Strabbing E M, Engin O, Telleman M A J, Nagtegaal A P, Wolvius E B
Department of Oral and Maxillofacial Surgery, Special Dental Care and Orthodontics, University Medical Center Rotterdam, Dr. Molewaterplein 40, Rotterdam, 3015 GD, the Netherlands.
Department of Ophthalmology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Oral Maxillofac Surg. 2025 May 22;29(1):106. doi: 10.1007/s10006-025-01391-x.
Silent sinus syndrome (SSS) is a rare condition characterized by progressive maxillary sinus collapse, causing enophthalmos and hypoglobus without sinusitis symptoms. Secondary SSS arises from trauma or surgery disrupting mucociliary clearance. This study aims to analyze CT scan features, evaluate the timeline of SSS development, and identify contributing factors.
Patients diagnosed with secondary (post-traumatic or iatrogenic) SSS between January 2015 and January 2024 at the Erasmus Medical Center were reviewed. Characteristics from pre-SSS (T1) and post-SSS (T2) stages, management, and clinical outcomes were recorded. Data on patient demographics, symptoms, orthoptic findings, and the time interval between trauma or surgery and SSS onset were also collected.
Nine patients (six males and three females) met the inclusion criteria. The time from trauma or surgery to SSS onset ranged from one to thirty-six months, with a median of three months in the posttraumatic group. All patients presented with unilateral enophthalmos or hypoglobus; eight reported diplopia. Surgical management, including retrograde uncinectomy and orbital reconstruction, restored orbital anatomy and resolved symptoms.
Secondary SSS is a rare but significant condition requiring early recognition to prevent severe cosmetic and functional complications.
Secondary SSS should be considered when patients present with unexplained orbital changes following trauma or surgery. Regular follow-up is recommended, especially in patients with orbital trauma or surgery involving the inferomedial strut. Further studies are necessary to clarify risk factors associated with secondary SSS.
Not applicable.
寂静性鼻窦综合征(SSS)是一种罕见病症,其特征为上颌窦渐进性塌陷,导致眼球内陷和眼球低位,且无鼻窦炎症状。继发性SSS由创伤或手术破坏黏液纤毛清除功能引起。本研究旨在分析CT扫描特征,评估SSS发展的时间线,并确定相关因素。
回顾了2015年1月至2024年1月在伊拉斯谟医疗中心诊断为继发性(创伤后或医源性)SSS的患者。记录了SSS前(T1)和SSS后(T2)阶段的特征、治疗方法和临床结果。还收集了患者人口统计学数据、症状、斜视检查结果以及创伤或手术与SSS发病之间的时间间隔。
9例患者(6例男性和3例女性)符合纳入标准。从创伤或手术到SSS发病的时间为1至36个月,创伤后组的中位数为3个月。所有患者均出现单侧眼球内陷或眼球低位;8例报告有复视。手术治疗,包括逆行钩突切除术和眼眶重建,恢复了眼眶解剖结构并缓解了症状。
继发性SSS是一种罕见但严重的病症,需要早期识别以预防严重的美容和功能并发症。
当患者在创伤或手术后出现无法解释的眼眶变化时,应考虑继发性SSS。建议定期随访,尤其是眼眶创伤或涉及眶内侧支柱的手术患者。有必要进一步研究以阐明与继发性SSS相关的危险因素。
不适用。