2.7 Bone Tumor Pathology Flashcards

1
Q

osteosarcoma is a malignant proliferation of __________

A

osteoblasts

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2
Q

Peak incidence of osteosarcoma is in what age group?

A

teenagers, less commonly seen in elderly

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3
Q
  • Risk factors for this bone tumor are familial retinoblastoma, Paget disease, and radiation exposure
  • commonly in metaphysis of the knee, malignant cells make osteoid
A

osteosarcoma

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4
Q

This bone tumor arises in the metaphysis of long bones, usually the distal femur or proximal tibia, and presents as a pathologic fracture or bone pain with swelling

A

osteosarcoma

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5
Q

imaging of this bone tumor reveals a destructive mass with a “sunburst” appearance and lifting of the periosteum

A

osteosarcoma

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6
Q

malignant hyaline and mixoid cartilage forming tumor that arises in medulla of pelvis or central skeleton (pelvis, shoulder, ribs), typically 40 years or older

A

chondrosarcoma

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7
Q

Ewing sarcoma is a malignant proliferation of poorly-differentiated cells derived from _____________

A

neuroectoderm

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8
Q

This bone tumor arises in the diaphysis of long bones, usually in male children less than 15 years of age, 2nd mot common bone tumor in children

A

Ewing Sarcoma

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9
Q

Biopsy of this bone tumor reveals small, round blue cells that resemble lymphocytes (can be confused with lymphoma or chronic osteomyelitis), 11;22 translocation is characteristic

A

Ewing sarcoma

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10
Q

more common than primary tumors, usually result in osteolytic (punched out) lesions, prostatic carcinoma classically produces osteoblastic lesions

A

metastatic tumors

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11
Q
  • pancytopenia, proteinuria, lytic lesion in skull and spine, excess IgGk
  • osteoblast inhibition, releases IL-1, activates osteoclasts
  • lots of plasma cells on histo
  • blacks, 50-60 yo
A

multiple myeloma (plasmacytoma if singular)

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12
Q

-presents with fever/chills, common in children, responds to chemo
-small round blue cells on histo
(11;22) translocation

A

Ewing’s Sarcoma

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