Dr James Wittig, MD Orthopedic Oncologist
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Bone Tumors
Juxtacortical (Periosteal) Chondrosarcoma

James C. Wittig, MD
Sarcoma Surgeon
Orthopedic Oncologist


JUXTACORTICAL/PERIOSTEAL

Similar to juxtacortical chondroma
Periosteal lesion – cortical erosion
Chondroid matrix calcification
Similar to periosteal ogs (no hair on end periosteal reaction)
Larger soft tissue mass/size (>3-4cm)
Intramedullary canal spared 

JUXTACORTICAL CHONDROSARCOMA
Definition: A malignant, subperiosteal cartilaginous tumor that lacks osteoid production and erodes the underlying cortical bone  (periosteal chondrosarcoma)
<2% of chondrosarcomas

Age: 15-63 (80% are >20 years old vs periosteal osteosarcoma and periosteal chondroma)
No sex predilection
Clinical: Painless, mass or swelling; 1/3 of patients have pain (pain rarely exceeds swelling)
Most Common Locations:
     Femur
     Humerus
     Pelvis
     Rib or foot



RADIOGRAPHIC PRESENTATION

Radiology:
      Metaphyseal
      Cortical erosion with sclerotic underlying cortex (saucer shaped defect)
      Matrix calcification
      Triangular sclerotic spur at margin of tumor
      >5cm in diameter; average size: 11 cm (vs periosteal chondroma that is usually <5cm)
      No hair on end periosteal reaction  (vs. chondroblastic osteosarcoma)
      Intramedullary canal is spared


Plain X-ray: Periosteal Chondrosarcoma of Distal Femur

  

Cortical Thickening at Periphery of Lesion

 

Erosion of Outer Cortex



JUXTACORTICAL CHONDROSARCOMA


DIFFERENTIAL DIAGNOSIS

Periosteal Chondroma
Periosteal Osteosarcoma


GROSS PATHOLOGY

Grossly lobulated, gray-white, translucent
Calcification is common
Underlying cortex eroded with irregular sclerotic reaction


MICROSCOPIC PATHOLOGY

Lobulated
Well differentiated, low grade, hyaline cartilage
Focally myxoid stroma
No osteoid production
Almost always grade 1 or 2
Rarely grade 3


Juxtacortical Chondrosarcoma

PROGNOSIS


Low rate of Mets
      Metastisizes most commonly to the lungs
           Most are low to intermediate grade tumors
     80-90% long term survival

TREATMENT

Wide Limb Sparing Resection whenever feasible
      Amputation may be indicated for very large, unresectable or recurrent tumors 
Chemotherapy and radiation are generally not used in treatment of periosteal chondrosarcoma
     Chemotherapy may be considered for Grade 3 tumors
     Postoperative radiation may be considered for large tumors that can not be removed with a wide margin

 

 

 
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