Cargando…

Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report

BACKGROUND: Hemangioblastomas are benign tumors that develop in the central nervous system. They represent 1.5–2.5% of all intracranial tumors, and about 2–15% of all spinal cord tumors. They are highly associated with von Hippel–Lindau disease. CASE DESCRIPTION: A 36-year-old female presented with...

Descripción completa

Detalles Bibliográficos
Autores principales: Tirado-Ornelas, Héctor Alonso, Olivares-Peña, Jorge Luis, Olivares-Camacho, Jorge Luis, Santos-Franco, Jorge Arturo, Ochoa-González, Maurilio Vicente
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282796/
https://www.ncbi.nlm.nih.gov/pubmed/35855144
http://dx.doi.org/10.25259/SNI_525_2022
_version_ 1784747188011663360
author Tirado-Ornelas, Héctor Alonso
Olivares-Peña, Jorge Luis
Olivares-Camacho, Jorge Luis
Santos-Franco, Jorge Arturo
Ochoa-González, Maurilio Vicente
author_facet Tirado-Ornelas, Héctor Alonso
Olivares-Peña, Jorge Luis
Olivares-Camacho, Jorge Luis
Santos-Franco, Jorge Arturo
Ochoa-González, Maurilio Vicente
author_sort Tirado-Ornelas, Héctor Alonso
collection PubMed
description BACKGROUND: Hemangioblastomas are benign tumors that develop in the central nervous system. They represent 1.5–2.5% of all intracranial tumors, and about 2–15% of all spinal cord tumors. They are highly associated with von Hippel–Lindau disease. CASE DESCRIPTION: A 36-year-old female presented with a 4-year history of progressive right upper extremity distal weakness and cervical pain. The magnetic resonance imaging demonstrated a homogeneously, contrast enhancing intradural/intramedullary tumor at C6–C7 with perilesional edema and a syrinx accompanied by a cerebellar cyst with a mural nodule. Surgery included excision of the spinal lesion and decompression and excision of the cerebellar cyst and mural nodule (i.e., median suboccipital craniectomy and cervical C5–C7 laminectomy). CONCLUSION: Surgery is the gold standard treatment for symptomatic hemangioblastomas, and surgical approaches should minimize risk.
format Online
Article
Text
id pubmed-9282796
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Scientific Scholar
record_format MEDLINE/PubMed
spelling pubmed-92827962022-07-18 Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report Tirado-Ornelas, Héctor Alonso Olivares-Peña, Jorge Luis Olivares-Camacho, Jorge Luis Santos-Franco, Jorge Arturo Ochoa-González, Maurilio Vicente Surg Neurol Int Case Report BACKGROUND: Hemangioblastomas are benign tumors that develop in the central nervous system. They represent 1.5–2.5% of all intracranial tumors, and about 2–15% of all spinal cord tumors. They are highly associated with von Hippel–Lindau disease. CASE DESCRIPTION: A 36-year-old female presented with a 4-year history of progressive right upper extremity distal weakness and cervical pain. The magnetic resonance imaging demonstrated a homogeneously, contrast enhancing intradural/intramedullary tumor at C6–C7 with perilesional edema and a syrinx accompanied by a cerebellar cyst with a mural nodule. Surgery included excision of the spinal lesion and decompression and excision of the cerebellar cyst and mural nodule (i.e., median suboccipital craniectomy and cervical C5–C7 laminectomy). CONCLUSION: Surgery is the gold standard treatment for symptomatic hemangioblastomas, and surgical approaches should minimize risk. Scientific Scholar 2022-07-08 /pmc/articles/PMC9282796/ /pubmed/35855144 http://dx.doi.org/10.25259/SNI_525_2022 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Tirado-Ornelas, Héctor Alonso
Olivares-Peña, Jorge Luis
Olivares-Camacho, Jorge Luis
Santos-Franco, Jorge Arturo
Ochoa-González, Maurilio Vicente
Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title_full Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title_fullStr Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title_full_unstemmed Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title_short Intramedullary cervical spinal cord and cerebellar hemangioblastoma: A case report
title_sort intramedullary cervical spinal cord and cerebellar hemangioblastoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282796/
https://www.ncbi.nlm.nih.gov/pubmed/35855144
http://dx.doi.org/10.25259/SNI_525_2022
work_keys_str_mv AT tiradoornelashectoralonso intramedullarycervicalspinalcordandcerebellarhemangioblastomaacasereport
AT olivarespenajorgeluis intramedullarycervicalspinalcordandcerebellarhemangioblastomaacasereport
AT olivarescamachojorgeluis intramedullarycervicalspinalcordandcerebellarhemangioblastomaacasereport
AT santosfrancojorgearturo intramedullarycervicalspinalcordandcerebellarhemangioblastomaacasereport
AT ochoagonzalezmauriliovicente intramedullarycervicalspinalcordandcerebellarhemangioblastomaacasereport