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Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report

BACKGROUND: Perthes Syndrome (Traumatic asphyxia) is rare, which is caused by sudden compressive chest trauma and characterized by subconjunctival hemorrhage, facial edema, craniocervical cyanosis, and petechiae on the upper chest and face. CASE PRESENTATION: We present the case of a 4-year-old Cauc...

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Detalles Bibliográficos
Autores principales: Senoglu, Mehmet, Senoglu, Nimet, Oksuz, Hafize, Ispir, Gokhan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440364/
https://www.ncbi.nlm.nih.gov/pubmed/18577198
http://dx.doi.org/10.1186/1757-1626-1-17
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author Senoglu, Mehmet
Senoglu, Nimet
Oksuz, Hafize
Ispir, Gokhan
author_facet Senoglu, Mehmet
Senoglu, Nimet
Oksuz, Hafize
Ispir, Gokhan
author_sort Senoglu, Mehmet
collection PubMed
description BACKGROUND: Perthes Syndrome (Traumatic asphyxia) is rare, which is caused by sudden compressive chest trauma and characterized by subconjunctival hemorrhage, facial edema, craniocervical cyanosis, and petechiae on the upper chest and face. CASE PRESENTATION: We present the case of a 4-year-old Caucasian girl who developed traumatic asphyxia associated with intramedullary spinal cord hemorrhage following thoracic compression. CONCLUSION: We have not found the association of Perthes syndrome with intramedullary spinal cord hemorrhage described in the medical literature. To our knowledge, the current case is the first report of Perthes Syndrome associated with intramedullary spinal cord hemorrhage.
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spelling pubmed-24403642008-06-27 Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report Senoglu, Mehmet Senoglu, Nimet Oksuz, Hafize Ispir, Gokhan Cases J Case Report BACKGROUND: Perthes Syndrome (Traumatic asphyxia) is rare, which is caused by sudden compressive chest trauma and characterized by subconjunctival hemorrhage, facial edema, craniocervical cyanosis, and petechiae on the upper chest and face. CASE PRESENTATION: We present the case of a 4-year-old Caucasian girl who developed traumatic asphyxia associated with intramedullary spinal cord hemorrhage following thoracic compression. CONCLUSION: We have not found the association of Perthes syndrome with intramedullary spinal cord hemorrhage described in the medical literature. To our knowledge, the current case is the first report of Perthes Syndrome associated with intramedullary spinal cord hemorrhage. BioMed Central 2008-06-13 /pmc/articles/PMC2440364/ /pubmed/18577198 http://dx.doi.org/10.1186/1757-1626-1-17 Text en Copyright © 2008 Senoglu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Senoglu, Mehmet
Senoglu, Nimet
Oksuz, Hafize
Ispir, Gokhan
Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title_full Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title_fullStr Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title_full_unstemmed Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title_short Perthes Syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
title_sort perthes syndrome associated with intramedullary spinal cord hemorrhage in a 4-year-old child: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440364/
https://www.ncbi.nlm.nih.gov/pubmed/18577198
http://dx.doi.org/10.1186/1757-1626-1-17
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