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

IF 2.3 Q1 OTORHINOLARYNGOLOGY Allergy & Rhinology Pub Date : 2020-01-14 eCollection Date: 2020-01-01 DOI:10.1177/2152656719899928
Nanki Hura, Omar G Ahmed, Nicholas R Rowan
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引用次数: 5

Abstract

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.

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无症状鼻窦综合征的不典型表现:1例报告及文献复习。
简介:沉默窦综合征(SSS)是一种以眼科学特征为特征的疾病,如自发性眼内陷和球下,伴同侧上颌窦不张,其他无症状表现。有文献表明,SSS继发于许多外部原因,包括创伤或手术,但在深咀嚼间隙潜在肿块的情况下,SSS的描述较少。病例介绍:56岁女性,慢性头痛病史,既往鼻窦影像学正常,表现为右侧面部疼痛加重,头痛辐射至枕部,主观视觉改变,尖锐耳痛,长期主观嗅觉减退。体格检查正常,鼻内窥镜检查显示右侧上颌内侧壁侧弯。磁共振成像显示,在咀嚼肌深部可见均匀的2 × 2 × 2.4 cm T1和t2加权的高强度肿块,显示右侧翼状肌内侧和外侧,可能为脂肪瘤病变。计算机断层扫描显示上颌窦不张和混浊,上颌后壁向内弯曲,一侧眼眶体积增大。在对上颌后间隙病变进行活检的同时,进行了内窥镜上颌窦造口术,几乎立即解决了患者的症状。肿块的组织学检查显示成熟的脂肪组织和少量良性小血管聚集。讨论:这是一种罕见的SSS,伴上颌后脂肪垫增大。在此,我们回顾了SSS的临床经验,并提供了SSS的表现、管理和围手术期注意事项的文献综述。
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
Allergy & Rhinology
Allergy & Rhinology OTORHINOLARYNGOLOGY-
CiteScore
3.30
自引率
4.50%
发文量
11
审稿时长
15 weeks
期刊最新文献
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