Author(s)

Adeeb Khawaji, Hanin Alsini

Department of Pediatrics, King Fahd Armed Forces Hospital, Jeddah, KSA.

Sickle cell disease is a hemoglobinopathy that results in paroxysmal vascular occlusion and tissue infarction that can manifest in a plurality of tissues. Vasoocclusive crises in sickle cell disease commonly involve bone marrow of the long bones and vertebrae. Involvement of bones with less marrow space, including the bones of the orbit, is reported rarely in the literature and can closely mimic orbital cellulitis, both clinically and radiologically. The present case is a 3 years old boy, a known case of sickle cell disease, who presented with what was thought to be orbital cellulitis and was treated accordingly. Subtle radiologic features of sickle cell orbitopathy were initially overlooked, resulting in an incorrect diagnosis and a treatment delay for the patient. Correctly treated most cases resolve with no adverse effects. This case highlights the importance of maintaining a high index of suspicion in patients with known sickle cell disease, even when the presentation is not classic.

Sickle Cell Disease, Orbital Cellulitis, Orbital Infarction, Sickle Cell Orbitopathy

Khawaji, A. and Alsini, H. (2020) Acute Orbitopathy Manifesting as Periorbital Cellulitis in Sickle Cell Disease. Case Reports in Clinical Medicine, 9, 137-143. doi: 10.4236/crcm.2020.96020.