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Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia
Haemangioblastomas are uncommon tumours that usually occur in the cerebellum and, less commonly, in the intramedullary spinal cord. The extramedullary spinal canal is an uncommon location for these tumours. Also haemangioblastoma at this site is not known to be associated with polycythemia. We prese...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241257/ https://www.ncbi.nlm.nih.gov/pubmed/25431722 http://dx.doi.org/10.1155/2014/798620 |
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author | Law, Eric K. C. Lee, Ryan K. L. Griffith, James F. Siu, Deyond Y. W. Ng, Ho Keung |
author_facet | Law, Eric K. C. Lee, Ryan K. L. Griffith, James F. Siu, Deyond Y. W. Ng, Ho Keung |
author_sort | Law, Eric K. C. |
collection | PubMed |
description | Haemangioblastomas are uncommon tumours that usually occur in the cerebellum and, less commonly, in the intramedullary spinal cord. The extramedullary spinal canal is an uncommon location for these tumours. Also haemangioblastoma at this site is not known to be associated with polycythemia. We present the clinical, imaging, and histological findings of an adult patient with extramedullary spinal haemangioblastoma and reactive polycythemia. Radiography and computed tomography (CT) revealed a medium-sized tumour that most likely arose from an extramedullary spinal nerve root. This tumour appeared to be slow growing as evidenced by the accompanying well-defined bony resorption with a sclerotic rim and mild neural foraminal widening. Magnetic resonance imaging revealed prominent flow voids consistent with tumoural hypervascularity. CT-guided biopsy was performed. Although preoperative angiographic embolisation was technically successful, excessive intraoperative tumour bleeding necessitated tumour debulking rather than complete tumour resection. Histology of the resected specimen revealed haemangioblastoma. Seven months postoperatively, the patients back pain and polycythemia have resolved. |
format | Online Article Text |
id | pubmed-4241257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42412572014-11-27 Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia Law, Eric K. C. Lee, Ryan K. L. Griffith, James F. Siu, Deyond Y. W. Ng, Ho Keung Case Rep Radiol Case Report Haemangioblastomas are uncommon tumours that usually occur in the cerebellum and, less commonly, in the intramedullary spinal cord. The extramedullary spinal canal is an uncommon location for these tumours. Also haemangioblastoma at this site is not known to be associated with polycythemia. We present the clinical, imaging, and histological findings of an adult patient with extramedullary spinal haemangioblastoma and reactive polycythemia. Radiography and computed tomography (CT) revealed a medium-sized tumour that most likely arose from an extramedullary spinal nerve root. This tumour appeared to be slow growing as evidenced by the accompanying well-defined bony resorption with a sclerotic rim and mild neural foraminal widening. Magnetic resonance imaging revealed prominent flow voids consistent with tumoural hypervascularity. CT-guided biopsy was performed. Although preoperative angiographic embolisation was technically successful, excessive intraoperative tumour bleeding necessitated tumour debulking rather than complete tumour resection. Histology of the resected specimen revealed haemangioblastoma. Seven months postoperatively, the patients back pain and polycythemia have resolved. Hindawi Publishing Corporation 2014 2014-11-06 /pmc/articles/PMC4241257/ /pubmed/25431722 http://dx.doi.org/10.1155/2014/798620 Text en Copyright © 2014 Eric K. C. Law et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Law, Eric K. C. Lee, Ryan K. L. Griffith, James F. Siu, Deyond Y. W. Ng, Ho Keung Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title | Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title_full | Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title_fullStr | Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title_full_unstemmed | Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title_short | Spinal Nerve Root Haemangioblastoma Associated with Reactive Polycythemia |
title_sort | spinal nerve root haemangioblastoma associated with reactive polycythemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241257/ https://www.ncbi.nlm.nih.gov/pubmed/25431722 http://dx.doi.org/10.1155/2014/798620 |
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