Resection of a conus medullaris hemangioblastoma: Case report

Background: Conus medullaris tumors are rare, as the majority of all spinal cord tumors occur in the cervical and thoracic regions. Hemangioblastomas of the spinal cord account for 3%–4% of all intramedullary spinal cord tumors and can be sporadic or associated with von Hippel-Lindau disease. There...

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Main Authors: Reinier Alvarez, Panagiotis Mastorakos, Prashant Chittiboina
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:Interdisciplinary Neurosurgery
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214751920304655
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author Reinier Alvarez
Panagiotis Mastorakos
Prashant Chittiboina
author_facet Reinier Alvarez
Panagiotis Mastorakos
Prashant Chittiboina
author_sort Reinier Alvarez
collection DOAJ
description Background: Conus medullaris tumors are rare, as the majority of all spinal cord tumors occur in the cervical and thoracic regions. Hemangioblastomas of the spinal cord account for 3%–4% of all intramedullary spinal cord tumors and can be sporadic or associated with von Hippel-Lindau disease. There are only fourteen cases of conus medullaris hemangioblastomas published in the literature, herein we present the fifteenth. Case description: A 44-year old male with von Hippel Lindau disease presented with worsening bilateral lower extremity weakness, gait imbalance as well as absent perineal and genital sensation with weak voluntary anal contraction. MRI demonstrated multiple stable spinal tumors and a 6 mm conus medullaris hemangioblastoma with growth and a new peri-tumoral cyst. The patient underwent uncomplicated surgical resection with appreciable improvement in perineal sensation and sphincteric control during post-operative course. Conclusions: Timely resection of conus medullaris tumors can provide symptomatic relief and prevent the progression of devastating neurological deficits. Careful microsurgical dissection with appropriate patient selection allows for safe resection of conus medullaris tumors.
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spelling doaj.art-36332a511d3946438e74492b201ac3792022-12-21T21:33:32ZengElsevierInterdisciplinary Neurosurgery2214-75192021-03-0123100904Resection of a conus medullaris hemangioblastoma: Case reportReinier Alvarez0Panagiotis Mastorakos1Prashant Chittiboina2Neurosurgery Unit for Pituitary and Inheritable Diseases, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States; Florida International University Herbert Wertheim College of Medicine, Miami, FL, United States; Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United StatesSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States; Department of Neurosurgery, University of Virginia, Charlottesville, VA, United StatesNeurosurgery Unit for Pituitary and Inheritable Diseases, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States; Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States; Corresponding author at: Neurosurgery Unit for Pituitary and Inheritable Diseases, National Institute of Neurological Diseases and Stroke, National Institutes of Health. 10 Center Drive, Room 3D20, Bethesda, MD 20892-1414, United States.Background: Conus medullaris tumors are rare, as the majority of all spinal cord tumors occur in the cervical and thoracic regions. Hemangioblastomas of the spinal cord account for 3%–4% of all intramedullary spinal cord tumors and can be sporadic or associated with von Hippel-Lindau disease. There are only fourteen cases of conus medullaris hemangioblastomas published in the literature, herein we present the fifteenth. Case description: A 44-year old male with von Hippel Lindau disease presented with worsening bilateral lower extremity weakness, gait imbalance as well as absent perineal and genital sensation with weak voluntary anal contraction. MRI demonstrated multiple stable spinal tumors and a 6 mm conus medullaris hemangioblastoma with growth and a new peri-tumoral cyst. The patient underwent uncomplicated surgical resection with appreciable improvement in perineal sensation and sphincteric control during post-operative course. Conclusions: Timely resection of conus medullaris tumors can provide symptomatic relief and prevent the progression of devastating neurological deficits. Careful microsurgical dissection with appropriate patient selection allows for safe resection of conus medullaris tumors.http://www.sciencedirect.com/science/article/pii/S2214751920304655Conus medullarisHemangioblastomaIntramedullary spinal cord tumorVon Hippel Lindau
spellingShingle Reinier Alvarez
Panagiotis Mastorakos
Prashant Chittiboina
Resection of a conus medullaris hemangioblastoma: Case report
Interdisciplinary Neurosurgery
Conus medullaris
Hemangioblastoma
Intramedullary spinal cord tumor
Von Hippel Lindau
title Resection of a conus medullaris hemangioblastoma: Case report
title_full Resection of a conus medullaris hemangioblastoma: Case report
title_fullStr Resection of a conus medullaris hemangioblastoma: Case report
title_full_unstemmed Resection of a conus medullaris hemangioblastoma: Case report
title_short Resection of a conus medullaris hemangioblastoma: Case report
title_sort resection of a conus medullaris hemangioblastoma case report
topic Conus medullaris
Hemangioblastoma
Intramedullary spinal cord tumor
Von Hippel Lindau
url http://www.sciencedirect.com/science/article/pii/S2214751920304655
work_keys_str_mv AT reinieralvarez resectionofaconusmedullarishemangioblastomacasereport
AT panagiotismastorakos resectionofaconusmedullarishemangioblastomacasereport
AT prashantchittiboina resectionofaconusmedullarishemangioblastomacasereport