A 62-year-old woman with periorbital and preseptal edema and erythema.

Q3 Medicine
Digital journal of ophthalmology : DJO Pub Date : 2025-07-07 eCollection Date: 2025-01-01 DOI:10.5693/djo.03.2024.06.006
Ross Mellman, Ali A Mohamed, Fahad Bhullar, Jonathan Berger
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引用次数: 0

Abstract

We report the case of a 62-year-old woman with a past medical history of leukemia, stem cell transplant, donor lymphocyte infusion, meningioma, and a prior episode of Sweet syndrome (SwS). She presented with progressive erythema, crusting, and edema in the preseptal and periorbital regions of her left eye. After initial treatment for presumed preseptal cellulitis with broad-spectrum antibiotics, the patient's symptoms worsened and became bilateral. The absence of systemic infectious signs and lack of clinical improvement raised suspicion for an alternative etiology. Given her history of SwS, a trial of systemic corticosteroids was initiated, resulting in a rapid clinical improvement. The diagnosis of cellulitis was subsequently rejected, and an ophthalmologic manifestation of SwS was suspected. This case highlights the importance of considering noninfectious inflammatory etiologies in patients with atypical or antibiotic-refractory periorbital symptoms-particularly in patients with a relevant medical history.

62岁女性,眼眶周围和鼻中隔水肿及红斑。
我们报告一位62岁女性,既往有白血病、干细胞移植、供体淋巴细胞输注、脑膜瘤和Sweet综合征(SwS)的病史。她表现为左眼鼻中隔和眶周区域进行性红斑、结痂和水肿。经初步治疗假定的间隔前蜂窝织炎与广谱抗生素,病人的症状恶化,并成为双侧。无全身性感染征象和缺乏临床改善引起了对其他病因的怀疑。考虑到她的SwS病史,开始了全身皮质类固醇的试验,导致临床迅速改善。蜂窝织炎的诊断随后被拒绝,并怀疑是SwS的眼科表现。本病例强调了在有非典型或抗生素难治性眼眶周围症状的患者中,特别是有相关病史的患者,考虑非感染性炎症病因的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Digital journal of ophthalmology : DJO
Digital journal of ophthalmology : DJO Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
14
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