Bone tumors and tumor-like lesions

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27 Terms

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Bone tumors and tumor-like lesions (3)

  1. Osteosarcoma

  2. Chondrosarcoma

  3. Ewing Sarcoma

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Osteosarcoma Pathogenesis

Tumor fills the bone and forms a soft tissue mass on both sides of the bone

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What bones does Osteosarcoma Typically Take Place (3)

  1. Proximal tibia

  2. Distal femur

  3. Proximal humorous

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Osteosarcoma Mutations (2)

RB, TP53

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Osteosarcoma Histology (2)(1)

  • Primitive trabeculae (Osteoid or Immature bone)

    • Thought to arise from primitive bone-forming cells

  • Hyperchromatic nuclei

<ul><li><p>Primitive trabeculae (Osteoid or Immature bone)</p><ul><li><p>Thought to arise from primitive bone-forming cells</p></li></ul></li><li><p>Hyperchromatic nuclei</p></li></ul><p></p>
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Osteosarcoma Clinical presentation (4)

  1. Chronic bone pain

  2. May be palpable mass

  3. Soft tissue extension

  4. More radio dense

<ol><li><p>Chronic bone pain</p></li><li><p>May be palpable mass</p></li><li><p>Soft tissue extension</p></li><li><p> More radio dense</p></li></ol><p></p>
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Osteosarcoma Another radiologic feature

Codman triangle

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How does the Codman Triangle Occur (2)

  1. Periosteum lifted off

  2. Periosteal reaction (rim of reactive new subperiosteal bone)

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Chondrosarcoma Commonality

Most common = “conventional type” 90%

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Chondrosarcoma Produces

hyaline cartilage

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Chondrosarcoma Age

greater than 40

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Chondrosarcoma Location

axial skeleton (pelvis, ribs, shoulders)

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Chondrosarcoma can be secondary to

secondary to preexisting enchondroma or osteochondroma

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Chondrosarcoma Tumor Grade and Prognosis (3)

  • Vary from low grade →

  • Slow growing to high grade with high metastatic potential

  • Poor prognosis

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Chondrosarcoma Symptoms

  • Local swelling and pain

  • Pathologic fracture as tumor grows

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Ewing Sarcoma Age

80% are younger than 20

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Ewing Sarcoma Origin

Cell of origin not known. May be mesenchymal stem cells or primitive neuroectodermal cells

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Ewing Sarcoma Bones of Origin (2)

  • Most often in diaphysis of long bones and bones of the pelvis

  • 20% are extraskeletal

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Ewing sarcoma Genetic Mutation (3)

  • Translocation between chromosomes 11 and 22

  • FLI1 gene

  • EWSR1 gene

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Ewing Sarcoma Gross morphology

Irregular tumor mass breaking through the bone cortex

<p>Irregular tumor mass breaking through the bone cortex</p>
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<p>Ewing Sarcoma Radiology</p>

Ewing Sarcoma Radiology

knowt flashcard image
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Ewing Sarcoma Histology

  • Sheets of small, round cells

  • Hyperchromatic nuclei

  • Little cytoplasm

<ul><li><p> Sheets of small, round cells</p></li><li><p>Hyperchromatic nuclei</p></li><li><p>Little cytoplasm</p></li></ul><p></p>
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<p>Ewing Sarcoma Histology - This is a tumor that was isolated from bone.  What type of tissue is missing?</p>

Ewing Sarcoma Histology - This is a tumor that was isolated from bone. What type of tissue is missing?

No bone and cartilage

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Ewing Sarcoma Symptoms

  • Painful large masses

  • Tender, warm, swollen

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Osteosarcoma Summary (3)

  • Bony Growth

  • Periosteal Reaction

  • Long bones, near joints

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Chondrosarcoma Summary (2)

  • Cartilaginous Growth (Hyaline)

  • Axial Skeleton

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Ewing Sarcoma Summary (5)

  • Unknown origin

  • Irregular tumor breaks through cortex

  • Long bones and pelvis

  • Periosteal Reaction

  • Genetic component