Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion

Purpose. Case report describing an eight-month-old infant presenting with intermittent esotropia and irritability who was found to have malignant (grade 4) hypertensive retinopathy and mid-aortic syndrome. Methods. Visual acuity was 6/140 in the right eye and not recordable in the left eye. Blood pr...

Full description

Saved in:
Bibliographic Details
Main Authors: Lawrence J. Oh, Gaurav Bhardwaj, David S. Winlaw, Craig E. Donaldson
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Ophthalmological Medicine
Online Access:http://dx.doi.org/10.1155/2016/8162687
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832549075321356288
author Lawrence J. Oh
Gaurav Bhardwaj
David S. Winlaw
Craig E. Donaldson
author_facet Lawrence J. Oh
Gaurav Bhardwaj
David S. Winlaw
Craig E. Donaldson
author_sort Lawrence J. Oh
collection DOAJ
description Purpose. Case report describing an eight-month-old infant presenting with intermittent esotropia and irritability who was found to have malignant (grade 4) hypertensive retinopathy and mid-aortic syndrome. Methods. Visual acuity was 6/140 in the right eye and not recordable in the left eye. Blood pressure was as high as 230/120 mmHg. Fundoscopy revealed bilateral optic disc swelling, macular stars, and serous retinal detachment in the left eye, findings that are consistent with malignant (grade 4) hypertensive retinopathy. CT abdominal angiogram revealed a severe mid-aortic syndrome with occlusion of the abdominal aorta at T12. Results. The patient was treated with medical management of his hypertension, improving the subretinal exudate. Binocular visual acuity improved to 6/9.5 over 9 months. There was a persistent left relative afferent pupillary defect and moderate left esotropia. Conclusion. This is the first reported case of malignant hypertensive retinopathy in an infant with concomitant mid-aortic occlusion. The authors emphasize the need for an ophthalmological and pediatric examination in a child presenting with intermittent squint and irritability. The esotropia was found to be a false localizing sign of raised intracranial pressure secondary to the severe mid-aortic syndrome.
format Article
id doaj-art-1621df7634e44b17ad14e4df3b368ba6
institution Kabale University
issn 2090-6722
2090-6730
language English
publishDate 2016-01-01
publisher Wiley
record_format Article
series Case Reports in Ophthalmological Medicine
spelling doaj-art-1621df7634e44b17ad14e4df3b368ba62025-02-03T06:12:16ZengWileyCase Reports in Ophthalmological Medicine2090-67222090-67302016-01-01201610.1155/2016/81626878162687Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic OcclusionLawrence J. Oh0Gaurav Bhardwaj1David S. Winlaw2Craig E. Donaldson3Department of Ophthalmology, Save Sight Institute, Sydney, NSW, AustraliaDepartment of Ophthalmology, The Children’s Hospital at Westmead, Sydney, NSW, AustraliaSydney Medical School, University of Sydney, Sydney, NSW, AustraliaSydney Medical School, University of Sydney, Sydney, NSW, AustraliaPurpose. Case report describing an eight-month-old infant presenting with intermittent esotropia and irritability who was found to have malignant (grade 4) hypertensive retinopathy and mid-aortic syndrome. Methods. Visual acuity was 6/140 in the right eye and not recordable in the left eye. Blood pressure was as high as 230/120 mmHg. Fundoscopy revealed bilateral optic disc swelling, macular stars, and serous retinal detachment in the left eye, findings that are consistent with malignant (grade 4) hypertensive retinopathy. CT abdominal angiogram revealed a severe mid-aortic syndrome with occlusion of the abdominal aorta at T12. Results. The patient was treated with medical management of his hypertension, improving the subretinal exudate. Binocular visual acuity improved to 6/9.5 over 9 months. There was a persistent left relative afferent pupillary defect and moderate left esotropia. Conclusion. This is the first reported case of malignant hypertensive retinopathy in an infant with concomitant mid-aortic occlusion. The authors emphasize the need for an ophthalmological and pediatric examination in a child presenting with intermittent squint and irritability. The esotropia was found to be a false localizing sign of raised intracranial pressure secondary to the severe mid-aortic syndrome.http://dx.doi.org/10.1155/2016/8162687
spellingShingle Lawrence J. Oh
Gaurav Bhardwaj
David S. Winlaw
Craig E. Donaldson
Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
Case Reports in Ophthalmological Medicine
title Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
title_full Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
title_fullStr Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
title_full_unstemmed Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
title_short Malignant Hypertensive Retinopathy in an Infant with Mid-Aortic Occlusion
title_sort malignant hypertensive retinopathy in an infant with mid aortic occlusion
url http://dx.doi.org/10.1155/2016/8162687
work_keys_str_mv AT lawrencejoh malignanthypertensiveretinopathyinaninfantwithmidaorticocclusion
AT gauravbhardwaj malignanthypertensiveretinopathyinaninfantwithmidaorticocclusion
AT davidswinlaw malignanthypertensiveretinopathyinaninfantwithmidaorticocclusion
AT craigedonaldson malignanthypertensiveretinopathyinaninfantwithmidaorticocclusion