Fibrosarcoma
General: Malignant tumor of fibrous connective ti 949c29j ssue; most commonly seen in persons 30 to 70 years old; frequent metastases to lung; true fibrosarcoma has a tendency to occur in children (better prognosis); most fibrosarcomas now would be classified as malignant fibrous histiocytomas.
Ocular: Paralysis of extraocular muscles; proptosis; orbital edema; erosion of orbital bony walls; increased intraorbital pressure; metastases to choroid/orbit.
Clinical: Tumors of mesenchymal soft tissues of the extremities, especially in the knee region; progressive pain; edema; tumors of the sinuses; tumors of the lungs.
Henderson JW. Orbital tumors, 2nd ed. New York: Brian C. Decker, 1980:183-l88.
Jakobiec FA, Tannenbaum M. The ultrastructure of orbital fibrosarcoma. Am J Ophthalmol 1974; 77:899-9l7.
Roy FH. Fibrosarcoma. In: Fraunfelder FT, Roy FH, eds. Current Ocular Therapy, 5th ed. Philadelphia: WB Saunders, 2000:337.
Winer JM, et al. Juvenile fibrosarcoma of the orbit and eyelid: a study of 5 cases. Arch Ophthalmol 1983; 101:253.
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