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Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review

Non traumatic spontaneous epidural Haematoma is a rare and often unmentioned complication of sickle cell disease. It is often associated with skull bone infarction. We report an eighteen year old boy with sickle cell anaemia who developed persistence headache during a vaso-occlusive crisis. Brain co...

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Autores principales: Babatola, Bankole O., Salman, Yusuf A., Abiola, Asha M., Okezie, Kanu O., Oladele, Arigbabu S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673360/
https://www.ncbi.nlm.nih.gov/pubmed/23741596
http://dx.doi.org/10.4103/2006-8808.110271
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author Babatola, Bankole O.
Salman, Yusuf A.
Abiola, Asha M.
Okezie, Kanu O.
Oladele, Arigbabu S.
author_facet Babatola, Bankole O.
Salman, Yusuf A.
Abiola, Asha M.
Okezie, Kanu O.
Oladele, Arigbabu S.
author_sort Babatola, Bankole O.
collection PubMed
description Non traumatic spontaneous epidural Haematoma is a rare and often unmentioned complication of sickle cell disease. It is often associated with skull bone infarction. We report an eighteen year old boy with sickle cell anaemia who developed persistence headache during a vaso-occlusive crisis. Brain computed tomography (CT) revealed a right frontal epidural Haematoma (EDH) compressing on the brain. No other etiologic factor was identified. A right frontal craniotomy and evacuation of the Haematoma was performed and he made good recovery. The possible pathogeneses of this rare condition are discussed.
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spelling pubmed-36733602013-06-05 Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review Babatola, Bankole O. Salman, Yusuf A. Abiola, Asha M. Okezie, Kanu O. Oladele, Arigbabu S. J Surg Tech Case Rep Case Report Non traumatic spontaneous epidural Haematoma is a rare and often unmentioned complication of sickle cell disease. It is often associated with skull bone infarction. We report an eighteen year old boy with sickle cell anaemia who developed persistence headache during a vaso-occlusive crisis. Brain computed tomography (CT) revealed a right frontal epidural Haematoma (EDH) compressing on the brain. No other etiologic factor was identified. A right frontal craniotomy and evacuation of the Haematoma was performed and he made good recovery. The possible pathogeneses of this rare condition are discussed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3673360/ /pubmed/23741596 http://dx.doi.org/10.4103/2006-8808.110271 Text en Copyright: © Journal of Surgical Technique and Case Report 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
Babatola, Bankole O.
Salman, Yusuf A.
Abiola, Asha M.
Okezie, Kanu O.
Oladele, Arigbabu S.
Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title_full Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title_fullStr Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title_full_unstemmed Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title_short Spontaneous Epidural Haematoma in Sickle Cell Anaemia: Case Report and Literature Review
title_sort spontaneous epidural haematoma in sickle cell anaemia: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673360/
https://www.ncbi.nlm.nih.gov/pubmed/23741596
http://dx.doi.org/10.4103/2006-8808.110271
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