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Primary spinal primitive neuroectodermal tumour – a case report
Primitive neuroectodermal tumours (PNET) are aggressive childhood malignancies and offer a significant challenge to treatment. A two years old female child presented with weakness both lower limbs. Preoperative MRI of the spine and paravertebral regionIso – hyper intense posterior placed extradural...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Academy of Neurosciences
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117112/ https://www.ncbi.nlm.nih.gov/pubmed/25206019 http://dx.doi.org/10.5214/ans.0972.7531.200211 |
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author | Venkataraman, Sundar Pandian, Chelladurai Kumar, Suresh A. |
author_facet | Venkataraman, Sundar Pandian, Chelladurai Kumar, Suresh A. |
author_sort | Venkataraman, Sundar |
collection | PubMed |
description | Primitive neuroectodermal tumours (PNET) are aggressive childhood malignancies and offer a significant challenge to treatment. A two years old female child presented with weakness both lower limbs. Preoperative MRI of the spine and paravertebral regionIso – hyper intense posterior placed extradural lesion, non contrast enhancing from D11-L2 levels with cord compression D9 to L3 laminectomy done. Granulation tissue found from D11 to L2. with cord compression. The granulation tissue removed in toto. The pathological findings were consistent with PNET. Post operative neurological improvement was minimal. Cranial screening ruled out any intracranialtumour. Hence a diagnosis of primary spinal PNET was made. A review of the literature shows that only 19 cases of primary intraspinal PNETs have been reported to date and the present case extradural in location. Primary intraspinal PNETs are rare tumors and carry a poor prognosis. |
format | Online Article Text |
id | pubmed-4117112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Indian Academy of Neurosciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-41171122014-09-09 Primary spinal primitive neuroectodermal tumour – a case report Venkataraman, Sundar Pandian, Chelladurai Kumar, Suresh A. Ann Neurosci Case Report Primitive neuroectodermal tumours (PNET) are aggressive childhood malignancies and offer a significant challenge to treatment. A two years old female child presented with weakness both lower limbs. Preoperative MRI of the spine and paravertebral regionIso – hyper intense posterior placed extradural lesion, non contrast enhancing from D11-L2 levels with cord compression D9 to L3 laminectomy done. Granulation tissue found from D11 to L2. with cord compression. The granulation tissue removed in toto. The pathological findings were consistent with PNET. Post operative neurological improvement was minimal. Cranial screening ruled out any intracranialtumour. Hence a diagnosis of primary spinal PNET was made. A review of the literature shows that only 19 cases of primary intraspinal PNETs have been reported to date and the present case extradural in location. Primary intraspinal PNETs are rare tumors and carry a poor prognosis. Indian Academy of Neurosciences 2013-04 /pmc/articles/PMC4117112/ /pubmed/25206019 http://dx.doi.org/10.5214/ans.0972.7531.200211 Text en Copyright © 2013, Annals of Neurosciences |
spellingShingle | Case Report Venkataraman, Sundar Pandian, Chelladurai Kumar, Suresh A. Primary spinal primitive neuroectodermal tumour – a case report |
title | Primary spinal primitive neuroectodermal tumour – a case report |
title_full | Primary spinal primitive neuroectodermal tumour – a case report |
title_fullStr | Primary spinal primitive neuroectodermal tumour – a case report |
title_full_unstemmed | Primary spinal primitive neuroectodermal tumour – a case report |
title_short | Primary spinal primitive neuroectodermal tumour – a case report |
title_sort | primary spinal primitive neuroectodermal tumour – a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117112/ https://www.ncbi.nlm.nih.gov/pubmed/25206019 http://dx.doi.org/10.5214/ans.0972.7531.200211 |
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