section name header

Information

 Bone and Soft-Tissue Disorders

Pathogenesis: vascular compromise with obliterative endarteritis + periarteritis hypovascularity + hypoxia damage to osteoblasts + osteoclasts hypocellularity + fibrosis decreased matrix production (growing bone + periosteal new bone most sensitive)

Dose effects:

depend on age of patient, absorbed dose, size of radiation field, beam energy, fractionation

>300 rad:microscopic changes
>400 rad:growth retardation
<600–1200 rad:histological recovery retained
>1200 rad:pronounced cellular damage to chondrocytes; bone marrow atrophy + cartilage degeneration after >6 months; vascular fibrosis
  1. FOCAL MARROW DEPLETION
    Pathophysiology: marrow edema, vascular congestion, suppressed hematopoiesis; replacement of marrow elements by fibrosis + fat (complete by 3 months)
    • homogeneous high-intensity signal within radiation port on T1WI
    • occasionally bandlike appearance characterized by peripheral zone of low SI (red marrow) and a central zone of high SI (fatty marrow) on T1WI
  2. BONE GROWTH DISTURBANCE
    • Appendicular skeleton
      • joint space widening cartilage hypertrophy (after 8–10 months)
      • growth plate widening in 1–2 months, often returning to normal by 6 months
      • permanent alteration in bone length / size premature fusion of physis
      • metaphyseal bowing
      • sclerotic metaphyseal bands
      • metaphyseal irregularity + fraying resembling rickets
      • longitudinal striations
      • overtubulation (= abnormal narrowing of the diaphyseal shaft)

      Cx: slippage of femoral / humeral epiphysis ± ischemic necrosis (after doses of >25 Gy)
    • Axial skeleton (dose of <15 Gy)
      • “bone-within-bone” appearance after 9–12 months
      • irreversible scalloping + irregularity of vertebral endplate with decreased height of vertebra (= failure of vertical growth)
      • scoliosis concave toward side of irradiation asymmetric vertebral growth + muscular fibrosis
      • hypoplasia of ilium + ribs
      • acetabular dysplasia, coxa vara / valga
  3. RADIATION OSTEITIS = OSTEORADIONECROSIS = RADIATION NECROSIS
    = bone mottling due to osteopenia + coarse trabeculation and focally increased bone density attempts of osseous repair with deposition of new bone on ischemic trabeculae
    Dose:>6,000 cGy in adults; >2,000 cGy in children
    Time of onset: 1–3 years following radiation therapy
    Location: mandible, ribs, clavicle, humerus, spine, pelvis, femur
    • focal lytic area with abnormal bone matrix:
    • radiolucency confined to radiation field with narrow zone of transition
    • periostitis
    • increased fragility with sclerosis (= pathologic insufficiency fracture)
    • ± cortical thinning from chronic infection

    MR:
    • increased intensity of spinal bone marrow on T1WI + T2WI corresponding to radiation port (fatty infiltration)

    NUC:
    • bone scan with decreased uptake in radiation field

    Cx: increased susceptibility of irradiated bone to infection
    DDx: recurrent malignancy, radiation-induced sarcoma (soft-tissue mass), infection
  4. BENIGN NEOPLASM
    Most likely in patients <2 years of age at treatment; with doses of 1600–6425 rads
    Latent period: 1.5–5–14 years
    1. Osteochondroma = exostosis (exclusively in children under 2 years of age during treatment)
    2. Osteoblastoma
  5. MALIGNANT NEOPLASM
    = RADIATION-INDUCED SARCOMA
    Latency period: 3–55 (average of 11–14) years
    Minimum dose: 1,660–3,000 rad
    Criteria:
    1. malignancy occurring within irradiated field
    2. latency period of >5 years
    3. histologic proof of sarcoma
    4. microscopic evidence of altered histology of the original lesion

    Histo:
    1. Osteosarcoma (90%) = 4–11% of all osteogenic sarcomas
    2. Fibrosarcoma >chondrosarcoma >malignant fibrous histiocytoma
    • pain, soft-tissue mass, rapid progression of lesion