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镰状细胞β-地中海贫血患儿眶骨梗死伪装为眶隔前蜂窝织炎。

Orbital bone infarction masquerading as preseptal cellulitis in a child with sickle beta-thalassaemia.

机构信息

Ophthalmology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia

Ophthalmology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.

出版信息

BMJ Case Rep. 2023 Mar 29;16(3):e252868. doi: 10.1136/bcr-2022-252868.

Abstract

Although several ophthalmic manifestations of sickle cell disease (SCD) are common, orbital bone infarction is rare. Orbital bones have less bone marrow creating an unlikely place to develop infarction. However, having a patient with SCD presenting with periorbital swelling should warrant imaging to rule out bone infarction. We present a case of a child with sickle beta-thalassaemia who was misdiagnosed with preseptal cellulitis in the right eye. Later upon review of the subtle signs of bone infarction in imaging, she was discovered to have orbital bone infarction.

摘要

虽然镰状细胞病(SCD)有几种眼部表现较为常见,但眶骨梗死却很少见。眶骨骨髓较少,因此不太可能发生梗死。但是,如果有 SCD 患者出现眶周肿胀,应进行影像学检查以排除骨梗死。我们报告了一例镰状细胞β-地中海贫血患儿,该患儿右眼被误诊为眶隔前蜂窝织炎。后来,在影像学检查中发现了细微的骨梗死迹象,才确诊为眶骨梗死。

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1
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