotonous sheets of neoplastic, variably differentiated, plasmacytoid cells
  • Frequent mitoses
  • Amyloid deposits may be seen
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31
Q

What are the four key diagnostic methods for this disease?

A
  • Skeletal X-ray showing radiolucency
  • Histopathology revealing neoplastic plasma cells
  • Bone-marrow examination showing at least 10% atypical plasma cells
  • Bence-Jones proteins in urine (30-50%)
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32
Q

What is the prognosis and survival rate for this disease?

A

Poor prognosis with a 5-year survival rate of 25%

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33
Q

Define Plasmacytoma.

A

A unifocal, monoclonal, neoplastic proliferation of plasma cells usually arising within bone.

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34
Q

What is the average age at diagnosis for Plasmacytoma?

A

55 years

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35
Q

What are the clinical and radiographic features of Plasmacytoma?

A
  • Affects adult males
  • Most lesions are central within a bone
  • Pain and swelling, but some cases are asymptomatic
  • X-ray shows well-defined unilocular radiolucency
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36
Q

How does Plasmacytoma differ from Multiple Myeloma?

A

All the findings in the diagnosis of Multiple Myeloma are negative in Plasmacytoma.

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37
Q

What is Langerhans Cell Histiocytosis?

A

A spectrum of disorders characterized by proliferation of histiocyte-like cells, accompanied by eosinophils, lymphocytes, plasma cells, and multinucleated giant cells.

38
Q

What are the three clinical and radiographic findings of Langerhans Cell Histiocytosis?

A
  • Monostotic or polyostotic eosinophilic granuloma of bone without visceral involvement
  • Chronic disseminated histiocytosis (Hand-Schüller-Christian disease)
  • Acute disseminated histiocytosis (Letterer-Siwe disease)
39
Q

What are the histopathological features of Langerhans Cell Histiocytosis?

A
  • Diffuse infiltration of large pale-staining mononuclear cells resembling histiocytes
  • Indistinct cytoplasmic borders with rounded or indented vesicular nuclei
  • Varying numbers of eosinophils
40
Q

What is the treatment for maxillary and mandibular lesions in Langerhans Cell Histiocytosis?

A

Curettage

41
Q

What is the most common form of cancer involving bone?

A

Metastatic carcinoma

42
Q

Which cancers commonly metastasize to the jaw?

A
  • Breast carcinoma
  • Lung carcinoma
  • Kidney carcinoma
  • Thyroid carcinoma
  • Prostate carcinoma
43
Q

What are common clinical findings in metastatic tumors to the jaw?

A
  • Pain
  • Lump
  • Loosening of teeth
  • Paresthesia
  • May be asymptomatic
44
Q

What are the radiographic features of metastatic tumors to the jaw?

A
  • May be lytic, resembling a cyst
  • May cause widening of periodontal ligament
  • Can stimulate new bone formation, appearing radiopaque or mixed
45
Q

What is the prognosis for metastatic carcinoma of the jaws?

A

Poor prognosis with most patients not surviving more than 1 year

46
Q

What factors are necessary for establishing a diagnosis of metastatic carcinoma?

A
  • Careful medical history
  • Complete physical examination
  • Appropriate laboratory studies
47
Q

What is the most frequent primary bone malignancy, exclusive of hematopoietic malignancies?

A

Osteosarcoma

Osteosarcoma is particularly common in patients aged 10 to 25 years.

48
Q

What age group is primarily affected by osteosarcoma?

A

Patients between 10 to 25 years of age, with another peak after 40

Osteosarcoma is exceptionally rare in preschool children.

49
Q

What percentage of all osteosarcomas do osteosarcomas of the jaws represent?

A

6-8%

These are most often found in the 3rd to 4th decade of life.

50
Q

What are common symptoms of jaw osteosarcoma?

A

Swelling and pain

Other features may include loosening of teeth, parasthesia, and nasal obstruction.

51
Q

Which regions of long bones are most commonly affected by osteosarcoma?

A

Metaphyseal region, particularly the lower end of the femur, upper end of tibia, and upper end of humerus

Less commonly, they are found in flat bones such as craniofacial bones, pelvis, and scapula.

52
Q

What are the predisposing factors for osteosarcoma?

A
  1. Paget’s disease
  2. Radiation exposure
  3. Chemotherapy
  4. Pre-existing benign bone lesions
  5. Foreign bodies

Examples include fibrous dysplasia and orthopedic implants.

53
Q

What is the mean age for patients with osteosarcoma of the jaw?

A

About 33 years

This is 10 to 15 years older than the mean age for osteosarcomas of the long bones.

54
Q

What radiographic feature is common in jaw osteosarcoma?

A

Classical sunburst or sunray appearance

This appearance is due to osteophytic bone production on the surface of the lesion.

55
Q

What is a key histopathological feature for diagnosing osteosarcoma?

A

Detection of osteoid and calcified osteoid produced by tumor cells

Osteoid is recognized by its eosinophilic-staining quality and glassy appearance.

56
Q

How are osteosarcomas subclassified?

A
  1. Osteoblastic
  2. Chondroblastic
  3. Fibroblastic

These subtypes do not have any prognostic significance.

57
Q

What is the prognosis for osteosarcoma of the jaw compared to those in long bones?

A

Less aggressive and lower grade

Metastases are seen less frequently, with 30-50% survival rates.

58
Q

What is a chondroma?

A

Benign tumors composed of mature hyaline cartilage

Commonly located in short tubular bones of the hands and feet.

59
Q

What is the peak age for the diagnosis of chondromas?

A

3rd to 4th decade of life

They usually present as painless slow-growing lesions.

60
Q

What is the treatment for a diagnosed chondroma in the jaw?

A

Radical resection

Chondromas in the jaw should be considered potential chondrosarcomas.

61
Q

What is a chondrosarcoma?

A

A malignant tumor characterized by the formation of cartilage by tumor cells

Chondrosarcoma rarely involves the jaws.

62
Q

What are the three grades of chondrosarcoma?

A
  1. Grade I
  2. Grade II
  3. Grade III

The grades correlate with tumor growth rate and prognosis.

63
Q

What is Ewing’s Sarcoma traditionally regarded as?

A

An undifferentiated type of bone sarcoma of children, linked with primitive neuroectodermal tumor (PNET)

The current term used is Ewing’s Sarcoma/PNET.

64
Q

What age group is primarily affected by Ewing’s Sarcoma?

A

Patients between 5 and 20 years

Jaw involvement is uncommon.

65
Q

What are common symptoms of Ewing’s Sarcoma?

A

Pain with swelling

Fever, leukocytosis, and elevated ESR may also be present.

66
Q

What is the treatment for Ewing’s Sarcoma?

A

High dose radiotherapy and multidrug chemotherapy

This approach has improved the 5-year survival rate to 75%.

67
Q

What are the characteristics of malignant lymphoma in bone?

A

Can involve the skeletal system primarily or as a manifestation of systemic disease

Large cell lymphoma is more common in adults.

68
Q

What is Burkitt’s Lymphoma associated with?

A

B-lymphocyte origin that has a predilection to jaws

It is related to Epstein-Barr virus (EBV).

69
Q

What is the classic histopathological feature of Burkitt’s Lymphoma?

A

Starry sky pattern

This pattern is caused by the presence of histiocytes within the tumor tissue.

70
Q

What is Multiple Myeloma?

A

A malignancy of plasma cell origin within bone

Accounts for nearly 50% of all malignancies that involve the bone.

71
Q

What are common clinical features of Multiple Myeloma?

A

Bone pain, pathologic fractures, fatigue, fever, infection, and bleeding tendency

These symptoms are due to abnormal platelet function.

72
Q

What radiographic feature is characteristic of Multiple Myeloma?

A

Multiple well-defined, punched out radiolucencies

The jaws may be involved in 30% of cases.

73
Q

What is the median age at diagnosis for the disease described?

A

60-70 years

Rarely diagnosed before the age of 40.

74
Q

List some clinical features of the disease.

A
  • Bone pain
  • Pathologic fractures
  • Fatigue
  • Fever
  • Infection
  • Bleeding tendency due to abnormal platelet function
75
Q

What are the radiographic features of the disease?

A
  • Multiple well-defined punched out radiolucencies
  • Ragged radiolucencies
  • May affect the skull and jaws in 30% of cases
76
Q

What histopathological features are observed in this disease?

A
  • Diffuse, monotonous sheets of neoplastic, variably differentiated, plasmacytoid cells
  • Frequent mitoses
  • Amyloid deposits may be seen
77
Q

What are the four key diagnostic methods for this disease?

A
  • Skeletal X-ray showing radiolucency
  • Histopathology revealing neoplastic plasma cells
  • Bone-marrow examination showing at least 10% atypical plasma cells
  • Bence-Jones proteins in urine (30-50%)
78
Q

What is the prognosis and survival rate for this disease?

A

Poor prognosis with a 5-year survival rate of 25%

79
Q

Define Plasmacytoma.

A

A unifocal, monoclonal, neoplastic proliferation of plasma cells usually arising within bone.

80
Q

What is the average age at diagnosis for Plasmacytoma?

A

55 years

81
Q

What are the clinical and radiographic features of Plasmacytoma?

A
  • Affects adult males
  • Most lesions are central within a bone
  • Pain and swelling, but some cases are asymptomatic
  • X-ray shows well-defined unilocular radiolucency
82
Q

How does Plasmacytoma differ from Multiple Myeloma?

A

All the findings in the diagnosis of Multiple Myeloma are negative in Plasmacytoma.

83
Q

What is Langerhans Cell Histiocytosis?

A

A spectrum of disorders characterized by proliferation of histiocyte-like cells, accompanied by eosinophils, lymphocytes, plasma cells, and multinucleated giant cells.

84
Q

What are the three clinical and radiographic findings of Langerhans Cell Histiocytosis?

A
  • Monostotic or polyostotic eosinophilic granuloma of bone without visceral involvement
  • Chronic disseminated histiocytosis (Hand-Schüller-Christian disease)
  • Acute disseminated histiocytosis (Letterer-Siwe disease)
85
Q

What are the histopathological features of Langerhans Cell Histiocytosis?

A
  • Diffuse infiltration of large pale-staining mononuclear cells resembling histiocytes
  • Indistinct cytoplasmic borders with rounded or indented vesicular nuclei
  • Varying numbers of eosinophils
86
Q

What is the treatment for maxillary and mandibular lesions in Langerhans Cell Histiocytosis?

A

Curettage

87
Q

What is the most common form of cancer involving bone?

A

Metastatic carcinoma

88
Q

Which cancers commonly metastasize to the jaw?

A
  • Breast carcinoma
  • Lung carcinoma
  • Kidney carcinoma
  • Thyroid carcinoma
  • Prostate carcinoma
89
Q

What are common clinical findings in metastatic tumors to the jaw?

A
  • Pain
  • Lump
  • Loosening of teeth
  • Paresthesia
  • May be asymptomatic
90
Q

What are the radiographic features of metastatic tumors to the jaw?

A
  • May be lytic, resembling a cyst
  • May cause widening of periodontal ligament
  • Can stimulate new bone formation, appearing radiopaque or mixed
91
Q

What is the prognosis for metastatic carcinoma of the jaws?

A

Poor prognosis with most patients not surviving more than 1 year

92
Q

What factors are necessary for establishing a diagnosis of metastatic carcinoma?

A
  • Careful medical history
  • Complete physical examination
  • Appropriate laboratory studies