Author/Authors :
Rajabi, Mohammad Taher Eye Research Center - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Poursayed Lazarjani, Zahra Eye Research Center - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Mohammadi, Saeed Eye Research Center - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Veshagh, Mohammad Eye Research Center - Labbafinejad Eye Hospital - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Hosseinzadeh, Farideh ENT and Head and Neck Research Center - The Five Senses Institute - Iran University of Medical Sciences, Tehran, Iran , Rafizadeh, Mohsen Eye Research Center - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Asadi Amoli, Fahimeh Department of Pathology - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Hosseini, Simindokht Eye Research Center - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Purpose: To present a patient with giant cell tumor (GCT) of the orbit by changing behavior from an intraorbital mass to an intraosseous tumor.
Methods: A 16‑year‑old boy presented with pain, swelling, erythematous of the left upper and lower eyelids, proptosis, and diplopia. Ophthalmic
examination revealed chemosis, conjunctival injection, limited elevation, depression as well as abduction in the left eye.
Results: Multislice computed tomography scan (CT scan) of the orbit and paranasal sinuses showed a hyperdense, oval, extraconal mass
with bone erosion. Magnetic resonance imaging of the orbit showed an inferior lateral isointense, oval, extraconal mass that had indented the
globe. The patient underwent superior lateral orbitotomy, and the orbital mass was excised. Two months later, the patient developed proptosis,
severe chemosis, and eyelid erythema in the same eye. CT scan showed an intraosseous mass in the lateral wall of the orbit that had pushed the
globe anteromedially. Intraosseous tumor was resected, and the lateral orbital wall was drilled during the second surgery. GCT was diagnosed
based on pathological survey.
Conclusion: Following the resection of the orbital GCT, the tumor behavior may change to an intraosseous lesion.
Keywords :
Diamond burr , Giant cell tumor , Intraosseous , Orbit