Osteosarkom

Imaging of
skull vault tumors in adults. Osteosarcoma. Secondary, “pagetic.” T1WI post-contrast (a and b). Aggressive, destructive, giant, and transdiploic lesion with extensive intra- and extracranial soft-tissue component containing iso to hypointense areas of probable necrosis (arrows in a and b) and deeply hypointense foci of suspected bone matrix (dashed arrows in b). Note the underlying abnormal calvarial bone with diffuse expansion, cortical thickening and heterogeneous multifocal variable signal intensity, and enhancement (arrowheads) consistent with Paget disease
insightsimaging.springeropen.com • CC-by-4.0
Tumor and
tumorlike conditions of the pleura and juxtapleural region: review of imaging findings. Diagnosis: osteosarcoma. Technique: standard chest radiography and contrast-enhanced chest CT. Description: A 50-year-old man presented with complaints of right-sided chest pain. The postero-anterior chest radiograph (a) shows a large mass located at the lateral side of the right hemithorax with an associated pleural effusion. Note also a lytic expansion of the 8th left rib. The axial contrast-enhanced CT in the mediastinal window setting (b) confirms the heterogeneous mass with intralesional necrosis and calcifications originating from the 7th right rib, with focal expansive destruction, best seen in the bone window (c). There is a known pleural effusion with adjacent compression atelectasis of the right lower lobe. Histopathologic examination of the large mass confirmed the diagnosis of an osteosarcoma. The expansive tumorlike lytic lesion of the 8th left rib corresponds with fibrous dysplasia
insightsimaging.springeropen.com • CC-by-4.0
Teenager with
a limp after fallingAP and lateral radiographs of the right femur shows permeative cortical destruction throughout the diaphysis of the femur with associated diffuse sunburst periosteal reaction and a Codman’s triangle.The diagnosis was osteosarcoma of the femur.
pediatricimaging.org • CC-by-nc-sa 4.0
Teenager with
back painAP and lateral radiographs of the lumbar spine taken during a CT myelogram show loss of height of the L3 vertebral body and sclerosis of its posterior elements. Axial CT myelogram through the L3 vertebral body shows lytic lesions in the vertebral body and an expansile sclerotic appearance of the posterior elements with periosteal reaction.The diagnosis was osteosarcoma of the spine.
pediatricimaging.org • CC-by-nc-sa 4.0
Teenager who
after bumping their leg 1 year ago has had a painful lump in the shin. AP radiograph of the tibia and fibula (left) with a magnified view (right) shows a lesion in the diaphysis of the tibia with permeative cortical destruction and associated periosteal reaction and a Codman’s triangle.The diagnosis was osteosarcoma of the tibia.
pediatricimaging.org • CC-by-nc-sa 4.0
Radiopaedia • CC-by-nc-sa 3.0 • de

Osteosarcomas are malignant bone-forming tumors. They are the second most common primary bone tumor after multiple myeloma, accounting for ~20% of all primary bone tumors. They can be classified into primary and secondary forms, as well as histologic types, of which conventional osteosarcoma is the most common.

Epidemiology

Primary osteosarcoma typically occurs in young patients (10-20 years) with 75% taking place before the age of 20 because the growth centers of the bone are more active during puberty/adolescence .There is a slight male predominance.

Secondary osteosarcoma occurs in the elderly, usually secondary to malignant degeneration of Paget disease, extensive bone infarcts, post-radiotherapy for other conditions, osteochondroma, and osteoblastoma.

Associations

Clinical presentation

Patients often present with bone pain, occasionally accompanied by a soft-tissue mass or swelling. At times, the first symptoms are related to pathologic fracture.

Pathology

Location

Primary osteosarcomas typically occur at the metadiaphysis of long bones in the appendicular skeleton, most commonly at the following sites:

  • femur: ~40% (especially distal femur)
  • tibia: ~16% (especially proximal tibia)
  • humerus: ~15% 

Other sites are less common:

Secondary tumors, on the other hand, have a much wider distribution, largely mirroring the combined incidence of their underlying conditions, and thus much have a higher incidence in flat bones, especially the pelvis (a favorite site of Paget disease).

Osteosarcomas can be further categorized by anatomic relationship to the bone:

Classification

The WHO classification of bone tumors lists the histologic types of osteosarcoma, which can be further organized by the state of underlying bone and site of origin within the bone:

Conventional osteosarcomas can be further divided by histological subtype:

  • osteoblastic (most common)
  • chondroblastic
  • fibroblastic
Macroscopic appearance

Osteosarcomas are bulky tumors where a heterogeneous cut surface demonstrates areas of hemorrhage, fibrosis, and cystic degeneration. Their extension within the medullary cavity is often much more extensive than the bulky part of the tumor would suggest. Areas of bone formation are characteristic of osteosarcomas, with the degree of bone formation varying widely.

Microscopic appearance

Poorly formed trabecular bone is seen with (in the typical high-grade conventional subtype) cellular pleomorphism and mitoses. Variable amounts of fibrocystic and chondroblastic appearing cells may also be encountered.

Markers

Serum alkaline phosphatase (ALP) may be raised (particularly with advanced disease).

Radiographic features

Although plain radiography can provide a lot of information, MRI is used for local staging by assessing intraosseous tumor extension (e.g. growth plate/epiphysis, skip lesions) and soft-tissue involvement. Chest CT and bone scanning have a role in distant staging.

Plain radiograph

Conventional radiography continues to play an important role in diagnosis. Typical appearances of conventional high-grade osteosarcoma include:

CT

The role of CT is predominantly utilized in assisting biopsy and staging. CT adds little to plain radiography and MRI in the direct assessment of the tumor. The exception to this rule is predominantly lytic lesions in which small amounts of mineralized material may be inapparent on both plain film and MRI .

MRI

MRI is proving an essential tool to determine accurate local staging and assessment for limb-sparing resection, particularly for evaluation of intraosseous tumor extension and soft-tissue involvement. Evaluation of the growth plate is also essential as up to 75-88% of metaphyseal tumors do cross the growth plate into the epiphysis .

  • T1
    • soft tissue non-mineralized component: intermediate signal intensity
    • mineralized/ossified components: low signal intensity
    • peritumoral edema: intermediate signal intensity
    • scattered regions of hemorrhage will have a variable signal (see aging blood on MRI)
    • enhancement: solid components enhance
  • T2
    • soft tissue non-mineralized component: high signal intensity
    • mineralized/ossified components: low signal intensity
    • peritumoral edema: high signal intensity

Treatment and prognosis

Cure, if achievable, requires aggressive surgical resection often with amputation followed by chemotherapy. If a limb-salvage procedure is feasible, a course of multidrug chemotherapy precedes surgery to downstage the tumor, followed by wide resection of the bone and insertion of an endoprosthesis. The outcome depends on different factors such as age, sex, site, size, and type but the most important predictor is the histologic degree of necrosis post-induction chemotherapy; 90% histologic necrosis is associated with much better prognosis . Currently, the 5-year survival rate after adequate therapy is approximately 60-80% .

The most frequent complications of conventional osteosarcoma are a pathologic fracture and the development of metastatic disease, particularly to bone, lung, and regional lymph nodes.

Differential diagnosis

General differential considerations include the following:

When the lesion is at the posteromedial distal femur, consider

Practical points

When planning to biopsy a potential sarcoma, the treating surgeon should be consulted to plan the biopsy track as this will require excision to reduce the chance of seeding. A poorly planned track that crosses compartments can result in a more extensive resection, potentially with poor outcomes for the patient.

Siehe auch:
und weiter:
Assoziationen und Differentialdiagnosen zu Osteosarkom:
Ewing-Sarkom
 
www.eurorad.org • CC by-nc-sa-4.0
Aneurysmatische
Knochenzyste
www.eurorad.org • CC by-nc-sa-4.0
parossales
Osteosarkom
insightsimaging.springeropen.com • Open Access
Osteosarkom
des Femurs
pediatricimaging.org • CC-by-nc-sa 4.0
maligne
Entartung fibröse Dysplasie
insightsimaging.springeropen.com • Open Access
Osteosarkom
der Tibia
bmccancer.biomedcentral.com • CC-by-4.0