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“Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage
Subdural effusion (SDE) in an infant is a rare clinical scenario, which may be secondary to a variety of etiologies. Massive SDE is an extremely rare complication of head injury. It usually runs a self-limiting course. Though neurosurgical intervention is occasionally needed, different methods of su...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888045/ https://www.ncbi.nlm.nih.gov/pubmed/24470822 http://dx.doi.org/10.4103/1817-1745.123690 |
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author | Satyarthee, Guru Dutta Pankaj, Dawar Sharma, B. S. |
author_facet | Satyarthee, Guru Dutta Pankaj, Dawar Sharma, B. S. |
author_sort | Satyarthee, Guru Dutta |
collection | PubMed |
description | Subdural effusion (SDE) in an infant is a rare clinical scenario, which may be secondary to a variety of etiologies. Massive SDE is an extremely rare complication of head injury. It usually runs a self-limiting course. Though neurosurgical intervention is occasionally needed, different methods of surgical procedure for management includes burr-hole alone, burr-holes with subdural drain placement, twist drill craniotomy with drain and even craniotomy. The authors report a rare case of progressive massive SDE, which despite bilateral burr-hole placement and drainage failed and presented with visual deterioration and massive bulge of scalp at burr-hole sites producing rabbit ear sign in a 10 month old infant. Ultimately cystoperitoneal shunt was carried out in a desperate attempt to prevent impending rupture of scalp sutures at sites of previous burr-hole placement. Astonishingly not only complete resolution of hygroma, but visual recovery also took place. Patient is doing well at 6 months following shunt with regaining normal vision and appropriate developmental milestones. A magnetic resonance imaging scan of brain at last follow-up revealed mild ventriculomegaly with subduro-peritoneal shunt in situ and rest of brain was unremarkable. Such cases have not been reported in literature until date. |
format | Online Article Text |
id | pubmed-3888045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38880452014-01-27 “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage Satyarthee, Guru Dutta Pankaj, Dawar Sharma, B. S. J Pediatr Neurosci Case Report Subdural effusion (SDE) in an infant is a rare clinical scenario, which may be secondary to a variety of etiologies. Massive SDE is an extremely rare complication of head injury. It usually runs a self-limiting course. Though neurosurgical intervention is occasionally needed, different methods of surgical procedure for management includes burr-hole alone, burr-holes with subdural drain placement, twist drill craniotomy with drain and even craniotomy. The authors report a rare case of progressive massive SDE, which despite bilateral burr-hole placement and drainage failed and presented with visual deterioration and massive bulge of scalp at burr-hole sites producing rabbit ear sign in a 10 month old infant. Ultimately cystoperitoneal shunt was carried out in a desperate attempt to prevent impending rupture of scalp sutures at sites of previous burr-hole placement. Astonishingly not only complete resolution of hygroma, but visual recovery also took place. Patient is doing well at 6 months following shunt with regaining normal vision and appropriate developmental milestones. A magnetic resonance imaging scan of brain at last follow-up revealed mild ventriculomegaly with subduro-peritoneal shunt in situ and rest of brain was unremarkable. Such cases have not been reported in literature until date. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3888045/ /pubmed/24470822 http://dx.doi.org/10.4103/1817-1745.123690 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Satyarthee, Guru Dutta Pankaj, Dawar Sharma, B. S. “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title | “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title_full | “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title_fullStr | “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title_full_unstemmed | “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title_short | “Rabbit Ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
title_sort | “rabbit ear” scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888045/ https://www.ncbi.nlm.nih.gov/pubmed/24470822 http://dx.doi.org/10.4103/1817-1745.123690 |
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