Faculty, Staff and Student Publications

Language

English

Publication Date

1-1-2026

Journal

Case Reports in Ophthalmology

DOI

10.1159/000550138

PMID

41695127

PMCID

PMC12904658

PubMedCentral® Full Text Version

Post-print

Abstract

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.

Keywords

Sickle cell crisis, Orbital bone infarction, Infarctions, Case report

Published Open-Access

yes

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