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"Rabbit Ear" scalp deformity caused by massive subdural effusion in infant following bilateral burr-hole drainage.

作者信息

Satyarthee Guru Dutta, Pankaj Dawar, Sharma B S

机构信息

Department of Neurosurgery, All India Institute of Medical Sciences and Associated Jai Prakash Narayan Apex Trauma Centre, New Delhi, India.

出版信息

J Pediatr Neurosci. 2013 Sep;8(3):235-8. doi: 10.4103/1817-1745.123690.

Abstract

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/677e/3888045/6cb2b5148f8c/JPN-8-235-g001.jpg

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