Asteris Petros, Bagli Eleni, Kalogeropoulos Chris
Department of Ophthalmology, University Hospital of Ioannina, Ioannina, GRC.
Cureus. 2025 Jun 3;17(6):e85282. doi: 10.7759/cureus.85282. eCollection 2025 Jun.
In this article, we present a rare case of posterior scleritis presenting as acute angle-closure glaucoma, highlighting the diagnostic challenges, clinical findings, and therapeutic approach, while emphasizing the importance of imaging modalities and detailed systemic evaluation. A 52-year-old, one-eyed, diabetic patient presented to the emergency department with mild ocular pain, photophobia, elevated intraocular pressure in the right eye, and a somewhat shallow anterior chamber. During examination, papilledema was noted. The patient was admitted for evaluation and management. During hospitalization, the patient's condition deteriorated rapidly, with significant worsening in visual acuity and uncontrolled intraocular pressure elevation. Detailed ophthalmologic and systemic evaluations were performed, which included optical coherence tomography (OCT), B-mode ultrasonography (u/s B-mode), ultrasound biomicroscopy (UBM), fundus fluorescein angiography (FFA), and magnetic resonance imaging (MRI) of the eyes and orbit. Initial findings included optic disc edema, a shallow anterior chamber, and serous retinal detachment extending from the macula to the periphery. U/S B-mode revealed the characteristic "T-sign" indicative of posterior scleritis. MRI of the orbit and UBM revealed inward dislocation of the ciliary body and the presence of fluid in the suprachoroidal space of the right eye. Laboratory tests ruled out infectious and systemic autoimmune causes. Treatment for posterior scleritis led to significant improvement in visual acuity and intraocular pressure (IOP), along with gradual resolution of symptoms. Over nine months of follow-up, the patient remained stable. Posterior scleritis is a rare but important differential diagnosis in cases of acute angle-closure glaucoma with arduous IOP control. In such cases, imaging modalities such as u/s B-mode and UBM are crucial for diagnosis and management. Early recognition and an appropriate therapeutic approach can lead to favorable outcomes even in atypical presentations.
在本文中,我们报告了一例罕见的后巩膜炎表现为急性闭角型青光眼的病例,强调了诊断挑战、临床发现及治疗方法,同时突出了影像学检查及详细全身评估的重要性。一名52岁的独眼糖尿病患者因右眼轻度眼痛、畏光、眼压升高及前房稍浅而就诊于急诊科。检查时发现视乳头水肿。患者入院进行评估和治疗。住院期间,患者病情迅速恶化,视力显著下降,眼压升高且难以控制。进行了详细的眼科及全身评估,包括光学相干断层扫描(OCT)、B型超声检查(B超)、超声生物显微镜检查(UBM)、眼底荧光血管造影(FFA)以及眼部和眼眶的磁共振成像(MRI)。初始检查结果包括视盘水肿、前房浅以及从黄斑延伸至周边的浆液性视网膜脱离。B超显示了提示后巩膜炎的特征性“T征”。眼眶MRI和UBM显示右眼睫状体向内移位以及脉络膜上腔有积液。实验室检查排除了感染性和全身性自身免疫性病因。后巩膜炎的治疗使视力和眼压得到显著改善,症状也逐渐缓解。经过九个月的随访,患者病情保持稳定。后巩膜炎在眼压难以控制的急性闭角型青光眼病例中是一种罕见但重要的鉴别诊断。在此类病例中,B超和UBM等影像学检查对于诊断和治疗至关重要。即使在非典型表现的情况下,早期识别和恰当的治疗方法也可带来良好的治疗效果。