Ganglioneuroblastoma of the posterior mediastinum: a case report
<p>Abstract</p> <p>Introduction</p> <p>Ganglioneuroblastoma is a rare peripheral neuroblastic tumor that is derived from developing neuronal cells of the sympathetic nervous system, and is found mostly, but not exclusively, in babies and young children.</p> <p&...
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doaj-b544659c09b7495980f782d0cac4e2092020-11-25T02:33:35ZengBMCJournal of Medical Case Reports1752-19472011-07-015132210.1186/1752-1947-5-322Ganglioneuroblastoma of the posterior mediastinum: a case reportBawany Samira AFatimi Saulat HAshfaq Awais<p>Abstract</p> <p>Introduction</p> <p>Ganglioneuroblastoma is a rare peripheral neuroblastic tumor that is derived from developing neuronal cells of the sympathetic nervous system, and is found mostly, but not exclusively, in babies and young children.</p> <p>Case presentation</p> <p>To the best of our knowledge, there have been no previously reported cases of ganglioneuroblastoma of the mediastinum from Pakistan. We present a case of ganglioneuroblastoma in an eight-year-old Pakistani Sindhi boy incidentally found to have a large posterior mediastinal mass that on biopsy initially looked like ganglioneuroma. He underwent successful excision of the mediastinal mass and remained stable post-operatively. Final pathology findings showed a ganglioneuroblastoma. He has remained free of symptoms on long-term follow-up.</p> <p>Conclusions</p> <p>The rarity of this tumor along with its almost exclusive occurrence in the pediatric population necessitates a thorough investigation of patients presenting with a symptomatic mass.</p> http://www.jmedicalcasereports.com/content/5/1/322 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Bawany Samira A Fatimi Saulat H Ashfaq Awais |
spellingShingle |
Bawany Samira A Fatimi Saulat H Ashfaq Awais Ganglioneuroblastoma of the posterior mediastinum: a case report Journal of Medical Case Reports |
author_facet |
Bawany Samira A Fatimi Saulat H Ashfaq Awais |
author_sort |
Bawany Samira A |
title |
Ganglioneuroblastoma of the posterior mediastinum: a case report |
title_short |
Ganglioneuroblastoma of the posterior mediastinum: a case report |
title_full |
Ganglioneuroblastoma of the posterior mediastinum: a case report |
title_fullStr |
Ganglioneuroblastoma of the posterior mediastinum: a case report |
title_full_unstemmed |
Ganglioneuroblastoma of the posterior mediastinum: a case report |
title_sort |
ganglioneuroblastoma of the posterior mediastinum: a case report |
publisher |
BMC |
series |
Journal of Medical Case Reports |
issn |
1752-1947 |
publishDate |
2011-07-01 |
description |
<p>Abstract</p> <p>Introduction</p> <p>Ganglioneuroblastoma is a rare peripheral neuroblastic tumor that is derived from developing neuronal cells of the sympathetic nervous system, and is found mostly, but not exclusively, in babies and young children.</p> <p>Case presentation</p> <p>To the best of our knowledge, there have been no previously reported cases of ganglioneuroblastoma of the mediastinum from Pakistan. We present a case of ganglioneuroblastoma in an eight-year-old Pakistani Sindhi boy incidentally found to have a large posterior mediastinal mass that on biopsy initially looked like ganglioneuroma. He underwent successful excision of the mediastinal mass and remained stable post-operatively. Final pathology findings showed a ganglioneuroblastoma. He has remained free of symptoms on long-term follow-up.</p> <p>Conclusions</p> <p>The rarity of this tumor along with its almost exclusive occurrence in the pediatric population necessitates a thorough investigation of patients presenting with a symptomatic mass.</p> |
url |
http://www.jmedicalcasereports.com/content/5/1/322 |
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