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一名患有寂静性窦综合征患者在人工耳蜗植入术后出现的眼眶并发症。

Orbital Complications After Cochlear Implant Surgery in a Patient With Silent Sinus Syndrome.

作者信息

Khurayzi Tawfiq, Algadhi Walaa H, Ghafiry Hassan, Ardi Khalid T, Aljazeeri Isra

机构信息

Otolaryngology - Head and Neck Surgery, Cochlear Implant Center, King Fahad Central Hospital, Jazan, SAU.

Otorhinolaryngology - Head and Neck Surgery, King Abdullah Ear Specialist Centre (KAESC) King Abdulaziz University Hospital, King Saud University, Riyadh, SAU.

出版信息

Cureus. 2024 Jul 17;16(7):e64724. doi: 10.7759/cureus.64724. eCollection 2024 Jul.

Abstract

Cochlear implantation is an effective procedure for treating patients with severe to profound sensorineural hearing loss. Silent sinus syndrome (SSS) is an uncommon disease that affects the maxillary sinus. It is diagnosed clinically and confirmed radiologically. This study describes the case of a four-year-old child who presented with bilateral profound congenital hearing loss with a family history of congenital hearing loss. The patient had no significant complaints regarding the paranasal sinuses or orbits. Radiological evaluation, including temporal bone computed tomography (CT) and magnetic resonance imaging (MRI) of the ear and internal auditory meatus, showed normal anatomy of the inner ear and petrous bone bilaterally. However, findings of SSS were incidentally detected in the left maxillary sinus. The patient underwent bilateral simultaneous cochlear implantation. On the second postoperative day, he developed left-sided ophthalmoplegia, pain on eye movement, mild proptosis, and upper and lower eyelid swelling with erythema and tenderness. The patient improved rapidly following antibiotic treatment and was almost normal by the fifth postoperative day with no notable findings; hence, he was discharged. Surgeons should carefully evaluate preoperative radiological images of the paranasal sinuses for any malformation or pathology, so that appropriate medical or surgical treatment can be given.

摘要

人工耳蜗植入是治疗重度至极重度感音神经性听力损失患者的有效方法。寂静性窦综合征(SSS)是一种影响上颌窦的罕见疾病。其通过临床诊断并经影像学检查确诊。本研究描述了一名4岁儿童的病例,该患儿患有双侧重度先天性听力损失且有先天性听力损失家族史。患者对鼻窦或眼眶无明显不适主诉。包括颞骨计算机断层扫描(CT)以及耳部和内耳道的磁共振成像(MRI)在内的影像学评估显示,双侧内耳和岩骨解剖结构正常。然而,左侧上颌窦偶然发现了寂静性窦综合征的表现。该患者接受了双侧同期人工耳蜗植入。术后第二天,他出现左侧眼肌麻痹、眼球运动时疼痛、轻度眼球突出以及上下眼睑肿胀伴红斑和压痛。经抗生素治疗后患者恢复迅速,术后第五天几乎恢复正常且无明显异常表现,因此出院。外科医生应仔细评估鼻窦的术前影像学图像,以发现任何畸形或病变,从而给予适当的药物或手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/994d/11328450/05225472af8e/cureus-0016-00000064724-i01.jpg

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