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Information

 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: 7–25 years (range, 19 months–56 years); 2nd + 3rd decade (73%); 5–25 years (90%); uncommon <5 and >40 years of age; uncommon in Blacks; M÷F = 2÷1 to 3÷1

Location:

  1. 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
  2. spine (10–14%): 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
  3. skull, scapula, rib, pelvis, mandible, patella

Radiographically difficult areas: vertebral column, femoral neck, small bones of hand + feet

NUC (bone scintigraphy is the most sensitive method!):

CT (for characterization + precise localization of nidus):

MR (diminished conspicuity of lesion compared with CT):

Angio:

Prognosis: no growth progression, infrequently regression

Rx:

  1. complete surgical excision of nidus (reactive bone regresses subsequently)
  2. percutaneous CT-guided removal
  3. percutaneous ablation with radio-frequency electrode / laser / alcohol

DDx:

  1. Stress fracture (focal cortical ridge, decreasing size, linear intense uptake of bone tracer)
  2. Intracortical abscess (irregular inner margin, eccentric sequestrum, no central enhancement)
  3. Intracortical hemangioma (vertically aligned intralesional calcifications, hyperintense lesion with hypointense septa)
  4. Small chondroblastoma (epiphyseal intramedullary location, punctate calcification)
  5. Osteoblastoma (less painful, no response to salicylate, more expansile + larger than 2 cm, progressive growth)
  6. Compensatory hypertrophy of pedicle (contralateral spondylolysis, lack of nidus)

Intracortical Osteoid Osteoma (most common)  !!navigator!!

= 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)  !!navigator!!

= intramedullary

Intraarticular lesion difficult to identify with delay in diagnosis of 4 months–5 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)  !!navigator!!

= 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)  !!navigator!!

= 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