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Year : 2020  |  Volume : 68  |  Issue : 11  |  Page : 2536

Enophthalmos in silent brain syndrome

Department of Ophthalmology, Federal University of Goias, Brazil

Date of Web Publication26-Oct-2020

Correspondence Address:
Leonardo Lando
Federal University of Goias, Primeira Avenida s/n, Goiania - 74605-020
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijo.IJO_897_20

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How to cite this article:
Lando L, Paiva MO, Pereira LS. Enophthalmos in silent brain syndrome. Indian J Ophthalmol 2020;68:2536

How to cite this URL:
Lando L, Paiva MO, Pereira LS. Enophthalmos in silent brain syndrome. Indian J Ophthalmol [serial online] 2020 [cited 2020 Nov 30];68:2536. Available from: https://www.ijo.in/text.asp?2020/68/11/2536/299118

No related papers from this study have been published before this submission for Indian Journal of Ophthalmology.

A 56-year-old man underwent a shunting procedure in childhood due to hydrocephalus secondary to meningitis. Along the following years, he manifested recurrent tearing, foreign body sensation, and slow “eye shrinking”. External clinical exam confirmed enophthalmos, poor lid apposition to the globe, and inferior ectropion bilaterally [Figure 1]a. Biomicroscopy showed dry eye syndrome bilaterally. Computed tomography scans of the brain and orbits revealed ventriculomegaly (asterisks), ventriculoperitoneal shunt valves (one implant at arrow), posterior displacement of eyeballs, and significant orbital remodeling [Figure 1]b. The patient was diagnosed with silent brain syndrome, a rare form of progressive enophthalmos after intracranial pressure resolution.[1],[2]
Figure 1: (a) Lateral view photo exhibits prominent enophthalmos due to the syndrome (b) CT scan displays brain changes related to the significant orbital volume reductionsw

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Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

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Conflicts of interest

There are no conflicts of interest.

  References Top

Pargament JM, Peralta RJ, Nerad JA, McCann JD. Orbital volume augmentation for enophthalmos following ventriculoperitoneal shunting: A case study in “silent brain syndrome”. Ophthalmic Plast Reconstr Surg 2017;33(3S Suppl 1):S168-71.  Back to cited text no. 1
Bernardini FP, Rose GE, Cruz AA, Priolo E. Gross enophthalmos after cerebrospinal fluid shunting for childhood hydrocephalus: The “silent brain syndrome”. Ophthalmic Plast Reconstr Surg 2009;25:434-6.  Back to cited text no. 2


  [Figure 1]


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