The imploding antrum: An unusual case of nontraumatic painless enophthalmos

The imploding antrum or silent sinus syndrome is a rare phenomenon that presents with spontaneous painless enophthalmos and hypoglobus. It occurs due to ipsilateral maxillary antral atelectasis secondary to asymptomatic obstructive chronic sinus mucosal disease. Ophthalmologists, otorhinolaryngologi...

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Main Authors: Debraj Sen, Vijinder Arora, Saurabh Adlakha, Harleen Miglani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Indian Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=10;spage=786;epage=788;aulast=Sen
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spelling doaj-ace55f386cbb4a25b2eea68bb21ea7162020-11-25T00:15:35ZengWolters Kluwer Medknow PublicationsIndian Journal of Ophthalmology0301-47381998-36892016-01-01641078678810.4103/0301-4738.195015The imploding antrum: An unusual case of nontraumatic painless enophthalmosDebraj SenVijinder AroraSaurabh AdlakhaHarleen MiglaniThe imploding antrum or silent sinus syndrome is a rare phenomenon that presents with spontaneous painless enophthalmos and hypoglobus. It occurs due to ipsilateral maxillary antral atelectasis secondary to asymptomatic obstructive chronic sinus mucosal disease. Ophthalmologists, otorhinolaryngologists, and radiologists must be aware of this entity. This article illustrates the typical presentation in a 17-year-old male with unilateral ptosis and a deep superior sulcus, and characteristic imaging findings of ipsilateral increased orbital volume and depression of the orbital floor, maxillary sinus opacification and atelectasis with retraction of the posterolateral and medial walls, lateralization of the uncinate process, and obstruction of the ostiomeatal unit. This is probably the first time that the syndrome is being reported in such a young person. The pathogenesis, differential diagnosis, and treatment modalities of this entity are also reviewed.http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=10;spage=786;epage=788;aulast=SenAtelectasisenophthalmoshypoglobusmaxillary antrum
collection DOAJ
language English
format Article
sources DOAJ
author Debraj Sen
Vijinder Arora
Saurabh Adlakha
Harleen Miglani
spellingShingle Debraj Sen
Vijinder Arora
Saurabh Adlakha
Harleen Miglani
The imploding antrum: An unusual case of nontraumatic painless enophthalmos
Indian Journal of Ophthalmology
Atelectasis
enophthalmos
hypoglobus
maxillary antrum
author_facet Debraj Sen
Vijinder Arora
Saurabh Adlakha
Harleen Miglani
author_sort Debraj Sen
title The imploding antrum: An unusual case of nontraumatic painless enophthalmos
title_short The imploding antrum: An unusual case of nontraumatic painless enophthalmos
title_full The imploding antrum: An unusual case of nontraumatic painless enophthalmos
title_fullStr The imploding antrum: An unusual case of nontraumatic painless enophthalmos
title_full_unstemmed The imploding antrum: An unusual case of nontraumatic painless enophthalmos
title_sort imploding antrum: an unusual case of nontraumatic painless enophthalmos
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Ophthalmology
issn 0301-4738
1998-3689
publishDate 2016-01-01
description The imploding antrum or silent sinus syndrome is a rare phenomenon that presents with spontaneous painless enophthalmos and hypoglobus. It occurs due to ipsilateral maxillary antral atelectasis secondary to asymptomatic obstructive chronic sinus mucosal disease. Ophthalmologists, otorhinolaryngologists, and radiologists must be aware of this entity. This article illustrates the typical presentation in a 17-year-old male with unilateral ptosis and a deep superior sulcus, and characteristic imaging findings of ipsilateral increased orbital volume and depression of the orbital floor, maxillary sinus opacification and atelectasis with retraction of the posterolateral and medial walls, lateralization of the uncinate process, and obstruction of the ostiomeatal unit. This is probably the first time that the syndrome is being reported in such a young person. The pathogenesis, differential diagnosis, and treatment modalities of this entity are also reviewed.
topic Atelectasis
enophthalmos
hypoglobus
maxillary antrum
url http://www.ijo.in/article.asp?issn=0301-4738;year=2016;volume=64;issue=10;spage=786;epage=788;aulast=Sen
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