BONE LESIONS
NORMAL SPINAL BONE MARROW
APPROACH
AGGRESSIVE APPEARANCE
Indistinct margins
Wide zone of transition
Aggressive periosteal reaction
Permeative appearance
ST component
Endosteal scalloping
NONAGGRESSIVE APPEARANCE
Sclerotic margins
Narrow zone of transition
Well-circumscribed
No endosteal scalloping, aggressive periosteal reaction or ST component
Think of bone lesions in 4 groups:
Aggressive features
IDK what it is (aggressive but nonspecific features)
Very common in clinical practice; ddx by age.
Adult: mets/myeloma
Children: ewing/infection
I know what it is! (lesion w/ characteristic imaging features)
Very rare in clinical practice: osteosarcoma, chondrosarcoma.
Nonaggressive features
IDK what it is (nonaggressive but nonspecific features)
Very common in clinical practice; can say fibro-osseous lesion to sound smart.
I know what it is! (characteristic imaging features)
Enchondroma, osteoid osteoma, non-ossifying fibroma, hemangioma, giant cell tumor, fibrous dysplasia.
LUCENT LESIONS OF BONE
SCLEROTIC LESIONS OF BONE
BONE FORMING LESIONS
ENOSTOSIS (BONE ISLAND)
RADIOGRAPH
Homogeneously dense, fading at periphery and merging into normal marrow.
Periphery brush-like; spicules blend w trabeculae
No cortex destruction
CT
Sclerotic lesion follows xray appearance
Peripheral extensions into normal adjacent bone (brush border)
MRI
Low SI on all sequences; faintly higher SI than surrounding bone w fat suppression
Spicules aligned w trabeculae
No enhancement w contrast.
Benign focus of compact (cortical) bone located w/n cancellous bone (medullary cavity); small spiculated osteoblastic focus
Location: can be found in any bone; pelvis, long bones (epiphyses, metaphysis), ribs, spine most frequent
Size: usually small <1 cm; may be giant >2 cm (most difficult to differentiate)
Morphology: round, oval, oriented along long axis of bone.
Can be multiple in some bone or polyostotic; if multiple and concentrated in metaphyses and epiphyses = osteopoikilosis
Osteopoikilosis: AD syndrome of multiple bone islands and keloid formation.
Clinically significance: must differentiate from an osteoblastic mets, osteoid osteoma or a low-grade osteosarcoma.
Bone scan: usually normal
Osteopathia striata: benign asx sclerotic dysplasia characterized by linear bands of sclerosis in the long bones and fan-like sclerosis in the flat pelvic bones.
DDX
Sclerotic mets: can have identical appearance; may not be as homogeneous dense throughout.
Mets generally show some enhancement on MR.
Positive PET/CT is helpful; Not exclusionary is lesion is small or underlying suspected mets is not typically FDG-avid (adenoid cystic CA, medullary thryoid, myxoid liposarcoma)
Nonossifying fibroma
Typically not as dense; Generally heal during teenage years w slightly sclerotic bone forming periphery -> eventually replaced by normal bone or leave faint trace of homogeneous sclerosis;
Cortical rather than medullary.
Osteoma
Dense focus; usual location is paranasal sinus or skull. If located peripherally, arises on outer cortex of bone, not w/n marrow. Generally homogeneously sclerotic, though may have regions of inhomogeneity.
Osteoid osteoma:
Usually have lytic nidus +/- central sclerotic focus
Nidus may be obscured on radiograph by homogenous sclerotic bone rxn.
Lytic nidus always evident wither w CT or MR; extensive regional edema on MR.