Case reports in ophthalmology · 2026
Sickle Cell Crisis-Induced Painless Bilateral Orbital Bone Infarction: A Case Report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Farson Luke, Shenouda Marina, Kakouri Agni, Kashanchi Ashkan, Sitton Clark, McCulley Timothy, Chen Ying
Аннотация
INTRODUCTION: Sickle cell disease is associated with painful vaso-occlusive crises, bone infarction, avascular necrosis, and osteomyelitis. Sickle cell orbitopathy is a rare manifestation with signs similar to periorbital cellulitis and has subtle radiologic features.
CASE PRESENTATION: We report a case of a five-year-old girl with sickle cell who presented with bilateral orbital infarctions and subperiosteal hematomas, notably without periorbital pain, and was treated with antibiotics and steroids.
CONCLUSION: Physicians should be aware of this rare manifestation, especially in the pediatric population, as it can affect subsequent management.
CASE PRESENTATION: We report a case of a five-year-old girl with sickle cell who presented with bilateral orbital infarctions and subperiosteal hematomas, notably without periorbital pain, and was treated with antibiotics and steroids.
CONCLUSION: Physicians should be aware of this rare manifestation, especially in the pediatric population, as it can affect subsequent management.