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Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome
We report the case of a forty-nine year-old Native American female who presented with two-month history of headaches and unsteady gait. MRI brain showed a 6.5 cm by 5 cm enhancing dural-based mass with leftward midline shift. She was taken to the operating room for gross-total tumor resection. Patho...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JSCR Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862244/ https://www.ncbi.nlm.nih.gov/pubmed/24960680 http://dx.doi.org/10.1093/jscr/2012.6.11 |
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author | Kaloostian, PE Taylor, CL |
author_facet | Kaloostian, PE Taylor, CL |
author_sort | Kaloostian, PE |
collection | PubMed |
description | We report the case of a forty-nine year-old Native American female who presented with two-month history of headaches and unsteady gait. MRI brain showed a 6.5 cm by 5 cm enhancing dural-based mass with leftward midline shift. She was taken to the operating room for gross-total tumor resection. Pathology was supratentorial haemangioblastoma. This is the first known case of a supratentorial dural-based haemangioblastoma in a person of Native American descent. We review the literature and describe the unique characteristics of this tumor. |
format | Online Article Text |
id | pubmed-3862244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | JSCR Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38622442013-12-18 Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome Kaloostian, PE Taylor, CL J Surg Case Rep Neurosurgery We report the case of a forty-nine year-old Native American female who presented with two-month history of headaches and unsteady gait. MRI brain showed a 6.5 cm by 5 cm enhancing dural-based mass with leftward midline shift. She was taken to the operating room for gross-total tumor resection. Pathology was supratentorial haemangioblastoma. This is the first known case of a supratentorial dural-based haemangioblastoma in a person of Native American descent. We review the literature and describe the unique characteristics of this tumor. JSCR Publishing Ltd 2012-06-01 /pmc/articles/PMC3862244/ /pubmed/24960680 http://dx.doi.org/10.1093/jscr/2012.6.11 Text en © JSCR |
spellingShingle | Neurosurgery Kaloostian, PE Taylor, CL Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title | Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title_full | Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title_fullStr | Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title_full_unstemmed | Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title_short | Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome |
title_sort | supratentorial dural-based haemangioblastoma in a native american patient without von hippel lindau syndrome |
topic | Neurosurgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862244/ https://www.ncbi.nlm.nih.gov/pubmed/24960680 http://dx.doi.org/10.1093/jscr/2012.6.11 |
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