Bilateral acquired Brown's syndrome

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Identifier Bilateral_acquired_Brown's_syndrome_Walsh
Title Bilateral acquired Brown's syndrome
Subject Brown's syndrome; Brown syndrome; hypertropia; diplopia; disorder of ocular motility; Sjogren's syndrome
Creator Ryan D. Walsh, MDDepartment of Ophthalmology and Visual Sciences, The Eye Institute, Medical College of Wisconsin; Department of Neurology, Medical College of Wisconsin; Collin McClelland, MDDepartments of Ophthalmology and Visual Neurosciences. University of Minnesota, Minneapolis, Minnesota.
Description A 27 year old female with a history of Sjogren's syndrome reported a 2 year history of a vertical binocular diplopia with looking up-and-to-the right. She has also noticed an audible "click" when positioning her eyes in this direction. As depicted in the video, when attempting to look up-and-to-the-right, the left eye has moderate deficiency of supraduction; likewise, when attempting to look up-and-to-the-left, the right eye has mild deficiency of supraduction. On ocular alignment testing (Maddox Rod), there was no ocular misalignment in primary gaze, right gaze, or left gaze; however, in up-and-to-the-right gaze there was a right hyperdeviation of 25 prism diopters, and in up-and-to-the-left gaze there was a left hyperdeviation of 3 prism diopters. The patient was symptomatic with diplopia in up-and-to-the right-gaze, but not any other direction of gaze (including no diplopia in primary gaze). An MRI of the brain was negative. This patient has bilateral Brown's syndrome, which in her case was believed to be acquired, likely on an autoimmune basis related to inflammation of the bilateral trochlear region and associated with her Sjogren's syndrome. Brown's syndrome can be congenital or acquired, but is usually congenital. It is typically unilateral, though bilateral Brown's syndrome is occasionally encountered. Brown's syndrome is characterized by limitation of the ability to elevate the eye when it is in an adducted position, with normal (or near normal) elevation from a primary or abducted position. It is caused by mechanical "tethering" of the superior oblique muscle tendon sheath, which is unable to lengthen, causing limitation of elevation of the adducted eye (simulating an inferior oblique palsy). Ocular alignment in primary gaze is typically normal, though ipsilateral hypotropia can sometimes be seen (particularly in severe cases of Brown's syndrome). Patients may experience an audible click or pop, or experience discomfort or strain in the eye on attempted upgaze. The acquired form typically occurs when the superior oblique tendon/trochlea complex is affected by inflammation (such as in rheumatoid arthritis, or systemic lupus erythematosus), infection (ex. orbital infection or paranasal sinusitis), trauma, or surgery involving the superior eyelid or superonasal orbit. The presented case demonstrates an infrequent but recognized cause of Brown's syndrome.
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2016
Type Image/MovingImage
Format video/mp4
Rights Management Copyright 2016. For further information regarding the rights to this collection, please visit:
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL
ARK ark:/87278/s6jd85d3
Setname ehsl_novel_novel
Date Created 2016-06-02
Date Modified 2021-05-06
ID 187690
Reference URL
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