Parosteal osteosarcoma is a subtype of osteosarcoma and arises from the outer layer of the periosteum.
It is the most common type of juxtacortical or surface osteosarcoma and accounts for ~5% of all osteosarcomas. It typically presents in early adulthood and middle age with a peak incidence in the third decade. It affects females slightly more than males 9.
Patients usually present with a painless, slowly enlarging mass 9.
They are usually located at the metaphysis (80-90%), most commonly at the posterior aspect of the distal femur (60%), followed by either end of the tibia, and then the proximal humerus.
They are composed of a dense osteoid component attached to the outer cortex over a narrow zone. Parosteal osteosarcoma originates from the outer fibrous layer of periosteum. It exhibits extensive bone matrix and minimal fibroblastic cellular atypia, and as such is considered to be a low-grade tumor.
- large lobulated exophytic, 'cauliflower-like' mass with central dense ossification adjacent to the bone
- string sign: thin radiolucent line separating the tumor from the cortex, seen in 30% of cases
- tumor stalk: grows within tumor in late stages and obliterates the radiolucent cleavage plane
- +/- soft tissue mass
- cortical thickening without aggressive periosteal reaction is often seen
- tumor extension into the medullary cavity is frequently seen
It exhibits predominantly low signal intensity both on T1 and T2 weighted imaging. High signal intensity on T2 is suggestive of a high-grade tumor.
Treatment and prognosis
Parosteal osteosarcomas are usually low-grade lesions are usually treated with surgical resection and no neoadjuvant chemotherapy or radiation. As they are frequently metaphyseal in location, large parosteal osteosarcomas or those with deep medullary invasion may require limb salvage, including joint replacement.
Parosteal osteosarcomas have an excellent prognosis (80-95% long-term survival).
On imaging consider
- cortical desmoid: avulsive injury of the posterior femoral cortex
- myositis ossificans: the ossification pattern of parosteal OS is the radiographic inverse of that seen in myositis ossificans, with the densest ossification in the center of the lesion and the least radio-opaque bone at the periphery (eggshell pattern); there is also often a history of trauma, progressive decrease in size or constant size and significant edema in early stages on MRI.
- sessile osteochondroma: parosteal OS lacks corticomedullary continuity between the tumor and the underlying medullary canal.
- juxtacortical chondrosarcoma
- high-grade surface osteosarcoma
- parosteal lipoma: radiolucent mass adjacent to the cortical surface on plain film and on cross-sectional imaging will usually show a definite fat component 2
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- 5. Lin J, Yao L, Mirra JM et-al. Osteochondromalike parosteal osteosarcoma: a report of six cases of a new entity. AJR Am J Roentgenol. 1998;170 (6): 1571-7. AJR Am J Roentgenol (abstract) - Pubmed citation
- 6. Dönmez FY, Tüzün U, Başaran C et-al. MRI findings in parosteal osteosarcoma: correlation with histopathology. Diagn Interv Radiol. 2008;14 (3): 142-52. Diagn Interv Radiol (link) - Pubmed citation
- 7. Jee WH, Choe BY, Ok IY et-al. Recurrent parosteal osteosarcoma of the talus in a 2-year-old child. Skeletal Radiol. 1998;27 (3): 157-60. - Pubmed citation
- 8. Yarmish G, Klein MJ, Landa J et-al. Imaging characteristics of primary osteosarcoma: nonconventional subtypes. Radiographics. 2010;30 (6): 1653-72. doi:10.1148/rg.306105524 - Pubmed citation
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Related Radiopaedia articles
The differential diagnosis for bone tumors is dependent on the age of the patient, with a very different set of differentials for the pediatric patient.
- bone-forming tumors
- cartilage-forming tumors
- chondromyxoid fibroma
- juxtacortical chondroma
- fibrous bone lesions
- bone marrow tumors
- other bone tumors or tumor-like lesions
- aneurysmal bone cyst
- benign fibrous histiocytoma
- giant cell tumor of bone
- Gorham massive osteolysis
- haemophilic pseudotumour
- intradiploic epidermoid cyst
- intraosseous lipoma
- musculoskeletal angiosarcoma
- musculoskeletal hemangiopericytoma
- primary intraosseous hemangioma
- post-traumatic cystic bone lesion
- simple bone cyst
- impending fracture risk