Telangiectatic osteosarcoma

Telangiectatic osteosarcomas (TOS) are an uncommon variant of osteosarcoma that represent 2.5-12% of all osteosarcomas. 

Telangiectatic osteosarcomas have similar demographics to that of conventional osteosarcoma and typically presents in adolescents and young adults (reported age range of 3-67 years with a mean age of 20 years). There is a recognized male predilection.

Most osteosarcomas have a small telangiectatic component but in order to classify as telangiectatic osteosarcoma, the telangiectatic component should comprise >90% 1.

Most of the tumor comprises of large blood-filled spaces separated by thin bony septations.

Microscopically the tumor consists of vascular sinusoids surrounded by thin septa, osteoid matrix and cells with significant pleomorphism and high mitotic rate.

Telangiectatic osteosarcoma can be a secondary lesion (arising in association with fibrous dysplasiaPaget disease, or post-radiation therapy).

Most common locations by site are: 

  • around knee:
    • femur: 50-62%
    • tibia: 10-25%
  • humerus: 12-16%

In terms of location within bone:

  • metaphyseal: ~80%
  • diaphyseal: ~20% 

Typically seen as an expansile lytic bone lesion at the metaphysis:

  • geographic bony destruction with wide zone of transition tends to be more common than permeative bony destruction 6
  • less osteoid matrix than conventional type
  • pathological fractures are frequent
  • low attenuating fluid-fluid levels within the lesion (in ~80% of cases)
  • useful at assessing associated cortical destruction
  • thick peripheral and nodular septal enhancement
  • osteoid matrix mineralization
  • commonly shows fluid-fluid levels within the lesion (~90% of cases) with variable signal intensity
  • allows appreciation of surrounding soft tissue components
  • signal characteristics are often heterogeneous
  • enhancement of septa as well as the soft tissue component may be observed
  • hemorrhage appears as hyperintense on T1 and variable signal intensity on T2

Overall, lesions tend to show marked but heterogeneous uptake on bone scans. May demonstrate a region of central photopenia representing a doughnut sign 3,6.

The treatment of telangiectatic osteosarcoma is often similar to that of conventional osteosarcoma: chemotherapy followed by wide surgical resection and limb salvage or amputation. 

Survival rate of telangiectatic osteosarcoma (estimated at ~70%) is similar to that of conventional osteosarcoma.

They are associated with a high rate of pathological fractures 4.

First described by Sir James Paget (1814-1899), an English surgeon, in 1854 7.

Considerations on plain film include:

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Article information

rID: 10830
Synonyms or Alternate Spellings:
  • Telangiectatic type osteosarcoma
  • Teleangiectatic osteosarcoma (TOS)

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