无声窦综合征的研究进展

T. Sridhar, B. Karthika, M. Pavani, A. Iswarya, D. Shoban, A. Priya
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引用次数: 0

摘要

无声窦综合征(SSS)是一种罕见的疾病,可导致面部不对称、单侧无痛性眼球内陷、眶底塌陷和复视,这代表了窦内慢性负压的慢性上颌窦肺不张。SSS也称为内爆窦。一些人认为上颌窦的先天性发育也可能是SSS发展的原因。其特征性影像学特征为上颌窦出口阻塞、窦混浊和窦壁向内回缩引起的体积损失。Ostium梗阻似乎在SSS的发展中起着关键作用。治疗包括眶底重建手术和功能性内窥镜鼻窦手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A review on silent sinus syndrome
Silent sinus syndrome (SSS) is a rare condition that causes facial asymmetry, unilateral painless enophthalmos, orbital floor collapse, and diplopia, which represent the chronic maxillary sinus atelectasis with chronic negative pressure within the sinus. SSS is also known as imploding antrum. Some believe that congenital development of the maxillary sinus may also be responsible for the development of SSS. Its characteristic imaging features are maxillary sinus outlet obstruction, sinus opacification, and volume loss caused by inward retraction of the sinus wall. Ostium obstruction appears to play a critical role in the development of SSS. Treatment involves reconstructive procedure of orbital floor and functional endoscopic sinus surgery.
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