Part 6: Bone Tumours

 

BENIGN BONE TUMOURS

  • Well defined, often sclerotic, margin
  • Expansile lesion may result in cortical thinning but no cortical destruction
  • A periosteal reaction may be present which appears uniform and solid

 

Enchondroma

  • Benign cartilaginous tumour
  • Typically found in the diaphyses of the metatarsals and phalanges
  • Well defined, radiolucent and mildly expansile with cortical thinning
  • May have internal calcification
  • Multiple enchondromas (as seen in Ollier’s disease) may have malignant potential

Multiple enchondromas (arrows) in Ollier’s disease

 

Osteochondroma

  • Cartilage-capped exostosis seen as a bony outgrowth
  • Cartilaginous component invisible on plain radiographs unless calcified
  • Rarely, the cartilage cap may undergo transformation to malignant chondrosarcoma; cartilage cap thickness > 2cm is suspicious and usually assessed on MRI
  • Pedunculated, subungual exostoses on the distal phalanx of the hallux are common and usually have a cartilaginous cap, classifying them as osteochondromata

Osteochondroma of first proximal phalanx (arrow)

 

Intraosseous lipoma

  • Typically occurs in the calcaneum
  • Well-defined lucent lesion; may contain central calcification
  • MRI diagnostic to confirm fatty matrix, seen as high T1 and T2 signal which supresses with fat saturation

Intraosseous lipoma calcaneum

 

Fibrous cortical defect

  • Common, up to 20 % of immature skeletons
  • Caused by fibrous tissue from the periosteum invading the underlying cortex; may be related to a subclinical injury
  • Usually an incidental finding
  • Seen as a cortically-based, radiolucent lesion with well-defined sclerotic border in the tibial metaphyses
  • Larger lesions (>2cm) that expand into the medullary cavity are referred to as non-ossifying fibromas

Fibrous cortical defect with well-defined sclerotic margin

 

Solitary (simple) bone cyst

  • Cyst of unknown origin containing clear or serosanguinous fluid
  • Occurs in the immature skeleton
  • May occur in distal tibia / fibula, calcaneum and long bones of the foot
  • Seen as a well-demarcated, radiolucent intramedullary lesion with cortical thinning
  • May present with a pathological fracture

Simple bone cyst distal fibula seen as well-defined, slightly expansile lucent lesion

 

Aneurysmal bone cyst

  • Usually in patients <30 years
  • Sponge-like cyst with blood-filled spaces and fibrous septae; may arise as the result of a vascular anomaly
  • Seen as radiolucent, often rapidly expansile lesion with a thin cortical shell
  • Matrix fluid-fluid levels on MRI are typical

Aneurysmal bone cyst with fluid-fluid levels on MRI

 

Osteoid osteoma

  • Typically in young patients who complain of severe rest and night pain
  • Dramatic relief with aspirin
  • Seen as ovoid radiolucent nidus up to 1cm in diameter surrounded by sclerosis and periosteal thickening
  • Sclerosis may mask the radiolucent nidus on plain radiographs; best seen on thin CT sections

Osteoid osteoma with radiolucent nidus (arrows) and surrounding sclerosis best seen on CT

 

Giant cell tumour of bone

  • Occur primarily in the mature skeleton
  • Typical eccentric epiphyseal location, extending to subarticular surface
  • Seen as radiolucent lesion with well-defined, but non-sclerotic, margin
  • May be expansile with cortical thinning
  • Approximately 15% of giant cell tumours are malignant

Giant cell tumour of distal tibia seen as eccentric expansile epiphyseal lucent lesion (arrows)

 

MALIGNANT BONE TUMOURS

 

  • Ill-defined margin
  • Permeative, ‘moth-eaten’ appearance
  • Cortical destruction
  • Periosteal reaction has lamellated (‘onion-skinned’) or spiculated (‘hair on end’ or ‘sunray’) appearance
  • Soft tissue mass: distortion of adjacent soft tissue contour with increased density; may have calcification

 

Osteosarcoma

  • Uncommon in the foot
  • Typically occurs in immature skeleton; may occur in older age group usually secondary to Paget’s
  • Seen as ill-defined, often mixed lytic and sclerotic lesion
  • As tumour osteoid becomes mineralized, there is increasing sclerosis and new bone formation with a ‘cloud-like’ density
  • Aggressive periosteal reaction with wedge of ossified tissue under the periosteum called a Codman’s triangle

Osteosarcoma calcaneus with sclerosis on xray (left) and low signal on MRI (right) due to osteoid formation

 

Ewing’s sarcoma

  • Occur in immature skeleton
  • Seen as an ill-defined, permeative lesion in diaphysis of a long bone or within a flat bone
  • Often has cortical destruction and spiculated periosteal reaction
  • Osteomyelitis has a similar radiographic appearance

Ewing’s sarcoma with ill-defined, permeative infiltration of fibula (arrows) and cortical destruction (arrowheads)

 

Chondrosarcoma

  • Cartilaginous tumours are rare in the foot but have been noted in the calcaneum
  • Occur in the mature skeleton ~50-70y
  • Usually contain calcification which has a ‘popcorn’ or ‘snowflake’ appearance indicative of their cartilaginous origin

Chondrosarcoma posterior distal tibia with ‘popcorn-like’ chondroid calcification (arrows)

 

Metastases

  • Needs to be considered in the differential diagnosis of any lytic lesion in a patient >40 years
  • Metastases to the foot are most commonly from primary lung carcinoma
  • Usually lytic, destructive lesions
  • Sclerotic lesions most commonly prostate and breast metastases
  • Thyroid and renal metastases produce expansile lesions

Metastasis base 5th metatarsal seen as lytic destructive lesion (arrow) in patient with known lung carcinoma