Bone and Soft-Tissue Disorders
= benign osteoblastic neoplasm characterized by intracortical nidus of osteoid tissue / woven mineralized immature bone, often surrounded by dense sclerotic reactive bone
Size:<1.5 cm in diameter (per definition);
N.B.: lesion >1.5 cm = osteoblastoma
Frequency: 12% of benign bone tumors
Etiology: ? inflammatory response
Histo: small nidus of osteoid-laden interconnected trabeculae with background of highly vascularized fibrous connective tissue surrounded by zone of reactive bone sclerosis; osteoblastic rimming; indistinguishable from osteoblastoma [nidus, Latin = nest]
Mean age: 725 years (range, 19 months56 years); 2nd + 3rd decade (73%); 525 years (90%); uncommon <5 and >40 years of age; uncommon in Blacks; M÷F = 2÷1 to 3÷1
- tender to touch + pressure
- local pain (9598%), weeks to years in duration, worse at night, decreased by activity:
- salicylates give relief in 2030 minutes in 7590%
- prostaglandin E2 elevated 1001000 x normal within nidus (probable cause of pain and vasodilatation)
Location:
- meta- / diaphysis of long bones (73%): upper end of femur (43%), hands (8%), feet (4%); frequent in proximal tibia + femoral neck, fibula, humerus; no bone exempt
- spine (1014%): predominantly in neural arch (50% in pedicle + lamina + spinous process); 20% in articular process) of lumbar (59%), cervical (27%), thoracic (12%), sacral (2%) segments
- painful scoliosis, focal / radicular pain
- gait disturbance, limb atrophy
- skull, scapula, rib, pelvis, mandible, patella
- round / oval radiolucent nidus (75%) of <1.5 cm in size
- variable surrounding sclerosis ± central calcification
- painful scoliosis concave toward lesion / kyphoscoliosis / hyperlordosis / torticollis with spinal location ← spasm
- may show extensive synovitis + effusion + premature loss of cartilage with intraarticular site (lymphofollicular synovitis)
- osteoarthritis (50%) with intraarticular site 1.522 years after onset of symptomatology
- regional osteoporosis ← probably disuse
◊Radiographically difficult areas: vertebral column, femoral neck, small bones of hand + feet
NUC (bone scintigraphy is the most sensitive method!):
- intensely increased radiotracer uptake (increased blood flow + new-bone formation)
- double density sign = small area of focal activity (nidus) superimposed on larger area of increased tracer uptake
CT (for characterization + precise localization of nidus):
- small well-defined round / oval nidus of low attenuation:
- surrounded by variable amount of sclerosis
- nidus with variable amount of mineralization (50%): punctate / amorphous / ringlike / dense
- nidus enhances on dynamic scan
MR (diminished conspicuity of lesion compared with CT):
- heterogeneous nidus ← depending on tumor vascularity and presence of calcifications:
- mostly hypo- to isointense to muscle on T1WI
- variable signal intensity on T2WI; SI may increase to between that of muscle + fat / remains low on T2WI
- perinidal edema / inflammation in adjacent bone marrow + soft tissues (47%)
- synovitis + joint effusion with intraarticular site
Angio:
- highly vascularized nidus with intense circumscribed blush appearing in early arterial phase + persisting late into venous phase
Prognosis: no growth progression, infrequently regression
Rx:
- complete surgical excision of nidus (reactive bone regresses subsequently)
- percutaneous CT-guided removal
- percutaneous ablation with radio-frequency electrode / laser / alcohol
DDx:
- Stress fracture (focal cortical ridge, decreasing size, linear intense uptake of bone tracer)
- Intracortical abscess (irregular inner margin, eccentric sequestrum, no central enhancement)
- Intracortical hemangioma (vertically aligned intralesional calcifications, hyperintense lesion with hypointense septa)
- Small chondroblastoma (epiphyseal intramedullary location, punctate calcification)
- Osteoblastoma (less painful, no response to salicylate, more expansile + larger than 2 cm, progressive growth)
- Compensatory hypertrophy of pedicle (contralateral spondylolysis, lack of nidus)
Intracortical Osteoid Osteoma (most common)
= nidus within cortex accompanied by cortical thickening + reactive sclerosis
Location: shaft of long bone
- solid / laminated periosteal reaction
- fusiform sclerotic cortical thickening
- round / oval radiolucent area <2 cm in diameter within center of osteosclerosis
DDx: Brodie abscess, sclerosing osteomyelitis, syphilis, bone island, stress fracture, osteosarcoma, Ewing sarcoma, osteoblastic metastasis, lymphoma, subperiosteal aneurysmal bone cyst, osteoblastoma
Cancellous Osteoid Osteoma (intermediate frequency)
= intramedullary
◊Intraarticular lesion difficult to identify with delay in diagnosis of 4 months5 years!
Site: juxta- / intraarticular at femoral neck, vertebral posterior elements, small bones of hands + feet
- little osteosclerosis / sclerotic cortex distant to nidus ← functional difference of intraarticular periosteum
- joint space widened ← effusion, synovitis
Subperiosteal Osteoid Osteoma (rare)
= round soft-tissue mass adjacent to bone
Site: juxta- / intraarticular at medial aspect of femoral neck, hands, feet (neck of talus)
- juxtacortical mass excavating the cortex with almost no reactive sclerosis ← bony pressure atrophy
Intraarticular Osteoid Osteoma (rare)
= nidus within / near a joint
Location: hip
- joint tenderness, not necessarily worse at night
- prominent joint effusion ± synovial hypertrophy
- minimal / absent reactive cortical thickening ← lack of cambium (= inner layer of periosteum)
DDx: inflammatory / septic / tuberculous / rheumatoid arthritis, nonspecific synovitis / Legg-Calvé-Perthes disease
Outline