Summary
Description
Fibrosarcoma is an uncommon, malignant spindle cell neoplasm which can present with different degrees of differentiation. Fibrosarcoma is found most commonly around the knee in the distal femur and proximal tibia followed by the pelvis.
People and Age
It presents in adults age 30 to 60 years old and affects men and women equally.
Symptoms and Presentation
It presents as a painful, localized mass.
Brief description of the xray
The radiologic picture of fibrosarcoma is that of an osteolytic lesion.
Tumor Name
Tumor Type
Benign or Malignant
Location in bone
Periosteal reaction
Complete Information on this Tumor
Introduction and Definition
Fibrosarcoma is an uncommon, malignant spindle cell neoplasm.The tumor produces a collagen matrix but does not produce osteoid or chondroid. Fibrosarcoma can be primary or secondary due to Paget's disease, fibrous dysplasia, irradiated giant cell tumor, bone infarct or chronic osteomyelitis. Fibrosarcoma occurs both as an intramedullary and periosteal lesion.
Incidence and Demographics
It appears in the metaphysis or metadiaphysis of long bones. Fibrosarcoma is found most commonly around the knee in the distal femur and proximal tibia followed by the pelvis. It presents in adults age 30 to 60 years old and affects men and women equally.
Symptoms and Presentation
The most common clinical presentation is that of a localized, painful mass.
X-Ray Appearance and Advanced Imaging Findings
The radiologic picture of fibrosarcoma is that of an osteolytic lesion. The margins can range from well-defined to ragged and moth-eaten. Periosteal reaction is seen with cortical destruction. Extension into the soft tissue is common. MRI helps define intraosseus spread and soft tissue extension. Bone scan demonstrates increased uptake. The differential diagnosis includes leiomyosarcoma, metastatic carcinoma, melanoma, malignant fibrous histiocytoma and multiple myeloma.
Histopathology findings
On gross examination the tumor is tan to grayish white with a rubbery consistency. Larger tumors may have hemorrhagic and necrotic foci.
As with plain x-ray, the microscopic appearance of fibrosarcoma varies with the level of differentiation. A well differentiated, low grade tumor has homogeneous spindle shaped fibroblasts with ovoid nuclei. There is little pleom orphism and infrequent mitoses in this slow growing form. The "herring bone pattern" of fascicles of cells is prominent. Poorly differentiated or high grade tumors have pleomorphic cells, abundant mitoses and hyperchromic nuclei. They metastasize early. The cellularity of the tumor is generally in inverse proportion to the collagen production. Tumors are graded from 1 to 4 on cellularity, nuclear atypia and mitoses with high grades carrying a worse prognosis.
As with plain x-ray, the microscopic appearance of fibrosarcoma varies with the level of differentiation. A well differentiated, low grade tumor has homogeneous spindle shaped fibroblasts with ovoid nuclei. There is little pleom orphism and infrequent mitoses in this slow growing form. The "herring bone pattern" of fascicles of cells is prominent. Poorly differentiated or high grade tumors have pleomorphic cells, abundant mitoses and hyperchromic nuclei. They metastasize early. The cellularity of the tumor is generally in inverse proportion to the collagen production. Tumors are graded from 1 to 4 on cellularity, nuclear atypia and mitoses with high grades carrying a worse prognosis.
Treatment Options for this Tumor
Treatment of fibrosarcoma includes radical surgical excision and adjuvant radiation therapy.
Outcomes of Treatment and Prognosis
Prognosis is largely dependent on the tumor grade
Suggested Reading and Reference
Kumar, R. et al., Fibrous Lesions of Bones, RadioGraphics, 10:237-256, March, 1990.
Marks, KE and TW Bauer, Fibrous Tumors of Bone, Orthopedic Clinics of North America, 20(3):377 393, July 1989.
Bulloughs, Peter, Orthopaedic Pathologv (third edition), Times Mirror International Publishers Limited, London, 1997.
Huvos, Andrew, Bone Tumors: Diagnosis. Treatment and Prognosis, W.B. Saunders, Co., 1991.
Marks, KE and TW Bauer, Fibrous Tumors of Bone, Orthopedic Clinics of North America, 20(3):377 393, July 1989.
Bulloughs, Peter, Orthopaedic Pathologv (third edition), Times Mirror International Publishers Limited, London, 1997.
Huvos, Andrew, Bone Tumors: Diagnosis. Treatment and Prognosis, W.B. Saunders, Co., 1991.
