Systemic diseases, primary orbital diseases and extraorbital lesions extending into the orbit may lead to ocular proptosis. Eleven patients with ocular proptosis caused by non previously treated extraorbital malignant tumors were studied with computed tomography. Nonepithelial neoplasms were the most common tumors (82%) including three rabdomyosarcomas (27%), three non-Hodgkin's lymphomas (27%), and other sarcomas in two patients (18%). Squamous cell carcinoma (9%), Burkitt's lymphoma (9%) and poorly differentiated carcinoma (9%) were also identified. The most common primary sites of the tumors were the sinonasal cavities (nine cases; 82%), particularly the ethmoidal sinus (five cases). Ocular proptosis was the only ophthalmic sign in four patients (36%) whereas one patient had bilateral ocular proptosis as the only sign of disease. Seventeen orbits were involved due to six patients had bilateral tumor extension into the orbits. Tumor extension into the orbits was mainly through the orbital bone (16 orbits; 94%). There was involvement of all compartments in most of the orbits (59%). The tumor was extraconal in 16 orbits. Computed tomography revealed ocular proptosis in 15 of the 17 orbits (88%), which was bilateral in four cases (eight orbits). Grade 2 ocular proptosis was observed in seven patients (47%). Forty-four regions of the face and skull were involved, excluding the orbits and the primary site of the tumor, indicating extensive loco-regional disease at the time of the diagnosis.
Ocular proptosis; Malignant tumors; Orbital extension
