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Atypical Presentation of Silent Sinus Syndrome: A Case Report and Literature Review

机译:无声窦综合征的非典型介绍:案例报告和文献综述

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Introduction Silent sinus syndrome (SSS) is a condition characterized by ophthalmologic features, such as spontaneous enophthalmos and hypoglobus with ipsilateral maxillary sinus atelectasis and an otherwise asymptomatic presentation. SSS has been documented secondary to a number of external causes, including trauma or surgery, but has less commonly been described in the setting of a potential mass in the deep masticator space. Case Presentation A 56-year-old woman with a history of chronic headaches with normal prior sinonasal imaging presented with increasing right-sided facial pain and headaches that radiated to her occiput, subjective visual changes, sharp ear pain, and long-standing subjective diminished sense of smell. Physical examination was normal, while nasal endoscopy demonstrated lateral bowing of the medial maxillary wall on the right. Magnetic resonance imaging demonstrated a homogenous 2?×?2?×?2.4 cm T1- and T2-weighted, hyperintense mass lesion in the deep masticator space splaying the right medial and lateral pterygoid muscles concerning for a possible lipomatous lesion. Computed tomography revealed an atelectatic and opacified maxillary sinus with inward bowing of the posterior maxillary wall and increased orbital volume on that side. Endoscopic maxillary antrostomy was performed with biopsy of the retromaxillary space lesion and with near immediate resolution of the patient’s symptoms. Histologic examination of the mass demonstrated mature adipose tissue with few aggregates of benign small vessels. Discussion This is an unusual presentation of SSS, with an accompanying enlargement of the retromaxillary fat pad. We herein review our clinical experience with SSS and provide a literature review of the presentation, management, and perioperative considerations for SSS.
机译:引言无声窦综合征(SSS)是一种病症,其特征在于眼科特征,例如自发的嗜鼻肌和嗜血杆菌,具有同侧上颌窦大学和其他无症状的呈现。已经记录了SSS的次要到许多外部原因,包括创伤或手术,但在深层咀嚼物空间中的潜在质量的设置中已经不太描述。案例介绍一个56岁的女性,具有正常的先前Sinonasal成像的慢性头痛的历史,随着右侧的面部疼痛和辐射到她的枕骨,主观视觉变化,尖锐的耳痛和长期主观减少嗅觉。体检是正常的,而鼻内镜检查表明右侧上颌壁的横向弯曲。磁共振成像显示出均匀的2?×2?2?×β2?×2.4cm t1和t2加权,深染色体空间中的高压质量病变,展开了用于可能的脂质病变的右侧和侧翼肌肉。计算机断层摄影揭示了一部分和薄片的上颌窦,上颌壁向内弯曲,并在该侧增加了轨道体积。用抗摩阳度损伤的活组织检查进行内窥镜上颌骨束术,并近在咫尺的患者症状。对质量的组织学检查显示成熟的脂肪组织与良性小血管的少量聚集体。讨论这是SSS的不寻常呈现,伴随抗摩缩脂肪垫的扩大。我们在此方面审查了我们对SSS的临床经验,并为SSS的演示,管理和围手术期考虑进行了文献综述。

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