Tumours Flashcards

1
Q

Osteoma (Gardner’s Syndrome)

A

Benign Sclerotic Tumour

  • Asymotomatic
  • Female 3:1
  • Frontal or ethmoid sinus distribution
  • Round/oval radiopaque, mostly <2cm
  • Small, white, solid, osseous growths off the outer cortex of bone
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2
Q

Osteoid Osteoma

A

Benign Sclerotic Tumour

  • 10-15 years
  • Male 2:1
  • Proxima Femur, Tibia, Lumbar Spine (pedicle)
  • Lucent nidus <1cm (nidus = vascularised fibrous connective tissue)
  • Relieved by asprin
  • Reactive sclerosis, cortical thickening, solid periosteal reaction
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3
Q

Brodie’s Abscess

A

Benign Lucent Tumour

  • Lesion is close to growth plates
  • Lucency greater than 1 cm
  • Drainage tract toward the epiphysis
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4
Q

Bone Island (Enostoma)

A

Benign Sclerotic Tumour

  • Ischium, Illium, Sacrum, Proximal femur
  • Not in the skull
  • Intramedullary location
  • Adults
  • Round, Radiopaque lesions
  • long axis of bone
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5
Q

Osteochondroma

A

Benign

  • Most common skeletal tumour
  • 75% discovered before age 20
  • Femur, TIbia, Humerus
  • Exostosis = grows form the cortex of bone
  • Peduculated, Sessile, Cauliflower presentation
  • The lesions begin as growth of new bone off the cortex of long bones and then cartliage is calcified within the lesion giving a slcerotic and lucent appearance
  • These are usually asymptomatic unless obstrucitng internal strucutres
  • Multiple Osteochondroma’s = Heriditory Multiple Exostosis
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6
Q

Enchondroma

A

Lucent Benign Tumour

  • Most common tumour of the hand
  • 50% have a calcification of the cartilage in the matrix
  • Can progress in to malignant chondrosarcoma
  • Lytic, geograpgic lesion occuring in the metaphysis
  • Mildly expansive with endosteal scalloping
  • Stippled calcification in the matrix
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7
Q

Haemangioma

A

Benigns Lucent Tumour

  • Female
  • >40 years
  • Most common tumour of the spine
  • Thoracolumbar vertebral body, Skull
  • Vertical striations in the vertebral body

DDx.

  • Padget’s
  • Osteoporosis
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8
Q

Fibrous Xanthoma

A

Lucent Benign

  • Fibrocortical defect
    • 4-8 years <2cm
    • Male 2:1
    • Posterior medial surface of distal femour most common
  • Nonossifying fibroma
    • 8-20 years 2-7cm
    • Males 2:1
    • Distal tibia, dital femur, proximal tibia, humerus, fibula
  • Diametaphyseal
  • Eccentric, oval lytic lesion with well defined rim of scleorsis
  • Thinned cortex
  • Soap bubble appearance
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9
Q

Simple Bone Cyst

A

Benign Lucent

  • Fluid filled cyst lined with fibrous tissue
  • 3-14 years of age
  • Proximal humerus, Proximal femur
  • Truncated lesion starting in the metaphysis and tapering into the diaphysis. It does not cross into the epiphysis
  • Soap bubble matrix
  • mild endosteal scollaping
  • No periosteal reaction
  • Fallen fragment sign or hinge fragement sign if fragment isnt completly detached
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10
Q

Aneurysmal Bone Cyst

A

Benign Lucent

  • Non-neoplastic blood folled cavity
  • Female 3:2
  • 5-20 years
  • Long bones and thoracolumbar spine
  • Metaphyseal and diaphyseal
  • Rapidly expanding reaching 8-10cm in diameter
  • Egg shell rim of sclerosis
  • Buttressing of new periosteal bone
  • Will no extend into epiphysis of gorwht plate is closed
  • Exapansion into vertebral body is knwn as balloon in finger sign
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11
Q

Giant Cell Tumour

A

Lucent Benign

  • Quasimalignant tumour
  • Also known as osteoclastomas
  • 5-20% of malignant
  • Malignant tumour
    • Male 2:1
  • Benign
    • Female 3:2
  • 20-40 years of age after clsure of epiphysis
  • Distal femur, proximal tibia, proximal humerus, distal radius
  • Distal radius is 99% malignant
  • Most common benign tumour of saccrum
  • Metaphyseal that can extend into epiphysis
  • Eccentric, lytic, geographic, soap bubble matrix, expansive lesion, thinning of cortex
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12
Q

Osteosarcoma

A

Malignant Sclerotic

  • Abnoormal osteoblastic cells
  • 5 types
    • Central (conventional)
    • Multicentric
    • Parosteal (juxtacortical)
    • Extraosseous
    • Secondary
  • Males 2:1
  • 10-20 years
  • 50% osseous neoplastic lesion (sclerotic), 25% comprised of connective tissue (lytic), 25% are a mixed lesion
  • Occur around the knee in the metaphysis
  • Metastases to lungs, bones kidneys
  • Dense ivory sclerosis filling meduallry cavity, or permitive lytic lesion, poorly defined zone of transition
  • Cortical disruption, Aggressive periosteal reaction, bone exapnsion
  • Roughened lobulated boarder (cumulus cloud)
  • Large soft tissue mass may also ossify
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13
Q

Multiple Myeloma

A

Malignant Lucent

  • Malignant proliferation of plasma cells that replace bone marrow
  • Most common malignnant tumour
  • Male 2:1
  • Thoracolumbar junction most common
  • Diaphysis of long bones (rarelt bellow the knee and elbow)
  • Hallmark sign: Osteolytic defects
    • sharply circumscribed
    • punched out lesions
    • skull, pelvis, long bones, clavicle, ribs
    • raindrop skull
    • uniform size differentiates from lytic metasteses
    • endosteal scalloping
  • Diffuse osteolytic round/ocal lesions without reactive sclerosis in diaphysis with endosteal scalloping
  • Diffuse, unexplained osteoporosis in vertebral bodies
  • Wrinkles vertebra sign may be single or multiple

DDx

  • Ewing’s sarcoma, Non-hodgkin’s lymphoma,
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14
Q

Ewings Sarcoma

A

Malignnat Lucent

  • Males 2:1
  • Proliferationof primitive round cells
  • Long bones are more affected in younger patients
    • femur, tibia, humerus
  • Flat bones more affected in older patients
    • pelvis, ribs
  • Most common tumour to metasesise to lungs and and bone
  • Diaphyseal apressive lucent lesion
  • Permative with wide xone of transition
  • Periosteal raction = sunburst and codmans triangle
  • Cortical saucerisation (shallow concave defect on outer cortex)

DDx

  • Osteosarcoma
  • Osteomyelitis
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15
Q

Non-Hodgkin’s Lymphoma

A

Malignant Lucent

  • Reticulum cell sarcoma
  • Round cell tumour
  • Adults 50-80 years
  • Males 2:1
  • Femur, tibia, humerus diaphysis
  • Pelvis, ribs, scapula, vertebrae
  • Permative, moth eaten appearence in medullary cavity
  • Patch destruction of cortex
  • Minimal periosteal reaction, with soft tissue mass
  • Vertebral collapse
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16
Q

Chondrosarrcoma

A

Malignant Lucent

  • Malignant chondrogenic producing cartilage and callagen which often calcifies
  • Males 2:1
  • Pelvis, femur, humerus
  • Most common tumour of hand, sternum, scapula
  • large radiolucent lesion wit poorly defined margins
  • Expansion/enlargement of bone
  • Metaphysis/Diaphysis
  • Endosteal scalloping, cortical thinning
  • Circular radiolucent giving bubble appearence in matrix
  • 2/3 of lesion with a cotton woll appearance (foci of calcification)
  • Cortical destruction
17
Q

Fibrosarcoma

A

Malginant Lucent

  • 30-50 years
  • Female = Male
  • Produces varying amounts of malignant fibrous collagen
  • 50% occur around the knee
  • Eccentric lytic lesion, cortical thinning and endosteal erosion
  • permative destruction, wide zone of transition
  • Often produces hyge soft tissue mass
18
Q

Metasteses

A

Osteolytic

  • Cortical and trabecular destruction
  • Lack of bone expansion
  • Lack of periosteal response
  • Moth-eaten, permative destruction
  • Small or absent soft tissue mass

Osteoblastic metasteses

  • Localised or diffuse increased bone density
  • poorly defined margins

Mixed metasteses

  • Combination of features