Frontal bone infarctions masquerading as bilateral orbital cellulitis in a patient with sickle cell disease

We report the appearance of orbital bone infarction intraoperatively in the case of an 18-year-old Saudi male patient who has been diagnosed with SCD and presented with severe headaches and generalized body aches. He was admitted with a case of SCD with acute VOC and started on the hospital sickle cell protocol. During the admission, the patient developed bilateral periorbital swelling and left inferior dystopia secondary to bilateral frontoparietal bone infarction, which was evident on the magnetic resonance imaging.
Source: Middle East African Journal of Ophthalmology - Category: Opthalmology Authors: Source Type: research