02 November 2023
: Case report 
Painless Orbital Bone Infarction in a Child with Sickle Cell Anemia: A Case of Misdiagnosed Periorbital Cellulitis
Challenging differential diagnosis, Unusual setting of medical care, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
Khalid Alsaggaf1ADEFG*, Hazem Aljuhani2ABDEFG, Abeer Aljahdali3ABDEFG, Manal Hadrawi4ABDEFG, Wasayf Almehmadi2ADEFGDOI: 10.12659/AJCR.939595
Am J Case Rep 2023; 24:e939595
Figure 4. Magnetic resonance imaging with contrast. Bilateral subperiosteal heterogeneous collections were visible on an MRI with contrast: a large collection in the superolateral wall of the left orbit (2×0.8×2.1 cm) and a small collection in the inferolateral wall of the right orbit (1×0.6 cm). Both collections had intermediate-to-high T1 signal intensities and high T2 signal intensities. Additionally, the sphenoid and lateral orbital walls have both had bilateral osseous changes.