Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Extraskelectal osteosarcoma (pleural origin)
- Radiologic Findings
- Chest radiographies demonstrate rapidly growing pleural based mass with amorphous calcifications in the left lower hemithorax.
Initial chest CT images(mediastinal window setting) show bizarre shaped pleural calcifications, which are located the left diaphragmatic and lower lateral pleural space.
On follow-up CT after 7 months, the images(mediastinal window setting) demonstrate newly developed heterogenous enhancing masses arising from pleural calcifications in the left lower hemithorax. Contrast to previous CT images, pleural calcifications also slightly growing and extended.
- Brief Review
- The tumor was irregular shaped firm mass, measuring 8 x 6 x 4.5cm in size, which was broadly attached to left lower lobe and invaded diaphragm. The tumor extended to left 6th intercostal space and it was free from adjacent ribs. The tumor was easy to break, and included friable calcifications on the inside.
Photomicrograph of resected mass with H and E stain shows malignant spindle cell sarcoma with osteoid deposition and bone formation by pleomorphic tumor cells.
Extraskeletal osteosarcoma is a malignant mesenchymal soft-tissue neoplasm without attachment to the skeleton, which is able to produce osteoid or cartilaginous matrix. Hitologically, it is indistinguishable from osteogenic osteosarcoma, but, should be considered clinically and therapeutically separate from osteogenic osteosarcoma.
Extraskeletal osteosarcoma is a rare malignant neoplasm that accounts for approximately 1% of all soft-tissue sarcomas and 4% of osteogenic osteosarcomas. Unlike typical skeletal osteosarcomas, extraskeletal osteosarcoma affects older patients and usually presents in the sixth or the seventh decades.
Extraskeletal osteosarcoma may be asymptomatic or present with an enlarging mass or pain. The primary treatment of extraskeletal osteosarcoma is surgical resection. In addition, some patients are treated with chemotherapy or radiation therapy. Patients with extraskeletal osteosarcoma have a poor prognosis (5yrs survival rate < 40%), and more than half of the patients develop recurrences and metastases.
On radiographs, extraskeletal osteosarcoma often appears as soft-tissue opacity with variable amounts of mineralization (focal or extensive).
On CT, the tumor is separate from adjacent osseous structures and appears to have a pseudocapsule. Matrix mineralization is best appreciated on CT. On contrast-enhanced images, the tumor shows heteregeneous enhancement depending on the degree of necrosis.
On MRI, the tumor is usually a relatively well-circumscribed heterogeneous mass, which is isointense relative to skeletal muscle on T1-weighted images and isointense to mildly hyperintense on T2-weighted images. Hemorrage is not rare and may be represented by hyperintense foci on T1- and T2-weighted images.
- References
- 1. Grainne Mc Auley, Jyothi Jagannathan, Kevin O뭃egan, Katherine M. Krajewski, Nikhil Ramaiya. Extraskeletal Osteosarcoma: Spectrum of Imaging Findings. AJR January 2012 198:W31-W37
2. Bradley Sabloff, Reginald F. Munden, Amal I. Melhem. Radiologic뻇athologic Conferences of The University of Texas M. D. Anderson Cancer Center: Extraskeletal Osteosarcoma of the Pleura. AJR April 2003 180:972
3. Gregory W. Gladish, Bradley M. Sabloff, Reginald F. Munden, Mylene T. Truong. Primary Thoracic Sarcomas. Radiographics May 2002 22:3 621-637
- Keywords
- pleura, malignant tumor,