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Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study

INTRODUCTION: Contrary to some earlier teachings that central nervous system (CNS) tumours are uncommon in black children, these neoplasms are the fourth most common paediatric tumours in Ibadan. Our centre is the major referral centre for CNS tumours in Nigeria. The last major study of paediatric C...

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Autores principales: Ogun, Gabriel Olabiyi, Adeleye, Amos Olufemi, Babatunde, Taiwo Olabimpe, Ogun, Olufunmilola Abimbola, Salami, Ayodeji, Brown, Biobele Jotham, Akang, Effiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992396/
https://www.ncbi.nlm.nih.gov/pubmed/27583098
http://dx.doi.org/10.11604/pamj.2016.24.34.9344
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author Ogun, Gabriel Olabiyi
Adeleye, Amos Olufemi
Babatunde, Taiwo Olabimpe
Ogun, Olufunmilola Abimbola
Salami, Ayodeji
Brown, Biobele Jotham
Akang, Effiong
author_facet Ogun, Gabriel Olabiyi
Adeleye, Amos Olufemi
Babatunde, Taiwo Olabimpe
Ogun, Olufunmilola Abimbola
Salami, Ayodeji
Brown, Biobele Jotham
Akang, Effiong
author_sort Ogun, Gabriel Olabiyi
collection PubMed
description INTRODUCTION: Contrary to some earlier teachings that central nervous system (CNS) tumours are uncommon in black children, these neoplasms are the fourth most common paediatric tumours in Ibadan. Our centre is the major referral centre for CNS tumours in Nigeria. The last major study of paediatric CNS neoplasms from Ibadan was in 1985. An update of the data on paediatric CNS neoplasms at our centre is presented. METHODS: A retrospective review of all histologically diagnosed CNS tumours in children (0-14 years) from January 2001 to December 2010 from the database of the Department of Pathology, University College Hospital, Ibadan, Nigeria was done. The cases were classified using the 2007 WHO Classification of Tumours of the Central Nervous System and were also based on their supratentorial and infratentorial locations. RESULTS: Seventy-seven tumours, 44 in males, were included in the study. Astrocytic tumour comprised 20 cases, embryonal tumours 15, ependymal tumours 15, germ cell tumours 6, sellar tumours (all craniopharyngiomas) 9 and other histological types- 12 cases. Thirty-seven were WHO Grade 1, eleven Grade 2, ten Grade 3 and nineteen Grade 4 neoplasms. Thirty-six cases were supratentorial and thirty-eight were infratentorial in location. The most common tumours in this series were pilocytic astrocytomas, medulloblastomas, craniopharyngiomas and ependymomas in that order. CONCLUSION: Childhood CNS tumours are being increasingly diagnosed in our centre. This is largely explained by the recent expansion of the available neurosurgical services.
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spelling pubmed-49923962016-08-31 Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study Ogun, Gabriel Olabiyi Adeleye, Amos Olufemi Babatunde, Taiwo Olabimpe Ogun, Olufunmilola Abimbola Salami, Ayodeji Brown, Biobele Jotham Akang, Effiong Pan Afr Med J Research INTRODUCTION: Contrary to some earlier teachings that central nervous system (CNS) tumours are uncommon in black children, these neoplasms are the fourth most common paediatric tumours in Ibadan. Our centre is the major referral centre for CNS tumours in Nigeria. The last major study of paediatric CNS neoplasms from Ibadan was in 1985. An update of the data on paediatric CNS neoplasms at our centre is presented. METHODS: A retrospective review of all histologically diagnosed CNS tumours in children (0-14 years) from January 2001 to December 2010 from the database of the Department of Pathology, University College Hospital, Ibadan, Nigeria was done. The cases were classified using the 2007 WHO Classification of Tumours of the Central Nervous System and were also based on their supratentorial and infratentorial locations. RESULTS: Seventy-seven tumours, 44 in males, were included in the study. Astrocytic tumour comprised 20 cases, embryonal tumours 15, ependymal tumours 15, germ cell tumours 6, sellar tumours (all craniopharyngiomas) 9 and other histological types- 12 cases. Thirty-seven were WHO Grade 1, eleven Grade 2, ten Grade 3 and nineteen Grade 4 neoplasms. Thirty-six cases were supratentorial and thirty-eight were infratentorial in location. The most common tumours in this series were pilocytic astrocytomas, medulloblastomas, craniopharyngiomas and ependymomas in that order. CONCLUSION: Childhood CNS tumours are being increasingly diagnosed in our centre. This is largely explained by the recent expansion of the available neurosurgical services. The African Field Epidemiology Network 2016-05-09 /pmc/articles/PMC4992396/ /pubmed/27583098 http://dx.doi.org/10.11604/pamj.2016.24.34.9344 Text en © Gabriel Olabiyi Ogun et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ogun, Gabriel Olabiyi
Adeleye, Amos Olufemi
Babatunde, Taiwo Olabimpe
Ogun, Olufunmilola Abimbola
Salami, Ayodeji
Brown, Biobele Jotham
Akang, Effiong
Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title_full Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title_fullStr Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title_full_unstemmed Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title_short Central nervous system tumours in children in Ibadan, Nigeria: a histopathologic study
title_sort central nervous system tumours in children in ibadan, nigeria: a histopathologic study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992396/
https://www.ncbi.nlm.nih.gov/pubmed/27583098
http://dx.doi.org/10.11604/pamj.2016.24.34.9344
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